Matrix stiffness- dependent regulation of immunomodulatory genes in human MSCs is associated with the lncRNA CYTOR

• 成果类型: Article
• 署名作者: Lim, Justin J.; Vining, Kyle H.; Mooney, David J.; Blencowe, Benjamin J.
• 署名单位: University of Toronto; University of Toronto; University of Pennsylvania; University of Pennsylvania; Harvard University; Harvard University
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-13025
• DOI: 10.1073/pnas.2404146121
• 发表日期: 2024-08-06
• 关键词: substrate stiffness; stem-cells; activator protein-1; reveals; microenvironment; viscoelasticity; expression; migration; kinase; modes

摘要

Cell-matrix interactions in 3D environments significantly differ from those in 2D cultures. As such, mechanisms of mechanotransduction in 2D cultures are not necessarily applicable to cell- encapsulating hydrogels that resemble features of tissue architecture. Accordingly, the characterization of molecular pathways in 3D matrices is expected to uncover insights into how cells respond to their mechanical environment in physiological contexts, and potentially also inform hydrogel-based strategies in cell therapies. In this study, a bone marrow- mimetic hydrogel was employed to systematically investigate the stiffness- responsive transcriptome of mesenchymal stromal cells. High matrix rigidity impeded integrin- collagen adhesion, resulting in changes in cell morphology characterized by a contractile network of actin proximal to the cell membrane. This resulted in a suppression of extracellular matrix- regulatory genes involved in the remodeling of collagen fibrils, as well as the upregulation of secreted immunomodulatory factors. Moreover, an investigation of long noncoding RNAs revealed that the cytoskeleton regulator RNA (CYTOR) contributes to these 3D stiffness- driven changes in gene expression. Knockdown of CYTOR using antisense oligonucleotides enhanced the expression of numerous mechanoresponsive cytokines and chemokines to levels exceeding those achievable by modulating matrix stiffness alone. Taken together, our findings further our understanding of mechanisms of mechanotransduction that are distinct from canonical mechanotransductive pathways observed in 2D cultures.