Por favor, use este identificador para citar o enlazar este Item:http://hdl.handle.net/20.500.12105/6676
Título
Transient fibrosis resolves via fibroblast inactivation in the regenerating zebrafish heart
Autor(es)
Sanchez-Iranzo, Hector CNIC | Galardi-Castilla, Maria CNIC | Sanz-Morejon, Andres CNIC | Gonzalez-Rosa, Juan Manuel CNIC | Costa, Ricardo CNIC | Ernst, Alexander | Sainz de Aja, Julio CNIC | Langa, Xavier | Mercader, Nadia CNIC
Fecha de publicación
2018
Cita
Proc Natl Acad Sci U S A. 2018; 115(16):4188-93
Idioma
Inglés
Tipo de documento
journal article
Resumen
In the zebrafish (Danio rerio), regeneration and fibrosis after cardiac injury are not mutually exclusive responses. Upon cardiac cryoinjury, collagen and other extracellular matrix (ECM) proteins accumulate at the injury site. However, in contrast to the situation in mammals, fibrosis is transient in zebrafish and its regression is concomitant with regrowth of the myocardial wall. Little is known about the cells producing this fibrotic tissue or how it resolves. Using novel genetic tools to mark periostin b- and collagen 1alpha2 (col1a2)-expressing cells in combination with transcriptome analysis, we explored the sources of activated fibroblasts and traced their fate. We describe that during fibrosis regression, fibroblasts are not fully eliminated but become inactivated. Unexpectedly, limiting the fibrotic response by genetic ablation of col1a2-expressing cells impaired cardiomyocyte proliferation. We conclude that ECMproducing cells are key players in the regenerative process and suggest that antifibrotic therapies might be less efficient than strategies targeting fibroblast inactivation.
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- Microsoft Excel 2007