Davis G E, Black S M, Bayless K J
Department of Pathology and Laboratory Medicine, Texas A&M University Health Science Center, College Station 77843-1114, USA.
In Vitro Cell Dev Biol Anim. 2000 Sep;36(8):513-9. doi: 10.1290/1071-2690(2000)036<0513:CMDHEC>2.0.CO;2.
Here, we describe assay systems that utilize serum-free defined media to evaluate capillary morphogenesis during human endothelial cell (EC) invasion of three-dimensional collagen matrices. ECs invade these matrices over a 1-3-d period to form capillary tubes. Blocking antibodies to the alpha2beta1 integrin interfere with invasion and morphogenesis while other integrin blocking antibodies do not. Interestingly, we observed increased invasion of ECs toward a population of underlying ECs undergoing morphogenesis. In addition, we have developed assays on microscope slides that display the invasion process horizontally, thereby enhancing our ability to image these events. Thus far, we have observed intracellular vacuoles that appear to regulate the formation of capillary lumens, and extensive cell processes that facilitate the interconnection of ECs during morphogenic events. These assays should enable further investigation of the morphologic steps and molecular events controlling human capillary tube formation in three-dimensional extracellular matrices.
在此,我们描述了利用无血清限定培养基来评估人内皮细胞(EC)侵入三维胶原基质过程中毛细血管形态发生的检测系统。内皮细胞在1 - 3天的时间内侵入这些基质以形成毛细血管管。针对α2β1整合素的阻断抗体可干扰侵入和形态发生,而其他整合素阻断抗体则无此作用。有趣的是,我们观察到内皮细胞向正在进行形态发生的下层内皮细胞群体的侵入增加。此外,我们已经在显微镜载玻片上开发了检测方法,可水平展示侵入过程,从而增强了我们对这些事件进行成像的能力。到目前为止,我们已经观察到似乎调节毛细血管腔形成的细胞内液泡,以及在形态发生事件中促进内皮细胞相互连接的广泛细胞突起。这些检测方法应能进一步研究在三维细胞外基质中控制人毛细血管管形成的形态学步骤和分子事件。