Gut microbiota transplantation from young adult mice fails to restore low bone and muscle mass in old mice.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Lina Lawenius, Daniel Hägg, Karin Horkeby, Karin H Nilsson, Jianyao Wu, Louise Grahnemo, Claes Ohlsson, Klara Sjögren
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Abstract

Aging is associated with reduced lean and bone mass, as well as alterations in gut microbiota composition. We previously demonstrated that gut microbiota composition differs between young adult and old mice, and that transplanting gut microbiota from old donors into young germ-free mice reduces lean mass, but not bone mass, compared with transplantation from young adult donors. In this study, we investigated whether the reduced lean and bone mass observed in old mice could be restored through gut microbiota transplantation from young adult donors. Old mice (18-mo old) were treated with antibiotics to deplete their gut microbiota and subsequently transplanted with gut microbiota from either young adult (5-mo old) or old (21-mo old) donors. Recipient mice colonized with gut microbiota from young adult donors showed distinct beta and alpha diversity compared with those colonized with gut microbiota from old donors, demonstrating successful transplantation. However, no differences in lean or bone mass were observed between old mice transplanted with gut microbiota from young adult donors and those receiving gut microbiota from old donors. In conclusion, our findings demonstrate that gut microbiota composition differs in mice transplanted with young adult compared with old gut microbiota but neither reduced lean mass nor reduced bone mass in old mice can be restored through gut microbiota transplantation from young adult donors.NEW & NOTEWORTHY Aging is associated with reduced lean and bone mass and changes in gut microbiota (GM). We tested whether transplanting young adult GM could reverse these age-related conditions in old mice. GM transplantation resulted in distinct GM compositions between mice receiving young adult versus old donor GM, but neither lean nor bone mass was restored in old mice. These findings suggest that GM from young adult mice cannot restore musculoskeletal deficits in aging.

年轻成年小鼠的肠道菌群移植不能恢复老年小鼠的低骨和肌肉质量。
衰老与瘦骨量和骨量减少以及肠道菌群组成的改变有关。我们之前证明了年轻成年小鼠和老年小鼠的肠道菌群组成不同,并且与年轻成年小鼠的移植相比,将老年供体的肠道菌群移植到年轻无菌小鼠中会减少瘦体重,但不会减少骨量。在这项研究中,我们研究了是否可以通过年轻成年供体的肠道菌群移植来恢复老年小鼠瘦骨量和骨量的减少。老龄小鼠(18个月大)接受抗生素治疗以消耗其肠道微生物群,随后移植来自年轻成年小鼠(5个月大)或老年小鼠(21个月大)供体的肠道微生物群。移植了年轻成年供体肠道菌群的受体小鼠与移植了老年供体肠道菌群的受体小鼠相比,显示出明显的β和α多样性,表明移植成功。然而,在移植了年轻成年供体肠道菌群的老年小鼠和接受老年供体肠道菌群的老年小鼠之间,没有观察到瘦骨量或骨量的差异。总之,我们的研究结果表明,与年老的肠道菌群相比,年轻的成体移植小鼠的肠道菌群组成不同,但通过年轻的成体供体的肠道菌群移植,年老小鼠的瘦体重和骨量的减少都无法恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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