Literature DB >> 29269349

Infarct Fibroblasts Do Not Derive From Bone Marrow Lineages.

Thomas Moore-Morris1, Paola Cattaneo1, Nuno Guimarães-Camboa1, Julius Bogomolovas1, Marta Cedenilla1, Indroneal Banerjee1, Mercedes Ricote1, Tatiana Kisseleva1, Lunfeng Zhang1, Yusu Gu1, Nancy D Dalton1, Kirk L Peterson1, Ju Chen1, Michel Pucéat1, Sylvia M Evans2.   

Abstract

RATIONALE: Myocardial infarction is a major cause of adult mortality worldwide. The origin(s) of cardiac fibroblasts that constitute the postinfarct scar remain controversial, in particular the potential contribution of bone marrow lineages to activated fibroblasts within the scar.
OBJECTIVE: The aim of this study was to establish the origin(s) of infarct fibroblasts using lineage tracing and bone marrow transplants and a robust marker for cardiac fibroblasts, the Collagen1a1-green fluorescent protein reporter. METHODS AND
RESULTS: Using genetic lineage tracing or bone marrow transplant, we found no evidence for collagen-producing fibroblasts derived from hematopoietic or bone marrow lineages in hearts subjected to permanent left anterior descending coronary artery ligation. In fact, fibroblasts within the infarcted area were largely of epicardial origin. Intriguingly, collagen-producing fibrocytes from hematopoietic lineages were observed attached to the epicardial surface of infarcted and sham-operated hearts in which a suture was placed around the left anterior descending coronary artery.
CONCLUSIONS: In this controversial field, our study demonstrated that the vast majority of infarct fibroblasts were of epicardial origin and not derived from bone marrow lineages, endothelial-to-mesenchymal transition, or blood. We also noted the presence of collagen-producing fibrocytes on the epicardial surface that resulted at least in part from the surgical procedure.
© 2017 American Heart Association, Inc.

Entities:  

Keywords:  bone marrow; fibroblasts; fibrosis; heart diseases; myocardial infarction

Mesh:

Substances:

Year:  2017        PMID: 29269349      PMCID: PMC5815911          DOI: 10.1161/CIRCRESAHA.117.311490

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


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