Biological processes linked to aging are vital for the regeneration of heart tissue, study finds
Researchers found that an
“aging” mechanism known as senescence is activated for a short period of
time following injury to the heart muscle of mice as a vital part of
the heart’s healing process.
By JUDY SIEGEL-ITZKOVICH, Jerusalem Post, JUNE 16, 2024
Monitor your symptoms carefully if you're at risk of a heart attack (photo credit: INGIMAGE)
Aging of bodily tissues typically causes them to break down and eventually fail. However, researchers at the Weizmann Institute of Science in Rehovot
have discovered that biological processes that are usually linked to
aging are, in fact, vital for the regeneration of heart tissue.
This surprising conclusion emerges from a study just published in the prestigious journal Nature Cardiovascular Research.
The study was conducted by a research team led by Dr. Rachel Sarig and
research student Lingling Zhang from Prof. Eldad Tzahor's laboratory,
which is one of the leading labs in the world in cardiac healing and
regeneration research.
The scientists have revealed in unprecedented detail – at the level
of individual cells – how an “aging” mechanism known as senescence is
activated for a short period of time following injury to the heart
muscle of mice as a vital part of the heart’s healing process. This is
the latest in a series of studies revealing the crucial roles that
senescence plays in the development and regeneration of tissues.
“Despite a growing number of studies showing the positive aspects of
senescence, the common view in the field remains that senescence is
deleterious for human health. We hope that our study serves to change
that view,” they wrote.
The Weizmann Institute is set to open a medical school in October of 2025. (credit: WEIZMANN INSTITUTE OF SCIENCE)
Findings raise 'red flag'
The findings raise a red flag
regarding the currently investigated therapeutic approach to eliminating
senescent cells—a practice that might prove dangerous.
The team described the regenerative senescence signature of the injured mouse heart through proteomics and single-cell RNA sequencing
(scRNA-seq). They concluded that “aged cells are required for neonatal
mouse heart regeneration and for Agrin-mediated cardiac repair in adult
animals and provide insights into the essential role of Egr1 in
senescence and regeneration.”
“Numerous studies across different organs and disease models,
including aging and models of heart diseases, have explored the prospect
of eliminating senescent cells in order to enhance tissue function,”
they wrote. “Our study, alongside previous research demonstrating
essential beneficial roles for senescent cells, underscores the need for
caution when trying to non-specifically remove these cells using
various drugs, as such interventions could be harmful if applied during
the healing process.”
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