The mesenchymal cell, its role in the embryo, and the remarkable signaling mechanisms that create it - PubMed
Review
. 2005 Jul;233(3):706-20.
doi: 10.1002/dvdy.20345.
Affiliations
- PMID: 15937929
- DOI: 10.1002/dvdy.20345
Free article
Review
The mesenchymal cell, its role in the embryo, and the remarkable signaling mechanisms that create it
Elizabeth D Hay. Dev Dyn. 2005 Jul.
Free article
Abstract
This review centers on the role of the mesenchymal cell in development. The creation of this cell is a remarkable process, one where a tightly knit, impervious epithelium suddenly extends filopodia from its basal surface and gives rise to migrating cells. The ensuing process of epithelial-mesenchymal transformation (EMT) creates the mechanism that makes it possible for the mesenchymal cell to become mobile, so as to leave the epithelium and move through the extracellular matrix. EMT is now recognized as a very important mechanism for the remodeling of embryonic tissues, with the power to turn an epithelial somite into sclerotome mesenchyme, and the neural crest into mesenchyme that migrates to many targets. Thus, the time has come for serious study of the underlying mechanisms and the signaling pathways that are used to form the mesenchymal cell in the embryo. In this review, I discuss EMT centers in the embryo that are ready for such serious study and review our current understanding of the mechanisms used for EMT in vitro, as well as those that have been implicated in EMT in vivo. The purpose of this review is not to describe every study published in this rapidly expanding field but rather to stimulate the interest of the reader in the study of the role of the mesenchymal cell in the embryo, where it plays profound roles in development. In the adult, mesenchymal cells may give rise to metastatic tumor cells and other pathological conditions that we will touch on at the end of the review.
Similar articles
-
Epithelial to mesenchymal transition during gastrulation: an embryological view.
Nakaya Y, Sheng G. Nakaya Y, et al. Dev Growth Differ. 2008 Dec;50(9):755-66. doi: 10.1111/j.1440-169X.2008.01070.x. Dev Growth Differ. 2008. PMID: 19046163 Review.
-
Chang JY, Wright JM, Svoboda KK. Chang JY, et al. Cells Tissues Organs. 2007;185(1-3):40-7. doi: 10.1159/000101301. Cells Tissues Organs. 2007. PMID: 17587806 Review.
-
Nawshad A, LaGamba D, Hay ED. Nawshad A, et al. Arch Oral Biol. 2004 Sep;49(9):675-89. doi: 10.1016/j.archoralbio.2004.05.007. Arch Oral Biol. 2004. PMID: 15275855 Review.
Cited by
-
Xiu M, Liu YH, Brigstock DR, He FH, Zhang RJ, Gao RP. Xiu M, et al. World J Gastroenterol. 2012 Dec 21;18(47):7070-8. doi: 10.3748/wjg.v18.i47.7070. World J Gastroenterol. 2012. PMID: 23323010 Free PMC article.
-
Transcription factor Sp3 knockout mice display serious cardiac malformations.
van Loo PF, Mahtab EA, Wisse LJ, Hou J, Grosveld F, Suske G, Philipsen S, Gittenberger-de Groot AC. van Loo PF, et al. Mol Cell Biol. 2007 Dec;27(24):8571-82. doi: 10.1128/MCB.01350-07. Epub 2007 Oct 8. Mol Cell Biol. 2007. PMID: 17923686 Free PMC article.
-
Karamichos D, Lakshman N, Petroll WM. Karamichos D, et al. Invest Ophthalmol Vis Sci. 2007 Nov;48(11):5030-7. doi: 10.1167/iovs.07-0443. Invest Ophthalmol Vis Sci. 2007. PMID: 17962454 Free PMC article.
-
Phenotypic transition of the collecting duct epithelium in congenital urinary tract obstruction.
Trnka P, Hiatt MJ, Ivanova L, Tarantal AF, Matsell DG. Trnka P, et al. J Biomed Biotechnol. 2010;2010:696034. doi: 10.1155/2010/696034. Epub 2009 Dec 13. J Biomed Biotechnol. 2010. PMID: 20037736 Free PMC article.
-
Ahlstrom JD, Erickson CA. Ahlstrom JD, et al. Commun Integr Biol. 2009 Nov;2(6):489-93. doi: 10.4161/cib.2.6.9406. Commun Integr Biol. 2009. PMID: 20195454 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources