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bioRxivCell BiologyPreprint

Human hypothalamic neural stem cells transplantation ameliorates age-associated dysfunction through SNS/eNAMPT axis activation in aged mice

Yanuar Alan SulistioiD, Yuna Lee, Kelvin PieknelliD, Sebin Hong, Jumi KimiD, Min Jong Seok, Na-Kyung Lee, Kyu‐Sang ParkiD, Taeui Hong, Suyeon Choi, Ki Woo KimiD, Dong Joo YangiD, Woong‐Yang ParkiD, Kyung Yeon HaniD, Seul Gi Yoon, Il Yong Kim, Je Kyung SeongiD, Tae Yong LeeiD, Min-Sung Kim, Sang‐Hun LeeiD

PDFDOI

Abstract

The hypothalamus is the brain region that regulates systemic body metabolism and multiple brain functions. The adult hypothalamus harbors neural stem/precursor cell (NSC)-like cells. Along with age-related body changes, the hypothalamic NSC (htNSC) population declines, indicating the potential of htNSC replacement as an anti-aging strategy. Here, we developed protocol to generate htNSCs from human pluripotent stem cells (hPSCs). Implanting the hPSC-derived htNSCs into the hypothalamus of aged mice ameliorated age-related declines in metabolic fitness, physical capacity, and cognitive function. Mechanistically, these anti-aging effects were mediated by inter-tissue communication: enhanced neuronal activity in the htNSC-transplanted hypothalamus stimulated adipose tissues to produce and release the anti-aging molecule eNAMPT into systemic circulation via the sympathetic nervous system. Concurrently, the aged inflammatory environment in the hypothalamus was alleviated by peripheral anti-aging signals. Collectively, our findings support the potential of anti- or healthy aging therapies by targeting hypothalamus.

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