# Mitochondrial Maintenance Mechanisms of Stem Cells and Aging

> **NIH NIH R01** · COLUMBIA UNIVERSITY HEALTH SCIENCES · 2021 · $388,723

## Abstract

Summary:
Understanding the mechanisms driving aging may lead to innovative strategies to increase health span, an
effort that would carry enormous human and economic benefit. The fact that many species (typically, though
not exclusively, more slowly developing, longer-lived and larger species) possess somatic stem cells capable
of self-renewal and tissue regeneration calls into question why these organisms and their somatic stem cells
do age whereas the germline apparently does not. The function of somatic stem cells declines with age, and
this decline is at least in part explained by cell-intrinsic mechanisms. While often viewed as a degenerative
condition, aging of somatic stem cells may in fact be a reflection of the pervasive action of protective stem cell
maintenance mechanisms that confer differential susceptibility to stress and injury compared to mature cells.
The `immortal' germline, however, undergoes extreme selection so that only the fittest gametes transmit their
genome to the next generation. Evidence suggests that the quality of mitochondrial function is one mechanism
based on which gametes are selected. In contrast to gametes somatic stem cells rely predominantly on
glycolytic ATP production, while most mature cells use mitochondrial respiration. Likely because of their
reliance on glycolysis, evidence suggests that hematopoietic stem cells, the best characterized adult stem cell
type, are less susceptible to impaired mitochondrial function than progenitors. We therefore hypothesize that
mitochondria play an important role in HSC maintenance that is not directly dependent on ATP production. We
indeed observed that HSCs have high mitochondrial mass and do not perform mitophagy. Furthermore,
impairment of mitochondrial dynamics decreases the number of HSCs with extensive lymphoid potential and
induced cycling of the entire HSC compartment. These data show that mitochondria do play specific roles in
HSC maintenance. In this proposal, we examine the mechanisms underlying mitochondrial maintenance of
HSCs, and its implication for the aging of HSCs. We will test the hypothesis that impairment of mitochondrial
maintenance of HSCs will negatively affect HSC function in young mice, but may lead to longer maintenance of
HSC function in aged mice. Somatic stem cell maintenance as a mechanism underlying organismal aging
would be remarkably consistent with an evolutionary theory of aging, the antagonistic pleiotropy theory, which
proposes that mechanisms that provide reproductive or survival benefit early in life are detrimental late in life
and contribute to aging.

## Key facts

- **NIH application ID:** 10192621
- **Project number:** 5R01AG055910-05
- **Recipient organization:** COLUMBIA UNIVERSITY HEALTH SCIENCES
- **Principal Investigator:** HANS-WILLEM E SNOECK
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $388,723
- **Award type:** 5
- **Project period:** 2017-07-01 → 2022-05-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10192621

## Citation

> US National Institutes of Health, RePORTER application 10192621, Mitochondrial Maintenance Mechanisms of Stem Cells and Aging (5R01AG055910-05). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/10192621. Licensed CC0.

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