Muscle fibroblasts and stem cells stimulate motor neurons in an age and exercise-dependent manner.

IF 8 1区 医学 Q1 CELL BIOLOGY Aging Cell Pub Date : 2024-11-18 DOI:10.1111/acel.14413
Casper Soendenbroe, Peter Schjerling, Cecilie J L Bechshøft, Rene B Svensson, Laurent Schaeffer, Michael Kjaer, Bénédicte Chazaud, Arnaud Jacquier, Abigail L Mackey
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Abstract

Exercise preserves neuromuscular function in aging through unknown mechanisms. Skeletal muscle fibroblasts (FIB) and stem cells (MuSC) are abundant in skeletal muscle and reside close to neuromuscular junctions, but their relative roles in motor neuron maintenance remain undescribed. Using direct cocultures of embryonic rat motor neurons with either human MuSC or FIB, RNA sequencing revealed profound differential regulation of the motor neuron transcriptome, with FIB generally favoring neuron growth and cell migration and MuSC favoring production of ribosomes and translational machinery. Conditioned medium from FIB was superior to MuSC in preserving motor neurons and increasing their maturity. Lastly, we established the importance of donor age and exercise status and found an age-related distortion of motor neuron and muscle cell interaction that was fully mitigated by lifelong physical activity. In conclusion, we show that human muscle FIB and MuSC synergistically stimulate the growth and viability of motor neurons, which is further amplified by regular exercise.

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肌肉成纤维细胞和干细胞刺激运动神经元的方式与年龄和运动有关。
运动通过未知的机制在衰老过程中保护神经肌肉功能。骨骼肌成纤维细胞(FIB)和干细胞(MuSC)在骨骼肌中含量丰富,并靠近神经肌肉接头,但它们在运动神经元维持中的相对作用仍未被描述。利用胚胎大鼠运动神经元与人MuSC或FIB的直接共培养,RNA测序揭示了运动神经元转录组的深刻差异调控,FIB通常有利于神经元生长和细胞迁移,而MuSC则有利于核糖体和翻译机制的产生。在保存运动神经元和提高其成熟度方面,FIB的条件培养基优于MuSC。最后,我们确定了供体年龄和运动状态的重要性,并发现运动神经元和肌肉细胞相互作用的扭曲与年龄有关,而终身体育锻炼可完全缓解这种扭曲。总之,我们的研究表明,人类肌肉 FIB 和 MuSC 能协同刺激运动神经元的生长和存活,而定期运动能进一步增强这种作用。
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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
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