Roles for epithelial integrin α3β1 in regulation of the microenvironment during normal and pathological tissue remodeling

被引:3
|
作者
Miskin, Rakshitha Pandulal [1 ]
DiPersio, C. Michael [2 ,3 ]
机构
[1] Nanite Inc, Boston, MA 02109 USA
[2] Albany Med Coll, Dept Surg, Albany, NY 12208 USA
[3] Albany Med Coll, Dept Mol & Cellular Physiol, Albany, NY 12208 USA
来源
基金
美国国家卫生研究院;
关键词
alternative polyadenylation; alternative splicing; integrin alpha 3 beta 1; secretome; tissue microenvironment; MESSENGER-RNA STABILITY; INTERSTITIAL LUNG-DISEASE; BREAST-CANCER CELLS; CRUCIAL ROLE; POSTTRANSCRIPTIONAL REGULATION; TUMOR MICROENVIRONMENT; TRANSCRIPTION FACTORS; EXTRACELLULAR-MATRIX; ANGIOGENESIS; ADHESION;
D O I
10.1152/ajpcell.00128.2024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Integrin receptors for the extracellular matrix activate intracellular signaling pathways that are critical for tissue development, homeostasis, and regeneration/repair, and their loss or dysregulation contributes to many developmental defects and tissue pathologies. This review will focus on tissue remodeling roles for integrin alpha 3 beta 1, a receptor for laminins found in the basement membranes (BMs) that underlie epithelial cell layers. As a paradigm, we will discuss literature that supports a role for alpha 3 beta 1 in promoting ability of epidermal keratinocytes to modify their tissue microenvironment during skin development, wound healing, or tumorigenesis. Preclinical and clinical studies have shown that this role depends largely on ability of alpha 3 beta 1 to govern the keratinocyte's repertoire of secreted proteins, or the "secretome," including 1) matrix proteins and proteases involved in matrix remodeling and 2) paracrine-acting growth factors/cytokines that stimulate other cells with important tissue remodeling functions (e.g., endothelial cells, fibroblasts, inflammatory cells). Moreover, alpha 3 beta 1 signaling controls gene expression that helps epithelial cells carry out these functions, including genes that encode secreted matrix proteins, proteases, growth factors, or cytokines. We will review what is known about alpha 3 beta 1-dependent gene regulation through both transcription and posttranscriptional mRNA stability. Regarding the latter, we will discuss examples of alpha 3 beta 1-dependent alternative splicing (AS) or alternative polyadenylation (APA) that prevents inclusion of cis-acting mRNA sequences that would otherwise target the transcript for degradation via nonsense-mediated decay or destabilizing AU-rich elements (AREs) in the 3 '-untranslated region (3 '-UTR). Finally, we will discuss prospects and anticipated challenges of exploiting alpha 3 beta 1 as a clinical target for the treatment of cancer or wound healing.
引用
收藏
页码:C1308 / C1319
页数:12
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