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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Fibrin and Transforming Growth Factor Alpha Affect Prostatic Smooth Muscle Cell's Phenotype and Motility

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Author(s):
Osorio, Daniel A. [1] ; Consonni, Silvio R. [2] ; dos Santos, Aline M. [1, 3] ; Carvalho, Hernandes F. [1, 3]
Total Authors: 4
Affiliation:
[1] State Univ Campinas UNICAMP, Inst Biol, Dept Struct & Funct Biol, Campinas, SP - Brazil
[2] State Univ Campinas UNICAMP, Inst Biol, Dept Biochem & Tissue Biol, Campinas, SP - Brazil
[3] State Univ Campinas UNICAMP, Natl Inst Photon Appl Cell Biol, Campinas, SP - Brazil
Total Affiliations: 3
Document type: Journal article
Source: Microscopy and Microanalysis; v. 27, n. 3, p. 579-586, JUN 2021.
Web of Science Citations: 0
Abstract

Smooth muscle cells (SMCs) are dynamic and transition from a contractile to a synthetic phenotype under different circumstances. Plasma factors (fibrin and transforming growth factors, TGFs) are possible components affecting SMCs differentiation and behavior. Thus, the objective of this work was to investigate how the fibrin matrix and TGFs affect SMCs differentiation and motility behavior. SMCs invaded the fibrin gel and adopted a stellate phenotype while reducing the expression of differentiation markers (Acta2, Myh11, and Smtn). At the ultrastructural level, SMCs did not assemble a basal lamina and showed numerous blebs along the entire cell surface. This transition was not associated with changes in focal adhesion kinase (FAK) content and phosphorylation status but reflected a marked change in FAK distribution in the cytoplasm. After 48 h in culture, SMCs caused an active degradation of the fibrin gel. Additionally, we tested the SMCs response to TGFs in a cell layer wound repair assay. TGF alpha, but not TGF beta 1 or TGF beta 3, had significantly increased motility. In conclusion, prostatic SMCs present a phenotypical transition when cultured on fibrin, adopting a micro-blebbing based motility behavior and increasing migration in response to TGF alpha. (AU)

FAPESP's process: 14/50938-8 - INCT 2014: in Photonics Applied to Cell Biology
Grantee:Hernandes Faustino de Carvalho
Support Opportunities: Research Projects - Thematic Grants