发布: 2013年10月05日第3卷第19期 DOI: 10.21769/BioProtoc.930 浏览次数: 14176
评审: Lin FangFanglian HeAnonymous reviewer(s)
Abstract
Normal pancreatic acinar cells are difficult to maintain on traditional plastic culture surfaces due to their physical properties of housing large quantities of digestive enzymes and the formation of intercellular tight junctions and gap junctions (Apte and Wilson 2005; Rukstalis et al., 2003). However, placing primary acinar cells within a 3-dimensional matrix (3D-culture) maintains the cells for sufficient time so that they can be monitored for physiological changes to different stimuli. We have used a modified collagen 3D-culture system that has been adapted from Means et al. (2005) to model the very early events associated with pancreatic cancer development. In this model, KrasG12D-expressing pancreatic acinar cells, or wildtype acinar cells treated with EGFR-dependent growth factors (i.e., TGFα), convert to ductal cysts that mimic the acinar-to-ductal metaplasia (ADM) stage that precedes formation of Pancreatic Intraepithelial Neoplasia (PanIN) and Pancreatic Ductal Adenocarcinoma (PDAC) (Means et al., 2005; Shi et al., 2013).
Keywords: Tissue culture (组织文化)Materials and Reagents
Equipment
Procedure
文章信息
版权信息
© 2013 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Qu, C. and Konieczny, S. F. (2013). Pancreatic Acinar Cell 3-Dimensional Culture. Bio-protocol 3(19): e930. DOI: 10.21769/BioProtoc.930.
分类
癌症生物学 > 通用技术 > 细胞生物学试验
细胞生物学 > 细胞分离和培养 > 3D细胞培养
细胞生物学 > 组织分析 > 组织分离
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