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评估一种用于人上皮细胞和基质细胞培养的无血清培养基。

Evaluation of a Serum-Free Medium for Human Epithelial and Stromal Cell Culture.

机构信息

Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX, Axe Médecine Régénératrice, Centre de Recherche du CHU de Québec-Université Laval, Quebec, QC G1J 1Z4, Canada.

Centre de Recherche sur le Cancer, Université Laval, Quebec, QC G1R 3S3, Canada.

出版信息

Int J Mol Sci. 2022 Sep 2;23(17):10035. doi: 10.3390/ijms231710035.

Abstract

Over the past decade, growing demand from many domains (research, cosmetics, pharmaceutical industries, etc.) has given rise to significant expansion of the number of in vitro cell cultures. Despite the widespread use of fetal bovine serum, many issues remain. Among them, the whole constitution of most serums remains unknown and is subject to significant variations. Furthermore, the presence of potential contamination and xenogeny elements is challenging for clinical applications, while limited production is an obstacle to the growing demand. To circumvent these issues, a Serum-Free Medium (SFM) has been developed to culture dermal and vesical fibroblasts and their corresponding epithelial cells, namely, keratinocytes and urothelial cells. To assess the impact of SFM on these cells, proliferation, clonogenic and metabolic assays have been compared over three passages to conditions associated with the use of a classic Fetal Bovine Serum-Containing Medium (FBSCM). The results showed that the SFM enabled fibroblast and epithelial cell proliferation while maintaining a morphology, cell size and metabolism similar to those of FBSCM. SFM has repeatedly been found to be better suited for epithelial cell proliferation and clonogenicity. Fibroblasts and epithelial cells also showed more significant mitochondrial metabolism in the SFM compared to the FBSCM condition. However, the SFM may need further optimization to improve fibroblast proliferation.

摘要

在过去的十年中,来自许多领域(研究、化妆品、制药行业等)的需求不断增长,导致体外细胞培养的数量显著增加。尽管广泛使用胎牛血清,但仍存在许多问题。其中,大多数血清的整体成分仍然未知,并且存在很大的差异。此外,潜在的污染和异种元素的存在对临床应用构成挑战,而有限的产量则是满足不断增长的需求的障碍。为了解决这些问题,已经开发出无血清培养基(SFM)来培养真皮和膀胱成纤维细胞及其相应的上皮细胞,即角质形成细胞和尿路上皮细胞。为了评估 SFM 对这些细胞的影响,在三个传代过程中比较了增殖、集落形成和代谢测定,以评估与使用经典含胎牛血清培养基(FBSCM)相关的条件。结果表明,SFM 能够促进成纤维细胞和上皮细胞的增殖,同时保持与 FBSCM 相似的形态、细胞大小和代谢。SFM 已被反复发现更适合于上皮细胞的增殖和集落形成能力。与 FBSCM 条件相比,SFM 中的成纤维细胞和上皮细胞也显示出更显著的线粒体代谢。然而,SFM 可能需要进一步优化以提高成纤维细胞的增殖能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a841/9455993/a5adcc6268e8/ijms-23-10035-g001.jpg

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