{"id":29605,"date":"2024-08-06T15:50:37","date_gmt":"2024-08-06T19:50:37","guid":{"rendered":"https:\/\/biology.mit.edu\/?p=29605"},"modified":"2024-08-06T15:52:50","modified_gmt":"2024-08-06T19:52:50","slug":"in-immune-cells-x-marks-the-spots","status":"publish","type":"post","link":"https:\/\/biology.mit.edu\/in-immune-cells-x-marks-the-spots\/","title":{"rendered":"In immune cells, X marks the spot(s)"},"content":{"rendered":"
There are many known sex differences in health and disease: cases in which either men or women are more likely to get a disease, experience a symptom, or have a certain drug side effect. Some of these sex differences are caused by social and environmental factors: for example, when men smoked more than women, men were more likely to develop lung cancer. However, some have biological underpinnings. For example, men are more likely to be red-green colorblind because the relevant gene is on the X chromosome, of which men with XY chromosomes have no backup copy for a dysfunctional version.<\/p>\n
Often, the specific factors contributing to a sex difference are hard to tease apart; there may not be a simple way to tell what is caused by sex chromosomes versus sex hormones versus environment. To address this question, researchers in Whitehead Institute Member David Page\u2019s lab previously developed an approach to identify the contributions of the sex chromosomes to sex differences. Now, Page and former postdoc in his lab Laura Blanton have built on that work by measuring the effects of the sex chromosomes on two types of immune cells. The work,\u00a0published in the journal\u00a0Cell Genomics<\/em>\u00a0<\/a>on August 6, shows that sex chromosome gene expression is consistent across cell types, but that its effects are cell type specific.<\/p>\n Sex differences are common in the function and dysfunction of our immune system. Examples include the typically weaker male immune response to pathogens and vaccines, and the female-biased frequency of autoimmune diseases. Page and Blanton\u2019s work in immune cells examines several genes that have been implicated in such sex differences.<\/p>\n The approach that the researchers used is based on several facts about sex chromosomes. Firstly, although females typically have two X chromosomes and males typically have one X and one Y, there are people with rare combinations of sex chromosomes, who have anywhere from 1-5 X chromosomes and 0-4 Y chromosomes. Secondly, there are two types of X chromosome: The active X chromosome (Xa) and the inactive X chromosome (Xi). They are genetically identical, but many of the genes on Xi are either switched off or have their expression level dialed way down.<\/p>\n Xa does not really function as a sex chromosome since everyone in the world has exactly one Xa regardless of their sex. In people with more than one X chromosome, any additional X chromosomes are always Xi. Furthermore, Page and Blanton\u2019s research demonstrates that Xa responds to gene expression by Xi and Y\u2014the sex chromosomes\u2014in the same manner as do the other 22 pairs of non-sex chromosomes\u2014the autosomes.<\/p>\n With these facts in mind, the researchers collected cells from donors with different combinations of sex chromosomes. Then they measured the expression of every gene in these cells, across the donor population, and observed how the expression of each gene changed with the addition of each Xi or Y chromosome.<\/p>\n This approach was first shared in a\u00a0<\/a>Cell Genomics<\/em><\/a>\u00a0paper<\/a>\u00a0by Page and former postdoc Adrianna San Roman in 2023. They had cultured two types of cells, fibroblasts and lymphoblastoid cell lines, from donor tissue samples. They found that the effects of Xi and Y were modular\u2014each additional chromosome changed gene expression by about the same amount. This approach allowed the researchers to identify which genes are sensitive to regulation by the sex chromosomes, and to measure the strength of the effect for each responsive gene.<\/p>\nDeveloping a method to measure sex chromosome influence<\/h2>\n