Modak Rucha V, Zaiss Dietmar M
Institute of Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Bio Protoc. 2019 Nov 5;9(21). doi: 10.21769/BioProtoc.3422.
Hepatic stellate cells (HSCs), alternatively known as liver pericytes, can differentiate into myofibroblasts and secrete extra-cellular matrix components, thereby promoting wound healing and fibrosis. Studying HSCs can provide insights into the pathological mechanisms governing these processes. HSC isolation methods typically comprise of enzymatic digestion followed by density gradient centrifugation and/or Fluorescent Activated Cell Sorting (FACS) mediated sorting. In this protocol, we describe a step-wise method for HSC isolation that utilizes Pronase and Collagenase for enzymatic tissue dissociation, followed by an Optiprep based density gradient centrifugation. The isolation can be performed using common media and buffers, and without the use of any special equipment for liver perfusion and HSC isolation. The technique yields HSCs, suitable for use in assays.
肝星状细胞(HSCs),也被称为肝周细胞,可分化为肌成纤维细胞并分泌细胞外基质成分,从而促进伤口愈合和纤维化。对肝星状细胞的研究有助于深入了解这些过程的病理机制。肝星状细胞分离方法通常包括酶消化,然后进行密度梯度离心和/或荧光激活细胞分选(FACS)介导的分选。在本方案中,我们描述了一种肝星状细胞分离的逐步方法,该方法利用链霉蛋白酶和胶原酶进行酶促组织解离,随后进行基于碘克沙醇的密度梯度离心。该分离过程可使用普通培养基和缓冲液进行,无需使用任何用于肝脏灌注和肝星状细胞分离的特殊设备。该技术可获得适用于检测的肝星状细胞。