Aged hematopoietic stem cells are refractory to bloodborne systemic rejuvenation interventions

Theodore Ho(University of California, San Francisco), Paul V. Dellorusso(Columbia University), Evgenia Verovskaya(University of California, San Francisco), Sietske T. Bakker(University of California, San Francisco), Johanna Flach(University of California, San Francisco), Lucas K. Smith(University of California, San Francisco), Patrick Ventura(University of California, San Francisco), Olivia Lansinger(University of California, San Francisco), Aurélie Hérault(University of California, San Francisco), Si Yi Zhang(University of California, San Francisco), Yoon-A Kang(University of California, San Francisco), Carl A. Mitchell(Columbia University), Saul Villeda(University of California, San Francisco), Emmanuelle Passegué(University of California, San Francisco)
The Journal of Experimental Medicine
April 16, 2021
Cited by 98Open Access
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Abstract

While young blood can restore many aged tissues, its effects on the aged blood system itself and old hematopoietic stem cells (HSCs) have not been determined. Here, we used transplantation, parabiosis, plasma transfer, exercise, calorie restriction, and aging mutant mice to understand the effects of age-regulated systemic factors on HSCs and their bone marrow (BM) niche. We found that neither exposure to young blood, nor long-term residence in young niches after parabiont separation, nor direct heterochronic transplantation had any observable rejuvenating effects on old HSCs. Likewise, exercise and calorie restriction did not improve old HSC function, nor old BM niches. Conversely, young HSCs were not affected by systemic pro-aging conditions, and HSC function was not impacted by mutations influencing organismal aging in established long-lived or progeroid genetic models. Therefore, the blood system that carries factors with either rejuvenating or pro-aging properties for many other tissues is itself refractory to those factors.


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