Wang Liping, Liang Aihua, Huang Jukai
Key Laboratory of Beijing for Identification and Safety Evaluation of Chinese Medicine, Institute of Chinese Materia Medica, China Academy of Chinese Medical, Beijing, China.
Department of Endocrinology, Beijing University of Chinese Medicine, Dongzhimen Hospital, Beijing, China.
Front Microbiol. 2024 Aug 30;15:1399632. doi: 10.3389/fmicb.2024.1399632. eCollection 2024.
Diabetic nephropathy (DN) presents a significant therapeutic challenge, compounded by complex pathophysiological mechanisms. Recent studies suggest Exendin-4 (Ex-4) as a potential ameliorative agent for DN, albeit with unclear mechanisms. This research investigates the effects and underlying mechanisms of Ex-4-enriched exosomes derived from human umbilical cord mesenchymal stem cells (hUCMSCs) on DN, focusing on their renoprotective properties and interactions with gut microbiota.
Exosomes from hUCMSCs (hUCMSCs-Exo) were loaded with Ex-4 via electroporation. A streptozotocin (STZ) -induced DN mouse model was employed to assess the therapeutic impact of these engineered exosomes. The study further explored immune cell dynamics, mainly CD4 regulatory T (Treg) cells, using bioinformatics, flow cytometry, and the influence of gut microbiota through antibiotic treatment and specific bacterial reintroduction.
Treatment with hUCMSCs-Exo@Ex-4 significantly improved key DN markers, including blood glucose and proteinuria, alleviating kidney damage. A notable decrease in natural Treg cell infiltration in DN was observed, while Ex-4-loaded exosomes promoted CD4 Treg cell induction. The therapeutic benefits of hUCMSCs-Exo@Ex-4 were diminished upon CD4 Treg cell depletion, underscoring their role in this context. Notably, CD4 Treg cell induction correlated with the presence of species, and disruption of gut microbiota adversely affected these cells and the therapeutic efficacy of the treatment. However, the reintroduction of strains counteracted these adverse effects.
This study elucidates a novel therapeutic mechanism of Ex-4-loaded hUCMSCs exosomes in DN, highlighting the induction of CD4 Treg cells mediated by specific gut microbiota components. These findings underscore the potential of leveraging gut microbiota and immune cell interplay in developing effective DN treatments.
糖尿病肾病(DN)带来了重大的治疗挑战,复杂的病理生理机制使其更加棘手。最近的研究表明,艾塞那肽-4(Ex-4)可能是一种治疗DN的药物,但其作用机制尚不清楚。本研究旨在探讨源自人脐带间充质干细胞(hUCMSCs)的富含Ex-4的外泌体对DN的影响及其潜在机制,重点关注其肾脏保护特性以及与肠道微生物群的相互作用。
通过电穿孔法将Ex-4载入hUCMSCs的外泌体(hUCMSCs-Exo)中。采用链脲佐菌素(STZ)诱导的DN小鼠模型来评估这些工程化外泌体的治疗效果。该研究还利用生物信息学、流式细胞术进一步探究免疫细胞动态变化,主要是CD4调节性T(Treg)细胞,并通过抗生素治疗和特定细菌重新引入来研究肠道微生物群的影响。
用hUCMSCs-Exo@Ex-4治疗可显著改善关键的DN指标,包括血糖和蛋白尿,减轻肾脏损伤。观察到DN中天然Treg细胞浸润显著减少,而载有Ex-4的外泌体促进了CD4 Treg细胞的诱导。CD4 Treg细胞耗竭后,hUCMSCs-Exo@Ex-4的治疗益处减弱,突出了它们在这种情况下的作用。值得注意的是,CD4 Treg细胞的诱导与某物种的存在相关,肠道微生物群的破坏对这些细胞和治疗的疗效产生了不利影响。然而,重新引入某些菌株可抵消这些不利影响。
本研究阐明了载有Ex-4的hUCMSCs外泌体在DN中的一种新的治疗机制,强调了由特定肠道微生物群成分介导的CD4 Treg细胞的诱导。这些发现突出了利用肠道微生物群和免疫细胞相互作用来开发有效DN治疗方法的潜力。