Cloning and characterization of a novel gene promoting ureteric bud branching in the metanephros
- PMID: 14633119
- DOI: 10.1046/j.1523-1755.2003.00304.x
Cloning and characterization of a novel gene promoting ureteric bud branching in the metanephros
Abstract
Background: The ureteric buds and metanephric mesenchymal cells reciprocally induce each other's maturation during kidney development, and implicated transcription factors, secreted growth factors, and cell surface signaling peptides are critical regulators of renal branching morphogenesis. Protein kinase C (PKC) is a key enzyme in the signal transduction mechanisms in various biologic processes, including development, because it regulates growth and differentiation. Inhibition of PKC by the sphingolipid product ceramide interferes with nephron formation in the developing kidney, but the molecule that controls ureteric bud branching downstream of PKC is still unknown.
Methods: Differential display polymerase chain reaction (PCR) of metanephroi cultured with a PKC activator and inhibitor was performed. We also examined the role of a novel gene in kidney development with organ culture system.
Results: A novel gene encoding a 759 bp mRNA was identified, and we named it metanephros-derived tubulogenic factor (MTF)/L47. Inhibition of MTF with antisense oligonucleotide impaired ureteric bud branching by cultured metanephroi, and addition of recombinant MTF protein promoted ureteric bud branching in cultured metanephroi and increased cell proliferation.
Conclusion: We identified a novel molecule in developing kidney that is capable of modulating ureteric bud branching and kidney differentiation.
Comment in
-
From the ureteric bud to the penome.Kidney Int. 2003 Dec;64(6):2320-2. doi: 10.1046/j.1523-1755.2003.00397.x. Kidney Int. 2003. PMID: 14633158 No abstract available.
Similar articles
-
Activin a produced by ureteric bud is a differentiation factor for metanephric mesenchyme.J Am Soc Nephrol. 2003 Jun;14(6):1523-34. doi: 10.1097/01.asn.0000067419.86611.21. J Am Soc Nephrol. 2003. PMID: 12761253
-
Spatiotemporal regulation of morphogenetic molecules during in vitro branching of the isolated ureteric bud: toward a model of branching through budding in the developing kidney.Dev Biol. 2004 Nov 1;275(1):44-67. doi: 10.1016/j.ydbio.2004.07.022. Dev Biol. 2004. PMID: 15464572
-
Induction of ureter branching as a response to Wnt-2b signaling during early kidney organogenesis.Dev Dyn. 2001 Sep;222(1):26-39. doi: 10.1002/dvdy.1164. Dev Dyn. 2001. PMID: 11507767
-
Renal branching morphogenesis: morphogenetic and signaling mechanisms.Semin Cell Dev Biol. 2014 Dec;36:2-12. doi: 10.1016/j.semcdb.2014.07.011. Epub 2014 Jul 28. Semin Cell Dev Biol. 2014. PMID: 25080023 Review.
-
In vitro branching tubulogenesis: implications for developmental and cystic disorders, nephron number, renal repair, and nephron engineering.Kidney Int. 1998 Jul;54(1):14-26. doi: 10.1046/j.1523-1755.1998.00969.x. Kidney Int. 1998. PMID: 9648059 Review.
Cited by
-
An Update on Protein Kinases as Therapeutic Targets-Part I: Protein Kinase C Activation and Its Role in Cancer and Cardiovascular Diseases.Int J Mol Sci. 2023 Dec 18;24(24):17600. doi: 10.3390/ijms242417600. Int J Mol Sci. 2023. PMID: 38139428 Free PMC article. Review.
-
Development of new therapies, including regeneration of the kidney, for chronic kidney diseases.Clin Exp Nephrol. 2006 Jun;10(2):99-101. doi: 10.1007/s10157-006-0418-7. Clin Exp Nephrol. 2006. PMID: 16791394 Review.
-
Application of regenerative medicine for kidney diseases.Organogenesis. 2007 Jan;3(1):34-43. doi: 10.4161/org.3.1.3961. Organogenesis. 2007. PMID: 19279698 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous