发布: 2018年09月20日第8卷第18期 DOI: 10.21769/BioProtoc.3021 浏览次数: 8895
评审: Jia LiSalah BoudjadiYoshihiro Adachi
Abstract
The collagen contraction assay is an in vitro, three-dimensional method to determine the factor(s) affecting the contractile behavior of activated cells such as fibroblasts in either physiological or pathological scenarios. The collagen lattices/hydrogels are seeded with fibroblasts to mimic the interactions between these cells and their surrounding extracellular matrix proteins in the connective tissue. This method is an important platform to assess components as potential therapeutic targets to prevent pathologies such as fibrosis, which are manifestations of hyperactivated fibroblasts. We have described a basic version of this collagen contraction assay, which is amenable to customization using different cell types under diverse experimental conditions.
Keywords: Collagen contraction (胶原收缩)Background
Tissue contraction and remodeling of the extracellular matrix are essential processes in numerous physiological conditions such as wound healing. Central to these two phenomena are fibroblasts, which not only produce and secrete the extracellular matrix proteins but can also reorganize them through mechanical interactions. Interestingly, these cellular behaviors are often exaggerated in pathological conditions such as fibrosis (Desmoulière et al., 2005), thereby illustrating the need to understand the molecular regulation of these processes. Though it has long been known that collagen, one of the main components of the extracellular matrix, is a major player in tissue contraction (Bell et al., 1979), a thorough understanding of the mechanistic details of this process remain elusive. The study of the contraction of fibroblast populated collagen matrices in vitro has enabled researchers to identify novel players which bring about tissue contraction (Ngo et al., 2006; Su and Chen, 2015). Based on this assay, soluble factors such as TGFβ (Levi-Schaffer et al., 1999) and those from immune cells (Garbuzenko et al., 2002; Zagai et al., 2004) have been identified as major factors affecting fibroblast activity. To a large extent, relative to soluble extracellular signals, the contribution of cell-cell interactions on the contractile ability of fibroblasts has been understudied. Recently, we have shown that an important player regulating fibroblast-mediated contraction is the heterotypic cell-cell interactions with immune cells such as mast cells (Pincha et al., 2018). In this protocol, we provide a method to use this assay to determine the effect of cell-cell interactions on matrix contraction. In doing so, we have elaborated upon previously published protocols (Ngo et al., 2006; Su and Chen, 2015) and provide simple alternatives to setting up the assay and the subsequent analysis of the gels. This protocol can also be modified to recapitulate the native/in vivo environments of diverse cell types to assay their regulation within their “normal” microenvironment.
Materials and Reagents
Note: The materials below can also be substituted for equivalent reagents from other companies. Cell culture media and additives will vary based on the cells to be used for the assay. For our protocol, we have used primary dermal fibroblasts from neonatal mice and the mast cell line MCP-5.
Equipment
Software
Procedure
文章信息
版权信息
© 2018 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Pincha, N., Saha, D., Bhatt, T., Zirmire, R. K. and Jamora, C. (2018). Activation of Fibroblast Contractility via Cell-Cell Interactions and Soluble Signals. Bio-protocol 8(18): e3021. DOI: 10.21769/BioProtoc.3021.
分类
发育生物学 > 形态建成 > 能动性
细胞生物学 > 基于细胞的分析方法 > 胞外微环境
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