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来自腹壁脂肪组织的人毛细血管内皮细胞:使用抗PECAM抗体进行分离。

Human capillary endothelial cells from abdominal wall adipose tissue: isolation using an anti-pecam antibody.

作者信息

Springhorn J P, Madri J A, Squinto S P

机构信息

Department of Molecular Development, Alexion Pharmaceuticals, Inc., New Haven, Connecticut 06511, USA.

出版信息

In Vitro Cell Dev Biol Anim. 1995 Jun;31(6):473-81. doi: 10.1007/BF02634261.

DOI:10.1007/BF02634261
PMID:8589892
Abstract

We have developed a novel isolation technique for harvesting human capillary endothelial cells. We compared the use of either Ulex Europaeus Agglutinin (UEA) lectin or anti-platelet endothelial cell adhesion molecule (PECAM) antibody conjugated to magnetic beads for the ability to isolate and maintain pure cultures of human capillary endothelial cells. Cells isolated using either method actively scavenged DiI-acetylated-low density lipoprotein and expressed von Willebrand factor (vWf) up to four passages as assessed by immunofluorescent labeling. Endothelial cells isolated using the anti-PECAM antibody method maintained these endothelial-specific properties for up to 12 passages while the percentage of UEA selected cells expressing these properties decreased during increasing passage number. Furthermore, while both techniques yielded cells that bind UEA at Passage six, only the antibody selected cells expressed the normal pattern of endothelial-specific cellular adhesion molecules as assessed by flow cytometry. Both cell isolates were cultured within a three-dimensional matrix of type I collagen, the antibody selected cells formed tubelike structures within 2 days, while the lectin selected cells did not. The antibody selected capillary endothelial cells were transduced with a retroviral vector containing the human growth hormone cDNA and were found to secrete growth hormone from both two- and three-dimensional cultures. We propose that anti-PECAM antibodies linked to a solid support provide a highly selective step in the isolation and maintenance of pure populations of human capillary endothelial cells from abdominal wall liposuction remnants.

摘要

我们开发了一种用于收获人毛细血管内皮细胞的新型分离技术。我们比较了使用欧洲荆豆凝集素(UEA)凝集素或与磁珠偶联的抗血小板内皮细胞黏附分子(PECAM)抗体来分离和维持人毛细血管内皮细胞纯培养物的能力。通过免疫荧光标记评估,使用这两种方法分离的细胞均能有效摄取DiI-乙酰化低密度脂蛋白,并表达血管性血友病因子(vWf),传代至四代。使用抗PECAM抗体方法分离的内皮细胞在传代至12代时仍保持这些内皮细胞特异性特性,而随着传代次数增加,UEA选择的表达这些特性的细胞百分比下降。此外,虽然两种技术在第六代时均产生了结合UEA的细胞,但通过流式细胞术评估,只有抗体选择的细胞表达正常模式的内皮细胞特异性细胞黏附分子。两种细胞分离物均在I型胶原三维基质中培养,抗体选择的细胞在2天内形成管状结构,而凝集素选择的细胞则未形成。用含有人生长激素cDNA的逆转录病毒载体转导抗体选择的毛细血管内皮细胞,发现其在二维和三维培养中均分泌生长激素。我们提出,与固相支持物连接的抗PECAM抗体在从腹壁吸脂残留物中分离和维持人毛细血管内皮细胞纯群体的过程中提供了一个高度选择性的步骤。

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