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Decellularized Extracellular Matrix for Cell Biology

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AbstractThe extracellular matrix (ECM) is an architecture that supports the cells in our bodies and regulates various cell functions. The ECM is composed of many proteins and carbohydrates, and these molecules activate various intracellular signaling pathways orchestrated to decide cell fates. Therefore, it is not enough to study the role of single ECM molecules to understand the roles of the ECM in the regulation of cell functions; it is necessary to understand how the ECM, as an assembly of various molecules, regulates cell functions as a whole. For this purpose, in vitro ECM models mimicking native ECM are required. Here, a decellularization technique is presented to reconstitute native ECM in vitro. In this article, methods for preparing decellularized ECM (dECM) are described for use in tumor and stem cell biology. Additionally, a method for confirmation of decellularization and a dECM modification method are described. These dECM types will be useful for comprehensive studies of ECM roles. © 2021 Wiley Periodicals LLC.Basic Protocol 1: Preparation of in vitro extracellular matrix (ECM) models mimicking native ECM in different malignant tumor tissuesBasic Protocol 2: Preparation of in vitro ECM models mimicking native ECM surrounding myoblasts differentiating into myotubes at each myogenic stageSupport Protocol 1: Confirmation of myogenic stages by myogenic stages by myogenic gene expression analysisBasic Protocol 3: Confirmation of cell removalBasic Protocol 4: Reduction of chondroitin sulfate chains in cultured cell–derived decellularized ECMSupport Protocol 2: Quantification of chondroitin sulfate chain amounts in the decellularized ECM
Title: Decellularized Extracellular Matrix for Cell Biology
Description:
AbstractThe extracellular matrix (ECM) is an architecture that supports the cells in our bodies and regulates various cell functions.
The ECM is composed of many proteins and carbohydrates, and these molecules activate various intracellular signaling pathways orchestrated to decide cell fates.
Therefore, it is not enough to study the role of single ECM molecules to understand the roles of the ECM in the regulation of cell functions; it is necessary to understand how the ECM, as an assembly of various molecules, regulates cell functions as a whole.
For this purpose, in vitro ECM models mimicking native ECM are required.
Here, a decellularization technique is presented to reconstitute native ECM in vitro.
In this article, methods for preparing decellularized ECM (dECM) are described for use in tumor and stem cell biology.
Additionally, a method for confirmation of decellularization and a dECM modification method are described.
These dECM types will be useful for comprehensive studies of ECM roles.
© 2021 Wiley Periodicals LLC.
Basic Protocol 1: Preparation of in vitro extracellular matrix (ECM) models mimicking native ECM in different malignant tumor tissuesBasic Protocol 2: Preparation of in vitro ECM models mimicking native ECM surrounding myoblasts differentiating into myotubes at each myogenic stageSupport Protocol 1: Confirmation of myogenic stages by myogenic stages by myogenic gene expression analysisBasic Protocol 3: Confirmation of cell removalBasic Protocol 4: Reduction of chondroitin sulfate chains in cultured cell–derived decellularized ECMSupport Protocol 2: Quantification of chondroitin sulfate chain amounts in the decellularized ECM.

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