Guo Qiusha, Xia Bing, Moshiach Simon, Xu Congfeng, Jiang Yongde, Chen Yuanjian, Sun Yao, Lahti Jill M, Zhang Xin A
Department of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Eur J Cell Biol. 2008 Apr;87(4):251-66. doi: 10.1016/j.ejcb.2007.11.004. Epub 2008 Jan 8.
Although epithelial morphogenesis is tightly controlled by intrinsic genetic programs, the microenvironment in which epithelial cells proliferate and differentiate also contributes to the morphogenetic process. The roles of the physical microenvironment in epithelial morphogenesis, however, have not been well dissected. In this study, we assessed the impact of the microenvironment on epithelial cyst formation, which often marks the beginning or end step of morphogenesis of epithelial tissues and the pathological characteristic of some diseases. Previous studies have demonstrated that Madin-Darby canine kidney (MDCK) epithelial cells form cysts when grown in a three-dimensional (3D) extracellullar matrix (ECM) environment. We have now further demonstrated that the presence of ECM in the 3D scaffold is required for the formation of properly polarized cysts. Also, we have found that the full interface of epithelial cells with the ECM environment (in-3D) is not essential for cyst formation, since partial contact (on-3D) is sufficient to induce cystogenesis. In addition, we have defined the minimal ECM environment or the physical threshold for cystogenesis under the on-3D condition. Only above the threshold can the morphological cues from the ECM environment induce cyst formation. Moreover, cyst formation under the on-3D condition described in this study defines a novel and more feasible model to analyze in vitro morphogenesis. Finally, we have found that, during cystogenesis, MDCK cells generate basal microprotrusions and produce vesicle-like structures to the basal extracellular space, which are specific to and correlated with cyst formation. For the first time, we have systematically and quantitatively elucidated the microenvironmental determinants for epithelial cystogenesis.
尽管上皮形态发生受到内在遗传程序的严格控制,但上皮细胞增殖和分化所处的微环境也对形态发生过程有贡献。然而,物理微环境在上皮形态发生中的作用尚未得到充分剖析。在本研究中,我们评估了微环境对上皮囊肿形成的影响,上皮囊肿形成常常标志着上皮组织形态发生的起始或终结步骤以及某些疾病的病理特征。先前的研究表明,Madin-Darby犬肾(MDCK)上皮细胞在三维(3D)细胞外基质(ECM)环境中生长时会形成囊肿。我们现在进一步证明,3D支架中ECM的存在是形成正确极化囊肿所必需的。此外,我们发现上皮细胞与ECM环境的完全界面(在3D中)对于囊肿形成并非必不可少,因为部分接触(在3D上)就足以诱导囊肿形成。另外,我们已经确定了在“在3D上”条件下囊肿形成的最小ECM环境或物理阈值。只有高于该阈值,来自ECM环境的形态学线索才能诱导囊肿形成。而且,本研究中描述的“在3D上”条件下的囊肿形成定义了一种新颖且更可行的体外形态发生分析模型。最后,我们发现,在囊肿形成过程中,MDCK细胞产生基底微突起并向基底细胞外空间产生囊泡样结构,这些结构是囊肿形成所特有的且与之相关。我们首次系统地、定量地阐明了上皮囊肿形成的微环境决定因素。