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犬脂肪组织的基质血管成分包含间充质基质细胞亚群,这些亚群对细胞培养塑料容器表现出时间依赖性黏附。

The Stromal Vascular Fraction from Canine Adipose Tissue Contains Mesenchymal Stromal Cell Subpopulations That Show Time-Dependent Adhesion to Cell Culture Plastic Vessels.

作者信息

Scattini Gabriele, Pellegrini Martina, Severi Giulio, Cagiola Monica, Pascucci Luisa

机构信息

Department of Veterinary Medicine, University of Perugia, 06123 Perugia, Italy.

Istituto Zooprofilattico Sperimentale dell'Umbria e delle Marche "Togo Rosati", 06126 Perugia, Italy.

出版信息

Animals (Basel). 2023 Mar 27;13(7):1175. doi: 10.3390/ani13071175.

Abstract

Adipose-derived mesenchymal stromal cells (MSCs) are extensively studied in both human and veterinary medicine. Their isolation is usually performed by collagenase digestion followed by filtration and removal of nonadherent tissue remnants 48 h after seeding. We observed that waste tissue fragments contain cells that adhere belatedly to the plastic. We aimed to investigate their basic properties to speculate on the possible existence of MSC subpopulations. Adipose tissue from three dogs was enzymatically digested. Three cell populations that adhered to the culture plastic 48, 96, and 144 h after seeding were obtained. After expansion, they were analyzed by flow cytometry for MSC-positive (CD90, CD44, and CD29) and -negative (CD14, MHCII, and CD45) markers as well as for endothelial, pericyte, and smooth muscle cell markers (CD31, CD146, and alpha-SMA). Furthermore, cells were assessed for viability, doubling time, and trilineage differentiation ability. No significant differences were found between the three subpopulations. As a result, this procedure has proven to be a valuable method for dramatically improving MSCs yield. As a consequence of cell recovery optimization, the amount of tissue harvested could be reduced, and the time required to obtain sufficient cells for clinical applications could be shortened. Further studies are needed to uncover possible different functional properties.

摘要

脂肪来源的间充质基质细胞(MSCs)在人类医学和兽医学中都得到了广泛研究。其分离通常通过胶原酶消化,然后在接种后48小时进行过滤并去除非贴壁组织残余物来完成。我们观察到废弃组织碎片中含有延迟贴壁于塑料培养皿的细胞。我们旨在研究它们的基本特性,以推测MSCs亚群可能的存在情况。对三只狗的脂肪组织进行酶消化。获得了接种后48、96和144小时贴壁于培养塑料的三个细胞群体。扩增后,通过流式细胞术分析它们的MSCs阳性(CD90、CD44和CD29)和阴性(CD14、MHCII和CD45)标志物,以及内皮细胞、周细胞和平滑肌细胞标志物(CD31、CD146和α-SMA)。此外,还评估了细胞的活力、倍增时间和三系分化能力。三个亚群之间未发现显著差异。因此,该方法已被证明是一种显著提高MSCs产量的有价值方法。由于细胞回收得到优化,可减少收获的组织量,并缩短获得足够临床应用细胞所需的时间。需要进一步研究以揭示可能存在的不同功能特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7523/10093060/5cc03c1f3d2a/animals-13-01175-g001.jpg

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