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从羊脐带华通氏胶中衍生间充质基质细胞。

Derivation of Mesenchymal Stromal Cells from Ovine Umbilical Cord Wharton's Jelly.

机构信息

Servei de Teràpia Cel·lular, Banc de Sang i Teixits, Edifici Dr. Frederic Duran i Jordà, Passeig Taulat, Barcelona, Spain.

Musculoskeletal Tissue Engineering Group, Vall d'Hebron Research Institute (VHIR), Universitat Autònoma de Barcelona, Passeig de la Vall d'Hebron, Barcelona, Spain.

出版信息

Curr Protoc. 2021 Jan;1(1):e18. doi: 10.1002/cpz1.18.

Abstract

The methods described herein allow for the isolation and expansion of fibroblastic-like ovine Wharton's jelly-derived mesenchymal stromal cells (oWJ-MSC) that, similarly to their human counterparts, adhere to standard plastic surfaces in culture; show a mesenchymal profile for specific surface antigens (i.e., positive for CD44 and CD166); and lack expression of endothelial (CD31) and hematopoietic (CD45) markers as well as major histocompatibility complex (MHC) class-II. Homogeneous cell cultures result from a two-phase bioprocess design that starts with the isolation of mesenchymal stromal cells (MSC) from the Wharton's jelly of ovine umbilical cords up to a first step of cryopreservation. The second phase allows for further expansion of ovine WJ-MSC up to sufficient numbers for further studies. Overall, this methodology encompasses a 2-week bioprocess design that encompasses two cell culture passages ensuring sufficient cells for the generation of a Master Cell Bank. Further thawing and scale expansion results in large quantities of oWJ-MSC that can be readily used in proof of efficacy and safety studies in the preclinical development stage of the development of cell-based medicines. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Isolation and expansion of ovine mesenchymal stromal cells from Wharton's jelly of the umbilical cord Basic Protocol 2: Characterization of ovine mesenchymal stromal cells Basic Protocol 3: Growth profile determination of ovine mesenchymal stromal cells from Wharton's jelly.

摘要

本文所述方法允许分离和扩增纤维样绵羊华通氏胶衍生间充质基质细胞(oWJ-MSC),类似于它们的人类对应物,在培养中附着于标准塑料表面;表现出特定表面抗原的间充质特征(即,CD44 和 CD166 阳性);并且缺乏内皮(CD31)和造血(CD45)标志物以及主要组织相容性复合体(MHC)II 类的表达。均相细胞培养源自两相生物工艺设计,该设计从绵羊脐带华通氏胶中分离间充质基质细胞(MSC)开始,直至第一步冷冻保存。第二阶段允许进一步扩增绵羊 WJ-MSC,直至获得足够数量进行进一步研究。总体而言,该方法学包括 2 周的生物工艺设计,包括两个细胞培养传代,以确保有足够的细胞生成主细胞库。进一步解冻和规模扩大可产生大量的 oWJ-MSC,可在细胞药物临床前开发阶段的疗效和安全性研究中轻松使用。©2021 威立出版公司。基本方案 1:从脐带华通氏胶中分离和扩增绵羊间充质基质细胞基本方案 2:绵羊间充质基质细胞的表征基本方案 3:从华通氏胶中分离的绵羊间充质基质细胞的生长曲线测定

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