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饥饿与炎症调节脂肪间充质基质细胞的分子特征。

Starvation and Inflammation Modulate Adipose Mesenchymal Stromal Cells' Molecular Signature.

作者信息

Piccolo Simona, Grieco Giulio, Visconte Caterina, De Luca Paola, Taiana Michela, Zagra Luigi, Ragni Enrico, de Girolamo Laura

机构信息

Laboratorio di Biotecnologie Applicate all'Ortopedia, IRCCS Istituto Ortopedico Galeazzi, Via Cristina Belgioioso 173, 20157 Milano, Italy.

Hip Department, IRCCS Istituto Ortopedico Galeazzi, Via Cristina Belgioioso 173, 20157 Milano, Italy.

出版信息

J Pers Med. 2024 Aug 9;14(8):847. doi: 10.3390/jpm14080847.

Abstract

Mesenchymal stromal cells (MSCs) and their released factors (secretome) are intriguing options for regenerative medicine approaches based on the management of inflammation and tissue restoration, as in joint disorders like osteoarthritis (OA). Production strategy may modulate cells and secretome fingerprints, and for the latter, the effect of serum removal by starvation used in clinical-grade protocols has been underestimated. In this work, the effect of starvation on the molecular profile of interleukin 1 beta (IL1β)-primed adipose-derived MSCs (ASCs) was tested by assessing the expression level of 84 genes related to secreted factors and 84 genes involved in defining stemness potential. After validation at the protein level, the effect of starvation modulation in the secretomes was tested in a model of OA chondrocytes. IL1β priming in vitro led to an increase in inflammatory mediators' release and reduced anti-inflammatory potential on chondrocytes, features reversed by subsequent starvation. Therefore, when applying serum removal-based clinical-grade protocols for ASCs' secretome production, the effects of starvation must be carefully considered and investigated.

摘要

间充质基质细胞(MSCs)及其释放的因子(分泌组)是再生医学方法中基于炎症管理和组织修复的有趣选择,比如在骨关节炎(OA)等关节疾病中。生产策略可能会调节细胞和分泌组特征,而对于后者,临床级方案中通过饥饿去除血清的效果一直被低估。在这项研究中,通过评估84个与分泌因子相关的基因和84个参与定义干性潜能的基因的表达水平,测试了饥饿对白细胞介素1β(IL1β)预处理的脂肪来源间充质干细胞(ASCs)分子特征的影响。在蛋白质水平验证后,在OA软骨细胞模型中测试了饥饿调节对分泌组的影响。体外IL1β预处理导致炎症介质释放增加,对软骨细胞的抗炎潜能降低,随后的饥饿可逆转这些特征。因此,在应用基于血清去除的临床级方案生产ASCs分泌组时,必须仔细考虑和研究饥饿的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b319/11355917/7c9698d5f4bb/jpm-14-00847-g001.jpg

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