Development of the diaphragm -- a skeletal muscle essential for mammalian respiration
- PMID: 23586979
- PMCID: PMC3879042
- DOI: 10.1111/febs.12274
Development of the diaphragm -- a skeletal muscle essential for mammalian respiration
Abstract
The mammalian diaphragm muscle is essential for respiration, and thus is one of the most critical skeletal muscles in the human body. Defects in diaphragm development leading to congenital diaphragmatic hernias (CDH) are common birth defects and result in severe morbidity or mortality. Given its functional importance and the frequency of congenital defects, an understanding of diaphragm development, both normally and during herniation, is important. We review current knowledge of the embryological origins of the diaphragm, diaphragm development and morphogenesis, as well as the genetic and developmental aetiology of diaphragm birth defects.
Keywords: CDH; congenital diaphragmatic hernia; development; diaphragm; muscle; tendon.
© 2013 The Authors Journal compilation © 2013 FEBS.
Figures
Similar articles
-
Herniation through congenital diaphragmatic defects.Br J Surg. 1959 Jul;47:1-15. doi: 10.1002/bjs.18004720102. Br J Surg. 1959. PMID: 13800779 No abstract available.
-
Developmental origin and morphogenesis of the diaphragm, an essential mammalian muscle.Dev Biol. 2018 Aug 15;440(2):64-73. doi: 10.1016/j.ydbio.2018.04.010. Epub 2018 Apr 19. Dev Biol. 2018. PMID: 29679560 Free PMC article.
-
Kif7 is required for the patterning and differentiation of the diaphragm in a model of syndromic congenital diaphragmatic hernia.Proc Natl Acad Sci U S A. 2013 May 21;110(21):E1898-905. doi: 10.1073/pnas.1222797110. Epub 2013 May 6. Proc Natl Acad Sci U S A. 2013. PMID: 23650387 Free PMC article.
-
Current concepts on the pathogenesis and etiology of congenital diaphragmatic hernia.Respir Physiol Neurobiol. 2013 Nov 1;189(2):232-40. doi: 10.1016/j.resp.2013.04.015. Epub 2013 May 9. Respir Physiol Neurobiol. 2013. PMID: 23665522 Review.
-
Genetic aspects of human congenital diaphragmatic hernia.Clin Genet. 2008 Jul;74(1):1-15. doi: 10.1111/j.1399-0004.2008.01031.x. Epub 2008 May 28. Clin Genet. 2008. PMID: 18510546 Free PMC article. Review.
Cited by
-
PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects.Am J Hum Genet. 2023 Oct 5;110(10):1787-1803. doi: 10.1016/j.ajhg.2023.09.002. Epub 2023 Sep 25. Am J Hum Genet. 2023. PMID: 37751738 Free PMC article.
-
Morphofunctional Characterization of Different Tissue Factors in Congenital Diaphragmatic Hernia Affected Tissue.Diagnostics (Basel). 2021 Feb 12;11(2):289. doi: 10.3390/diagnostics11020289. Diagnostics (Basel). 2021. PMID: 33673194 Free PMC article.
-
Expression of dispatched RND transporter family member 1 is decreased in the diaphragmatic and pulmonary mesenchyme of nitrofen-induced congenital diaphragmatic hernia.Pediatr Surg Int. 2019 Jan;35(1):35-40. doi: 10.1007/s00383-018-4374-6. Epub 2018 Oct 31. Pediatr Surg Int. 2019. PMID: 30382378
-
Cellular Origin(s) of Congenital Diaphragmatic Hernia.Front Pediatr. 2021 Nov 30;9:804496. doi: 10.3389/fped.2021.804496. eCollection 2021. Front Pediatr. 2021. PMID: 34917566 Free PMC article. Review.
-
Congenital diaphragmatic hernias: from genes to mechanisms to therapies.Dis Model Mech. 2017 Aug 1;10(8):955-970. doi: 10.1242/dmm.028365. Dis Model Mech. 2017. PMID: 28768736 Free PMC article. Review.
References
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
