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What is a chromosome DNA and genes



What is a chromosome?

What is a chromosome? Everything we need to know about chromosomes . Our genetic information is stored in 23 pairs of chromosomes that vary greatly in size and shape. Join us to learn more about chromosomes.

What is a chromosome?

Chromosomes are string-like structures located in the nucleus of plant and animal cells. Each chromosome consists of a protein and a molecule of deoxyribonucleic acid (DNA). DNA is passed from parent to offspring and contains specific instructions that make each living thing unique.

The term chromosome (colored body) comes from the Greek words color (chroma) and body (soma). Scientists gave this name to chromosomes because they are structures or cell bodies that are strongly colored by special dyes used in research. What do chromosomes do?

The unique structure of chromosomes keeps DNA tightly wrapped around coil-like proteins called histones. Without such packaging, DNA molecules are too long to fit inside cells. For example, if all the DNA molecules in a human cell were separated from their histones and strung together, they would be 6 feet (1.8 meters) long.

For an organism to grow and function properly, cells must constantly divide to produce new cells to replace old cells. During cell division, it is essential that DNA remains intact and is equally distributed between cells. Chromosomes are a key part of the process that ensures that DNA is accurately copied and distributed during cell division. However, in rare cases, mistakes also occur.

Changes in the number or structure of chromosomes in new cells can lead to serious problems. For example, in humans, some types of leukemia and some other cancers are caused by defective chromosomes, which are made up of joined pieces of broken chromosomes.

It is also very important that reproductive cells such as eggs and sperm contain the correct number of chromosomes and that their chromosome structure is correct. Otherwise, the growth and development of the resulting children may be disturbed. For example, people with Down syndrome have 3 copies of chromosome 21 instead of the two copies that other people have.

Chromosome DNA and genes

Do all living things have the same type of chromosomes?

The number and shape of chromosomes vary among living organisms. Most bacteria have one or two circular chromosomes. Humans, along with other animals and plants, have linear chromosomes that are located in pairs in the nucleus of cells.

The only human cells that do not contain a pair of chromosomes are the reproductive cells, or gametes, which carry only one copy of each chromosome. When two gametes fuse, they become a single cell that contains two copies of each chromosome. This cell then divides and the resulting cells divide many times, eventually forming an adult that has a complete set of chromosome pairs in almost all of its cells.

In addition to the linear chromosomes found in the cell nucleus, human cells, and other complex organisms have a much smaller type of chromosome that resembles what is found in bacteria. This circular chromosome is found in mitochondria, which are structures outside the nucleus that act as the powerhouse of the cell.

Scientists think that in the past, mitochondria were independent bacteria with the ability to convert oxygen into energy. When these bacteria attacked cells that could not use oxygen, the cells kept them, and over time, the bacteria evolved into today’s mitochondria.

Chromosome structure

What is a centromere?

The compact region of linear chromosomes is called the centromere. Although this compaction is called a centromere (which refers to the center), it is usually not located exactly in the center of the chromosome, and in some cases, it is located almost at the end of the chromosome. The regions on both sides of the centromere are called chromosome arms.

The centromere helps to place the chromosomes in the right position in the cell during the complex process of cell division. Chromosomes are copied before a new cell is produced, and the centromere serves as the junction for the two halves of each replicated chromosome, known as sister chromatids.

What is chromatid?

A chromatid is one of the two identical halves of a replicated chromosome. During cell division, first, the chromosomes go through the replication process so that each daughter cell receives a complete set of chromosomes. Following DNA replication, the chromosome consists of two identical structures called sister chromatids, which are joined together at the centromere.

Chromosome structure

In simpler terms, during DNA division, when a cell divides, the cell must copy its DNA and then transfer half of it to one cell and half to another cell. As you know, DNA is arranged in chromosomes, so when a chromosome replicates or makes a copy of itself, the resulting genetic material is put together as two chromosomes, called chromatids. Then in the next stage of cell division, when the DNA is transferred to two daughter cells, one of the chromatids is transferred to each of the two cells; Therefore, a chromatid is a copy of a chromosome after DNA replication.

What is a telomere?

Telomeres are repetitive segments of DNA located at the ends of linear chromosomes. They protect the ends of chromosomes the way a shoelace protects a shoelace from unraveling.

In many types of cells, telomeres lose a portion of their DNA each time the cell divides. Eventually, when all the telomeric DNA is gone, the cell can no longer reproduce and dies. White blood cells and other cells that have a very high rate of cell division have a special enzyme that prevents their chromosomes from losing their telomeres. Because they maintain their telomeres, they usually live longer than other cells. Telomeres also play a role in cancer. Chromosomes in malignant cells usually do not lose their telomeres, contributing to the uncontrolled growth that makes cancer so devastating.

Read More: Why was the human genome never completed?

The number of human chromosomes

Humans have 23 pairs of chromosomes and a total of 46 chromosomes. All plants and animals have a specific number of chromosomes. For example, a fruit fly has four pairs of chromosomes, while a rice plant has 12 and a dog has 39.

What is a karyotype?

A karyotype is a picture of a person’s chromosomes. To produce this image, the chromosomes are separated, stained, and examined under a microscope. This is usually done using the chromosomes in the white blood cells. The chromosomes are imaged under a microscope and then cut, and the chromosomes are sorted by size from largest to smallest. An experienced cytogeneticist can identify missing or extra parts of chromosomes. The karyotype of a male is shown in the figure below.

How are chromosomes numbered?

Each chromosome is assigned a specific number based on its size. The largest chromosome is chromosome number one. For example, in humans, chromosome number 18 is one of the smallest chromosomes.

How are chromosomes inherited?

In humans and most other complex organisms, one copy of each chromosome is inherited from the female parent and the other from the male parent. This explains why children inherit some traits from the mother and others from the father. The inheritance pattern of the small circular chromosome present in mitochondria is different. Only egg cells (and not sperm cells) retain their mitochondria during fertilization; Therefore, mitochondrial DNA is always inherited from the female parent. In humans, a few diseases, including some forms of hearing impairment and diabetes, have been linked to mitochondrial DNA.

Are male chromosomes different from female chromosomes?

Yes, they differ in a pair of chromosomes known as sex chromosomes. Females have two X chromosomes in their cells, while males have one X chromosome and one Y chromosome. Inheriting extra or fewer copies of sex chromosomes can lead to serious problems. For example, women with extra copies of the X chromosome tend to be taller than average, and some have mental retardation. Men with more than one X chromosome have Klinefelter syndrome, a condition characterized by tall stature and often impaired fertility. Another syndrome caused by an imbalance in the number of sex chromosomes is Turner’s syndrome. Women with Turner syndrome have only one X chromosome. They are very short, usually do not reach puberty, and some may have heart or kidney problems.

کروموزوم X و Y

Facts about X chromosome and Y chromosome

1. In the nucleus of each cell, DNA is packaged in string-like structures called chromosomes.

2. Most human cells have 23 pairs of chromosomes. One set of chromosomes comes from the mother, while the other set is inherited from the father. The 23rd pair are sex chromosomes, while the other 22 pairs are called autosomes.

3. Normally, people who are biologically female have two X chromosomes, while people who are biologically male have one X chromosome and one Y chromosome. Although there are exceptions to this rule.

4. From the point of view of female biology, people inherit one X chromosome from their father and another X chromosome from their mother. Biologically male people always get their X chromosome from their mother.

5. In terms of size, the X chromosome is about three times the size of the Y chromosome and contains about 900 genes, while the Y chromosome has about 55 genes.

6. Female mammals have two X chromosomes in each cell. However, one of the X chromosomes is inactive. This inactivation prevents transcription so that the amount of X-linked genes does not double, which can be potentially dangerous. An inactive X chromosome is compacted in the nucleus as a small compact structure called a cargo body. Objects are usually used to determine gender.

7. Changes in the structure or number of X chromosomes can lead to disease. For example, trisomy X syndrome is caused by having three X chromosomes instead of two X chromosomes. Turner syndrome occurs when women inherit only one copy of the X chromosome.

8. Some women have excellent color vision. This condition is very rare and is called tetrachromacy and is linked to the X chromosome. These women can see up to 100 million shades of color because they have four types of cone cells in their eyes instead of the usual three.

9. Contrary to popular belief, the calico is not a breed of cat, but a distinct coat color pattern that is linked to the X chromosome. More than 95% of calico cats are female. The patches of fur on a calico cat are orange and black, and the color depends on which X chromosome is inactive within each patch of the coat.

10. In genealogy, male descent is often traced using the Y chromosome, as it is only passed down from the father.

11. All people who carry a Y chromosome are related through a common XY ancestor who lived (probably) about 300,000 years ago.

12. The Y chromosome contains a gene called SRY, which causes the testicles to form in the embryo and leads to the development of the internal and external reproductive organs of the male sex. If a mutation occurs in the SRY gene, the embryo will develop female reproductive organs despite having XY chromosomes.

13. Variation in the number of sex chromosomes in a cell is quite normal. Some men have more than two X chromosomes in all their cells (the XXY condition is called Klinefelter syndrome), and many men lose the Y chromosome as they age. Smoking may accelerate this process.

14. Some genes that were thought to be lost on the Y chromosome have actually been moved and transferred to other chromosomes.

15. Most of the Y chromosome consists of repetitive DNA fragments, and special techniques are needed to sequence and determine the order of these very similar fragments.

What are chromosomal abnormalities?

Different types of chromosomal abnormalities can be divided into two main groups: numerical abnormalities and structural abnormalities.

Numerical anomalies

The condition in which a person loses one of his pairs of chromosomes are called monosomy, and the condition in which a person has more than two chromosomes instead of one pair is called trisomy. An example of a disease caused by numerical abnormalities is Down syndrome, which is characterized by mental retardation, learning problems, specific facial features, and weak muscle tone (hypotonia) in infancy. A person with Down syndrome has three copies of chromosome 21 instead of two. For this reason, Down syndrome is also called trisomy 21. An example of monosomy, in which a person lacks one chromosome, is Turner syndrome. In Turner syndrome, the female sex is born with only one sex chromosome, an X, and is usually shorter than usual and is unable to have children, and has other problems.

Structural abnormalities

Chromosome structure can be changed in several ways:

Deletion: A part of the chromosome is lost or deleted.

Duplication: Part of the chromosome is duplicated, resulting in extra genetic material.

Translocation: A part of a chromosome is transferred to another chromosome. There are two main types of chromosomal translocations. In reciprocal translocation, parts of two different chromosomes are exchanged. In Robertson translocation, a complete chromosome is attached to another chromosome at the centromere.

Inversion: A part of the broken chromosome turns upside down and then rejoins. As a result of this phenomenon, the genetic material is reversed.

Rings: A part of the chromosome breaks and forms a ring or circle. This phenomenon can be associated with the loss of genetic material or the genetic material does not change.

Most chromosomal abnormalities occur randomly in the egg or sperm. In these cases, there is an abnormality in every cell of the body. However, some abnormalities occur after fertilization, so some cells are abnormal and others are not.

Chromosomal abnormalities can be inherited from one parent (such as a translocation) or present in a new individual. This is why when it is determined that a child has some kind of abnormality, chromosomal studies are often done on the parents.

How do chromosomal abnormalities occur?

Chromosomal abnormalities usually occur when an error occurs in cell division. There are two types of cell division: mitosis and meiosis.

Mitosis results in two cells that are copies of the original cell. A cell with 46 chromosomes divides and becomes two cells, each of which has 46 chromosomes. This type of cell division occurs throughout the body except for the reproductive organs. This is how most of the cells that make up our body are made and replaced.

Meiosis leads to the production of cells that have half the number of chromosomes, i.e. 23 chromosomes, instead of 46 chromosomes. Meiosis occurs in the reproductive organs and leads to the formation of eggs and sperm.

In both processes, the correct number of chromosomes is supposed to be established in the resulting cells. Of course, errors in cell division can lead to the formation of cells that have fewer or more copies of chromosomes. Errors can also occur when chromosomes are duplicated.

Other factors that can increase the risk of chromosomal abnormalities are:

Maternal age: Women are born with all the eggs they will have in their lifetime. Some researchers believe that with age, errors appear in the egg’s genetic material. Older women are at higher risk of giving birth to babies with chromosomal abnormalities than younger women. Because men produce new sperm throughout their lives, paternal age does not increase the risk of chromosomal abnormalities.

Environment: Although there is no conclusive evidence that certain environmental factors cause chromosomal abnormalities, the environment may play a role in the occurrence of genetic errors.


How to rejuvenate an aging immune system?




immune system
Scientists succeeded in rejuvenating the immune system of old mice with a new therapeutic approach.

How to rejuvenate an aging immune system?

After scientists reduced abnormal stem cells in old animals, mice’s immune systems became more youthful. This technique enhanced the response of old rodents to viral infection and reduced signs of inflammation. In this method, published March 27 in the journal Nature, old mice are treated with an antibody to reduce a population of stem cells that give rise to other types of cells, such as those involved in inflammation.

Excessive inflammation can wreak havoc on the body, and pro-inflammatory stem cells proliferate during aging in mice and humans.

Imbalanced immune system

For decades, researchers in Irving Weissman’s group at Stanford University in California have closely followed the fate of blood stem cells. These cells replenish the supply of red blood cells (which carry oxygen from the lungs to all parts of the body) and white blood cells (which are key components of the immune system).

Balancing the blood stem cell population can rejuvenate the immune system

In 2005, Weissman and colleagues found that as mice age, their blood stem cell population changes. In young mice, there is a balance between two types of blood stem cells, each contributing to a different branch of the immune system. The adaptive compartment produces antibodies and T cells that target specific pathogens. The innate part produces general responses such as inflammation against infection.

However, in old mice, the balance between the two parts of the immune system is skewed towards the production of more pro-inflammatory innate immune cells. Similar changes have been reported in the blood stem cells of aging humans, and researchers speculate that this could lead to a reduced ability to produce new antibodies and T-cell responses. This may explain why the elderly are more susceptible to serious infections from pathogens such as influenza viruses and SARS-CoV-2, and why their response to vaccination is weaker than that of younger people.

Restore the balance of the immune system

If the researchers’ conclusions are correct, restoring balance to the blood stem cell population could also rejuvenate the immune system.

The researchers tested this hypothesis by producing antibodies that bind to blood stem cells, which mainly produce innate immune cells. They then injected these antibodies into old mice with the hope that their immune systems would destroy the stem cells attached to the antibodies.

Antibody treatment rejuvenated the immune system of treated mice. They showed a stronger reaction to the vaccination than the old mice that did not receive the treatment and were better at warding off the viral infection. The treated mice also had lower levels of proteins associated with inflammation, which the authors say shows how different populations of blood stem cells affect the aging of the immune system.

It is possible that the effect of antibody treatment is more than affecting the blood stem cell population. Antibody therapy may also affect the environment in which blood stem cells can live. On the other hand, the said treatment can clear other old cells from the body or stimulate immune responses, thus affecting how mice respond to vaccines and viruses.

It will be years before Weissman and his colleagues’ approach can be tested in humans, but many aspects of the stem cell biology that underlies the production of immune cells are similar in mice and humans.

Weissman’s team is working on a similar approach to rebalance the blood stem cells of elderly people. He believes that even if there is sufficient funding and no unexpected obstacles arise, it will take at least three to five years before they can test their method on humans. In the meantime, the researchers will continue to study the mice to learn more about other effects of the antibody therapy, such as whether it affects the rate of cancer or inflammatory diseases. “The blood-forming system of young and old blood is very different,” says Weissman. “The difference is not just in the bone marrow, but throughout the body.”

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How can hacking the immune system help slow aging?




immune system
Our immune system weakens over time and this could explain the negative effects of aging. Manipulation of the immune system may alter the aging process.

How can hacking the immune system help slow aging?

Stem cell researcher Carolina Florian couldn’t believe what she was seeing. His old laboratory mice began to look younger. They were more lively and their fur was shinier. However, all he had done was a short treatment a few weeks earlier with a drug that modified the organization of proteins in a type of stem cell.

Stem cell researcher Carolina Florian couldn’t believe what she was seeing. His old laboratory mice began to look younger. They were more lively and their fur was shinier. However, all he had done was a short treatment a few weeks earlier with a drug that modified the organization of proteins in a type of stem cell.

When technicians repeating Florian’s experiment in two other laboratories reached the same conclusion, Florian became more confident that the treatment in question would rejuvenate the animals. In two papers in 2020 and 2022, his team explained how this process extended the lifespan of mice and kept them in good physical condition into old age.

The purpose of Florian Elixir is the immune system. The immune cells he targeted are called hematopoietic stem cells, which give rise to mature immune cells. By circulating the blood, a mixture of these cells enters all the organs and affects all the functions of the body. However the molecular composition of hematopoietic stem cells changes during aging, and this upsets the balance of the immune cells that these stem cells produce.

Florian, who works at the Bleuge Biomedical Research Institute in Barcelona, ​​says reversing the misalignment that occurs over time appears to reverse many of the problems of aging, not only in the immune system but in the rest of the body as well.

Health and agingDescription Researchers think the immune system could be the key to healthy aging.

In a paper published in March in the journal Nature, researchers show that restoring the balance between two key types of immune cells rejuvenates the immune system of aging mice and improves the animals’ ability to respond to vaccines and ward off viral infections.

Other scientists have used different experimental methods to reach a similar conclusion: Rejuvenating the immune system rejuvenates many organs in animals, at least in mice. More interestingly, evidence shows that aging of the immune system may cause aging of those organs.

The potential of the findings to help people stay healthy in old age is tantalizing. But applying this knowledge and using it in clinics will be challenging. Tampering with the immune system can be dangerous. Therefore, researchers initially aimed at low-risk goals such as improving the response of the elderly to vaccination and improving the efficacy of cancer immunotherapy.

Vittorio Sebastiano, a stem cell scientist at the Stanford School of Medicine in California, says the prospect that reversing aging might curb age-related diseases is enticing, but we proceed with caution.

Weakened immunity

The human immune system is a complex system whose many cellular and molecular components work together to help a person grow, protect him from infection, help heal wounds, and destroy cells that are becoming cancerous. But along with aging and changing the composition of the system, its efficiency decreases. In old age, people become susceptible to a wide range of infectious and non-infectious diseases and become more resistant to the protective power of vaccines.

Aging of the immune system may cause aging of different body parts

The immune system has two main components: the innate system, which indiscriminately destroys invading pathogens, and the more precise adaptive immune system, whose components learn to recognize and produce antibodies against specific foreign bacteria and viruses.

Hematopoietic stem cells in the bone marrow produce both arms of the immune system. They differentiate into two main types (lymphoid cells and myeloid cells), which then undergo further differentiation.

Lymphoid cells are primarily responsible for adaptive immunity and include B cells that produce antibodies, T cells that help attack invaders and coordinate immune responses and natural killer cells that kill infectious cells. Myeloid cells comprise a group of cell types that are mainly involved in innate immunity.

protein inside cellsProteins in stem cells that produce immune cells become more symmetrical as they age (right).

One of the first changes in the immune system during aging is the shrinking of the thymus, which begins after puberty. The thymus is where T cells mature, but much of this tissue turns to fat by the third decade of life, reducing the production of new T cells and weakening the immune system.

In addition, the function of T cells changes with age and they are not as specialized in detecting infectious agents as before. The ratio of different types of immune cells in the circulation also changes. The ratio of myeloid to lymphoid cells is significantly skewed toward myeloid cells and this can cause inflammation. In addition, an increasing number of immune cells become senescent, meaning that they stop replicating but do not die.

Aging cells usually occur when they undergo mutations. When cells are in this condition, they begin to release inflammatory signals and mark themselves for destruction.

An important anti-cancer and wound-healing mechanism works best when young. But when too much damage accumulates with age and the immune cells themselves age, this mechanism is disrupted. Senescent immune cells, attracted by inflammatory signals from senescent tissues, secrete their own inflammatory molecules. Therefore, they are not cleared properly but instead, add to the inflammation that also damages the surrounding healthy tissues. This phenomenon is known as inflammatory aging. This turns into a terrible positive feedback loop, says Aran Akbar, an immunologist at University College London. Evidence shows that this feedback loop is initiated by the immune system.

Laura Niedernhofer from the University of Minnesota in Minneapolis has shown in a series of experiments in mice that the aging of immune cells causes the aging of other tissues. He says these cells are very dangerous.

His team used genetic methods to delete an important DNA repair enzyme in the immune system of mice. The animals remained healthy until adulthood, but after that, they were no longer able to correct the accumulated mutations, and different types of immune cells began to age.

A few months later, an increasing number of cells in organs such as the liver and kidney were also senescent, and signs of organ damage appeared. When the scientists gave old mice immune cells from the spleens of young, healthy mice, all of these effects were reversed. All of this suggests that modifying the aging properties of the immune system could help prevent or reduce age-related diseases, Niederenhofer says.

Fight against aging

Many scientists are trying to do this from very different angles. Many approaches suggest that very short treatment of the immune system may have long-term effects and minimize side effects.

One of the ways to deal with aging immune cells is to use drugs to remove or inhibit the inflammatory factors that these cells release. Aging immune cells in humans can be changed, Niederenhofer says. If you smoke, they increase and if you exercise, they decrease.

Modifying the immune system can help prevent or reduce aging-related diseases

Some drugs, such as dasatinib, which is approved for the treatment of certain cancers, and quercetin, which is marketed as an antioxidant dietary supplement but not approved as a drug, slow cellular aging, and several trials are testing their effects on aging-related diseases.

Niederneuhofer is conducting a small clinical trial in elderly people with sepsis. Sepsis is a condition that becomes more deadly with age. His team is also conducting experiments to assess which types of immune cells are most involved in aging in the body, and their results could help design more precise treatments. Two types of cells (T cells and natural killer cells) are emerging as the main contenders, he says. He plans to examine natural products and approved drugs for their ability to interact with these types of immune cells during aging.

Akbar thinks targeting inflammation may be just as effective as targeting senescent cells. He and his colleagues conducted a study in healthy volunteers using the investigational compound lozepimod, which inhibits an enzyme involved in the production of a type of inflammatory molecule called cytokines. They treated volunteers with this drug for four days and then measured their skin’s response to an injection of the chickenpox virus over the course of a week. Most people are exposed to this virus during their life and this virus often stays in the body.

As people age, they lose their immunity to the chicken pox virus, and this time it can appear as shingles. The drug restored the immune response in the skin of older volunteers to a level similar to that of young volunteers. Akbar has found in unpublished studies that the same strong results persist up to three months later. Temporarily inhibiting inflammation in this way to keep the immune system functioning may similarly enhance the response of older patients to flu vaccinations, he says.

Boosting the immune system

The value of priming the elderly immune system prior to vaccination has been demonstrated in a series of clinical trials led by Joanne Mannick, CEO of Boston, Massachusetts-based Tornado Therapeutics. The trials tested analogs of the drug rapamycin and other drugs with similar mechanisms that target the immune system and are approved to prevent organ transplant rejection and to treat certain cancers.

The mentioned drugs inhibit an enzyme called mTOR, which is vital for many physiological functions and whose function is impaired in aging. Participants were treated with doses of the drug that were low enough to avoid side effects for several weeks before receiving the flu vaccine. This treatment regimen improved their response to the vaccine and increased their immune system’s ability to resist viral infections.

vaccinationVaccines are less effective in older people, but new approaches could increase their potency.

However the drug rapamycin can increase susceptibility to infection and affect metabolism, so Manick is planning trials with similar drugs that could be safer. “There are different ways to improve the immune system,” he notes.

Another way is to try to restore thymus function to maintain the production of new T cells. Jarrod Dudakoff, an immunologist at the Fred Hutchinson Cancer Center in Seattle, is studying the basic biology of thymus cells to understand how they regenerate after bouts of stress. Dudakov says it’s a little early to see how our understanding of this can be applied in the clinic. But he thinks it’s important to preserve the ability of the thymus to produce T cells.

Others try to fight aging by producing thymus tissue from powerful stem cells and then transplanting it. But Greg Fahey, chief scientific officer at Intervene Immune in Torrance, Calif., says there’s no need to wait to achieve those long-term prospects because synthetic growth hormone regenerates thymus tissue. He is conducting small studies in healthy volunteers using growth hormones as part of a mixture of compounds.

Preliminary results show that the amount of functional thymus tissue in the participants increased and their epigenetic clock (a biomarker of aging) was reversed by several years. Fahey is conducting further testing to see if the drug combination also improves the physical condition of the participants.

Turn back the clock

Another approach that has yet to reach the clinic is reprogramming immune cells to try to turn back the clock on cells that have aged. This procedure involves temporarily placing the cells in a dish exposed to a combination of transcription factors that induce a pluripotent state in mature cells.

Sebastiano and colleagues have shown in human cells that this corrects the epigenetic changes that accompany aging. He has founded a startup to use this technique to tackle a type of cancer treatment called CAR T, in which T cells are engineered outside the body to target and destroy a person’s cancer. However, the T cells may age before they are returned to the person. Rejuvenating them makes production faster and more powerful, says Sebastiano.

One of the challenges of aging studies is the inability to measure aging accurately

Florian’s approach also aims to produce healthier immune cells within the body. Hematopoietic stem cells in the blood develop epigenetic changes and their environment also changes with age. This causes the proteins to arrange themselves in a more symmetrical way in the cells (a process known as polarization), which shifts the balance of differentiation of stem cells towards myeloid cells.

In his studies, Florian used a four-day treatment with a compound called CASIN, which inhibited part of this process to correct polarization and help the mice live longer. When hematopoietic stem cells from aged mice that had received CASIN were transplanted into aged mice that had not received the treatment, the same life-extending effects were seen. Florian hopes to turn his results into a practical method in the clinic. He thinks his drug may help rebuild the immune system after receiving cancer chemotherapy.

The challenge of measuring aging

Research on immune aging faces major challenges. One of the challenges in aging studies of all organs is the inability to measure aging accurately. “We don’t know in a quantitative, measurable, predictable way what aging means at the molecular level in different cell types,” says Sebastiano. “Without these metrics, it is very difficult to demonstrate rejuvenation.”

Another challenge is the difficulty in determining the characteristics that make an immune cell unique. Until recently, it was difficult to show where each of the immune cell subsets lived and how they changed over time. But technologies such as single-cell RNA sequencing, which quantitatively measures genes expressed in single cells, have made the analysis more challenging. For example, a large study of immune cells in the blood of humans and mice across a range of ages, published last November, revealed 55 subpopulations. Only 12 subpopulations of cells changed with age.

By collaborating with different research areas, scientists hope to prove that the immune system plays an important role in healthy aging. Don’t expect an elixir of youth anytime soon, says Florian. Aging research will take a long time, but it can help design tools that will be transformative.

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Discovery of the brain circuit that manages inflammation




brain circuit

Researchers believe that using this new brain circuit could lead to new treatments for many immune disorders.

Discovery of the brain super circuit that manages inflammation

Researchers have found that brainstem neurons act as regulators of inflammation. These neurons can increase or decrease inflammation in response to signals sent by the vagus nerve, a collection of thousands of nerve fibers that connect the brain and internal organs.

A new study in mice shows that a peripheral immune stimulus powerfully activates the body-brain axis to regulate immune responses, according to AI. Pro- and anti-inflammatory cytokines communicate with specific populations of vagal neurons to inform the brain of an emerging inflammatory response. The brain, in turn, strongly modulates this environmental immune response process.

Cytokines are a group of water-soluble protein molecules that are secreted from various cells in response to a stimulus and are responsible for transmitting messages between cells. The consequence of the presence of cytokines is a change in the behavior of cells with secreted cytokine receptors, including growth, change, or cell death. The action and effect of cytokine produced by one cell includes more cells around the same cell, but it can have a systemic action and effect on the whole organism.

Cytokine has the effect of changing the secreting cell itself and changes in other cells, and like a hormone, it can have effects on cells far away from it.

The vagus nerve is also the longest brain nerve and the tenth pair of brain nerves out of 12 pairs of brain nerves, which is involved in swallowing food, speaking, parasympathetic activities, and digestion. The motor part of this nerve is somatic and innervates the larynx, soft palate, and pharynx. This nerve is the longest cranial nerve, and like most cranial nerves, it starts from the brain stem and is divided into many branches that innervate most of the muscles of the pharynx and larynx, esophagus, stomach, and parasympathetic heart, lung, liver, spleen, etc.

Discovery of the neuro-immune axis

Based on this study, the researchers used single-cell RNA sequencing, combined with functional imaging, to identify circuit components of this neuro-immune axis and show that its selective manipulation can effectively suppress the pro-inflammatory response while maintaining an anti-inflammatory state. 

This new brain circuit, like a thermostat, helps increase or decrease inflammatory responses so the body responds in a healthy way, said Dr. Hao Jin, who began the study as a postdoctoral researcher in Dr. Zucker’s lab.

Looking at past research, it makes sense that a master regulator controls this critical response, the researchers say. Many psychosomatic effects can actually be related to brain circuits that tell your body something.

They believe that using this new brain circuit could lead to new treatments for many immune disorders.

Promising therapeutic potential

Brain-induced transformation of an immune response pathway offers new possibilities in modulating a wide range of immune disorders, from autoimmune diseases to cytokine shock.

“This new discovery could open up an exciting therapeutic area for controlling inflammation and immunity,” said Charles Zucker, senior author of the study.

Researchers believe that controlling this newly discovered brain circuit could lead to new treatments for common autoimmune diseases including rheumatoid arthritis, type 1 diabetes, multiple sclerosis, lupus, and inflammatory bowel disease.

Read more: Brain cancer vaccine success in human trials

This new control agent could also help treat other diseases such as prolonged COVID-19 syndrome, organ transplant rejection, and cytokine storms caused by COVID-19. According to the researchers, inhibiting the activity of this circuit could make a difference in a wide range of conditions that affect the immune system and help treat dysregulated inflammatory states in people suffering from diseases and immune disorders. This study was published in the journal Nature.

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