Fibroblast growth factor (FGF)-4 can induce proliferation of cardiac cushion mesenchymal cells during early valve leaflet formation - PubMed (original) (raw)
Fibroblast growth factor (FGF)-4 can induce proliferation of cardiac cushion mesenchymal cells during early valve leaflet formation
Yukiko Sugi et al. Dev Biol. 2003.
Free article
Abstract
While much has been learned about how endothelial cells transform to mesenchyme during cardiac cushion formation, there remain fundamental questions about the developmental fate of cushions. In the present work, we focus on the growth and development of cushion mesenchyme. We hypothesize that proliferative expansion and distal elongation of cushion mesenchyme mediated by growth factors are the basis of early valve leaflet formation. As a first step to test this hypothesis, we have localized fibroblast growth factor (FGF)-4 protein in cushion mesenchymal cells at the onset of prevalve leaflet formation in chick embryos (Hamburger and Hamilton stage 20-25). Ligand distribution was correlated with FGF receptor (FGFR) expression. In situ hybridization data indicated that FGFR3 mRNA was confined to the endocardial rim of the atrioventricular (AV) cushion pads, whereas FGFR2 was expressed exclusively in cushion mesenchymal cells. FGFR1 expression was detected in both endocardium and cushion mesenchyme as well as in myocardium. To determine whether the FGF pathways play regulatory roles in cushion mesenchymal cell proliferation and elongation into prevalvular structure, FGF-4 protein was added to the cushion mesenchymal cells explanted from stage 24-25 chick embryos. A significant increase in proliferative ability was strongly suggested in FGF-4-treated mesenchymal cells as judged by the incorporation of 5'-bromodeoxyuridine (BrdU). To determine whether cushion cells responded similarly in vivo, a replication-defective retrovirus encoding FGF-4 with the reporter, bacterial beta-galactosidase was microinjected into stage 18 chick cardiac cushion mesenchyme along the inner curvature where AV and outflow cushions converge. As compared with vector controls, overexpression of FGF-4 clearly induced expansion of cushion mesenchyme toward the lumen. To further test the proliferative effect of FGF-4 in cardiac cushion expansion in vivo (ovo), FGF-4 protein was microinjected into stage 18 chick inner curvature. An assay for BrdU incorporation indicated a significant increase in proliferative ability in FGF-4 microinjected cardiac cushion mesenchyme as compared with BSA-microinjected controls. Together, these results suggest a role of FGF-4 for cardiac valve leaflet formation through proliferative expansion of cushion mesenchyme.
Similar articles
- Fibroblast growth factor-2 stimulates embryonic cardiac mesenchymal cell proliferation.
Choy M, Oltjen SL, Otani YS, Armstrong MT, Armstrong PB. Choy M, et al. Dev Dyn. 1996 Jun;206(2):193-200. doi: 10.1002/(SICI)1097-0177(199606)206:2<193::AID-AJA8>3.0.CO;2-D. Dev Dyn. 1996. PMID: 8725286 - Bone morphogenetic protein-2 can mediate myocardial regulation of atrioventricular cushion mesenchymal cell formation in mice.
Sugi Y, Yamamura H, Okagawa H, Markwald RR. Sugi Y, et al. Dev Biol. 2004 May 15;269(2):505-18. doi: 10.1016/j.ydbio.2004.01.045. Dev Biol. 2004. PMID: 15110716 - Molecular regulation of atrioventricular valvuloseptal morphogenesis.
Eisenberg LM, Markwald RR. Eisenberg LM, et al. Circ Res. 1995 Jul;77(1):1-6. doi: 10.1161/01.res.77.1.1. Circ Res. 1995. PMID: 7788867 Review. - Angiogenic modulators in valve development and disease: does valvular disease recapitulate developmental signaling pathways?
Shworak NW. Shworak NW. Curr Opin Cardiol. 2004 Mar;19(2):140-6. doi: 10.1097/00001573-200403000-00013. Curr Opin Cardiol. 2004. PMID: 15075741 Review.
Cited by
- Atrioventricular valve development: new perspectives on an old theme.
de Vlaming A, Sauls K, Hajdu Z, Visconti RP, Mehesz AN, Levine RA, Slaugenhaupt SA, Hagège A, Chester AH, Markwald RR, Norris RA. de Vlaming A, et al. Differentiation. 2012 Jul;84(1):103-16. doi: 10.1016/j.diff.2012.04.001. Epub 2012 May 11. Differentiation. 2012. PMID: 22579502 Free PMC article. Review. - Genomic analysis distinguishes phases of early development of the mouse atrio-ventricular canal.
Vrljicak P, Chang AC, Morozova O, Wederell ED, Niessen K, Marra MA, Karsan A, Hoodless PA. Vrljicak P, et al. Physiol Genomics. 2010 Feb 4;40(3):150-7. doi: 10.1152/physiolgenomics.00142.2009. Epub 2009 Dec 1. Physiol Genomics. 2010. PMID: 19952280 Free PMC article. - VGLL4 plays a critical role in heart valve development and homeostasis.
Yu W, Ma X, Xu J, Heumüller AW, Fei Z, Feng X, Wang X, Liu K, Li J, Cui G, Peng G, Ji H, Li J, Jing N, Song H, Lin Z, Zhao Y, Wang Z, Zhou B, Zhang L. Yu W, et al. PLoS Genet. 2019 Feb 21;15(2):e1007977. doi: 10.1371/journal.pgen.1007977. eCollection 2019 Feb. PLoS Genet. 2019. PMID: 30789911 Free PMC article. - Mitogen-activated protein kinase signaling in the heart: angels versus demons in a heart-breaking tale.
Rose BA, Force T, Wang Y. Rose BA, et al. Physiol Rev. 2010 Oct;90(4):1507-46. doi: 10.1152/physrev.00054.2009. Physiol Rev. 2010. PMID: 20959622 Free PMC article. Review. - The FGF family: biology, pathophysiology and therapy.
Beenken A, Mohammadi M. Beenken A, et al. Nat Rev Drug Discov. 2009 Mar;8(3):235-53. doi: 10.1038/nrd2792. Nat Rev Drug Discov. 2009. PMID: 19247306 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous