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Studies of ultrastructure, gene expression, and marker analysis reveal that mouse bladder PDGFRA+ interstitial cells are fibroblasts.
Clayton, Dennis R; Ruiz, Wily G; Dalghi, Marianela G; Montalbetti, Nicolas; Carattino, Marcelo D; Apodaca, Gerard.
Afiliação
  • Clayton DR; Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Ruiz WG; Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Dalghi MG; Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Montalbetti N; Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Carattino MD; Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Apodaca G; Department of Cell Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.
Am J Physiol Renal Physiol ; 323(3): F299-F321, 2022 09 01.
Article em En | MEDLINE | ID: mdl-35834272
Fibroblasts are crucial to normal and abnormal organ and tissue biology, yet we lack basic insights into the fibroblasts that populate the bladder wall. Candidates may include bladder interstitial cells (also referred to as myofibroblasts, telocytes, and interstitial cells of Cajal-like cells), which express the fibroblast-associated marker PDGFRA along with VIM and CD34 but whose form and function remain enigmatic. By applying the latest insights in fibroblast transcriptomics, coupled with studies of gene expression, ultrastructure, and marker analysis, we observe the following: 1) that mouse bladder PDGFRA+ cells exhibit all of the ultrastructural hallmarks of fibroblasts including spindle shape, lack of basement membrane, abundant endoplasmic reticulum and Golgi, and formation of homotypic cell-cell contacts (but not heterotypic ones); 2) that they express multiple canonical fibroblast markers (including Col1a2, CD34, LY6A, and PDGFRA) along with the universal fibroblast genes Col15a1 and Pi16 but they do not express Kit; and 3) that PDGFRA+ fibroblasts include suburothelial ones (which express ACTA2, CAR3, LY6A, MYH10, TNC, VIM, Col1a2, and Col15a1), outer lamina propria ones (which express CD34, LY6A, PI16, VIM, Col1a2, Col15a1, and Pi16), intermuscular ones (which express CD34, VIM, Col1a2, Col15a1, and Pi16), and serosal ones (which express CD34, PI16, VIM, Col1a2, Col15a1, and Pi16). Collectively, our study revealed that the ultrastructure of PDFRA+ interstitial cells combined with their expression of multiple canonical and universal fibroblast-associated gene products indicates that they are fibroblasts. We further propose that there are four regionally distinct populations of fibroblasts in the bladder wall, which likely contribute to bladder function and dysfunction.NEW & NOTEWORTHY We currently lack basic insights into the fibroblasts that populate the bladder wall. By exploring the ultrastructure of mouse bladder connective tissue cells, combined with analyses of their gene and protein expression, our study revealed that PDGRA+ interstitial cells (also referred to as myofibroblasts, telocytes, and interstitial cells of Cajal-like cells) are fibroblasts and that the bladder wall contains multiple, regionally distinct populations of these cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Intersticiais de Cajal Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Intersticiais de Cajal Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article