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来自贫血的Sl/Sld小鼠和同窝正常对照小鼠的克隆永久性基质细胞系的生物学特性

Biological characterization of cloned permanent stromal cell lines from anemic Sl/Sld mice and +/+ littermates.

作者信息

Anklesaria P, Klassen V, Sakakeeny M A, FitzGerald T J, Harrison D, Rybak M E, Greenberger J S

出版信息

Exp Hematol. 1987 Jul;15(6):636-44.

PMID:3595763
Abstract

Permanent cloned bone marrow stromal cell lines, designated Sld1, Sld2, Sld3, were derived from long-term bone marrow cultures (LTBMC) of Sl/Sld mice and littermate WCB6F1 mice (designated +/+1, +/+2, +/+1.10, and +/+2.4). Production of extracellular matrix proteins by these cell lines was detected using specific antibodies. Fibronectin, laminin, and collagen type IV were detected in all clonal cell lines tested. Each cloned stromal cell line or parent stromal cell culture was also tested in vitro for support of engrafted hemopoietic stem cells. Engrafted hemopoietic stem cells from C57BL/6J LTBMCs forming CFU-GEMM and BFUe colonies were supported at 76% and 44% efficiency by lines +/+2.4 and +/+1.10, respectively, compared to the number recovered from parent uncloned C57BL/6J stromal cell cultures. In contrast, cell lines Sld1 and Sld3 were significantly less supportive of CFU-GEMM progenitor cells (14% and 18% efficiency, respectively) and erythroid progenitors (6% and less than 0.1% efficiency, respectively). Some Sld lines also showed reduced support compared to +/+ cell lines of a clonal multipotential erythroid cell line B6SUtA. These permanent stromal cell lines should be useful in elucidation of the specific microenvironmental factors required for support of multilineage and erythroid progenitor cells.

摘要

从Sl/Sld小鼠和同窝WCB6F1小鼠(分别命名为+/+1、+/+2、+/+1.10和+/+2.4)的长期骨髓培养物(LTBMC)中获得了永久克隆的骨髓基质细胞系,命名为Sld1、Sld2、Sld3。使用特异性抗体检测这些细胞系产生细胞外基质蛋白的情况。在所有测试的克隆细胞系中均检测到纤连蛋白、层粘连蛋白和IV型胶原。还对每个克隆的基质细胞系或亲代基质细胞培养物进行了体外测试,以评估其对植入的造血干细胞的支持能力。与从未克隆的亲代C57BL/6J基质细胞培养物中回收的数量相比,来自C57BL/6J LTBMCs形成CFU-GEMM和BFUe集落的植入造血干细胞分别以76%和44%的效率得到+/+2.4和+/+1.10细胞系的支持。相比之下,细胞系Sld1和Sld3对CFU-GEMM祖细胞(分别为14%和18%的效率)和红系祖细胞(分别为6%和低于0.1%的效率)的支持能力明显较低。与克隆的多能红系细胞系B6SUtA的+/+细胞系相比,一些Sld细胞系的支持能力也有所降低。这些永久基质细胞系在阐明支持多谱系和红系祖细胞所需的特定微环境因素方面应具有重要作用。

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