SCIENCE

How Cells Choose Their Path: The Role of Linker Histones in Blood Cell Development

Tue Oct 21 2025

Recent research sheds light on how certain molecules, called linker histones, guide blood cells to become either immune fighters (lymphoid) or helpers (myeloid).

As we age, our blood cells tend to favor becoming helpers

This is because the instructions in their DNA become harder to read. Linker histones act like librarians, organizing and compacting the DNA. When there are more linker histones, the DNA becomes more ordered, and the cells are more likely to become immune fighters.

The study found that when linker histones are increased, certain genes that push cells to become helpers are harder to access

One key gene, Hlf, is tucked away in a tightly packed region of DNA. If this gene isn't turned off, the cells can't become immune fighters.

Interestingly, the body has a way to reduce linker histones using enzymes called aspartyl proteases

These enzymes are activated by a messenger called interferon alpha. If these enzymes are blocked, linker histones stay high, and cells are more likely to become immune fighters.

This research is crucial because it helps us understand why blood cells might not work properly as we age. It also opens up new possibilities for treatments that could help balance blood cell development.

questions

    What other factors, besides linker histones and aspartyl proteases, could be contributing to the myeloid bias observed in aging or exhausted HSPCs?
    If linker histones are the 'packing peanuts' of the genome, what happens when they get squished too tightly?
    Is the observed myeloid bias in aging HSPCs a natural phenomenon, or is it influenced by external factors such as environmental toxins or dietary components?

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