Literature DB >> 8405677

Modulation of HGF-induced tubulogenesis and branching by multiple phosphorylation mechanisms.

O F Santos1, L A Moura, E M Rosen, S K Nigam.   

Abstract

MDCK cells cultured in Type I collagen gels can be induced to develop branching tubular structures with demonstrable lumens in the presence of hepatocyte growth factor (HGF). As we have now shown by immunofluorescent localization of specific marker proteins, these tubules retain apical-basolateral polarity. However, the secondary signaling events which lead to these characteristic morphogenetic changes induced by HGF remain largely unelucidated. In order to examine these signaling events, particularly the role of protein phosphorylation in the formation of branching tubular structures, Madin-Darby canine kidney (MDCK) cells in collagen gels were treated with HGF plus well-characterized agents that affect protein phosphorylation. We quantified the formation of branching processes, an early step in the development of tubular structures in this model. Protein kinase C (PKC) inhibition resulted in more complex branching processes in the presence of HGF, when compared with HGF alone. In contrast, treatment with activators of protein kinase A (PKA), as well as calmodulin antagonists, caused a marked decline in process formation. Consistent with an important role for protein phosphorylation in HGF-induced morphogenesis, protein phosphatase inhibition by okadaic acid or calyculin A was found to markedly inhibit process formation. Tyrosine kinase (TK) inhibition also decreased the percentage of processes. This is consistent with data indicating that one of the HGF receptors is identical to the c-met protooncogene product, which is known to possess TK activity. Our results suggest that the HGF-mediated induction of branching processes in MDCK cells, an early step in the development of branching tubular structures, can be modulated by multiple phosphorylation mechanisms including those mediated by PKC, PKA, and Ca2+/calmodulin-dependent kinase(s). We discuss how these phosphorylation events may play crucial roles in determining the degree of tubule formation and their length, as well as the extent of their arborization during the early development of epithelial tissues.

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Year:  1993        PMID: 8405677     DOI: 10.1006/dbio.1993.1262

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  23 in total

1.  Exocyst is involved in cystogenesis and tubulogenesis and acts by modulating synthesis and delivery of basolateral plasma membrane and secretory proteins.

Authors:  J H Lipschutz; W Guo; L E O'Brien; Y H Nguyen; P Novick; K E Mostov
Journal:  Mol Biol Cell       Date:  2000-12       Impact factor: 4.138

2.  Pak1 regulates branching morphogenesis in 3D MDCK cell culture by a PIX and beta1-integrin-dependent mechanism.

Authors:  Michael P Hunter; Mirjam M Zegers
Journal:  Am J Physiol Cell Physiol       Date:  2010-03-24       Impact factor: 4.249

3.  An in vitro tubulogenesis system using cell lines derived from the embryonic kidney shows dependence on multiple soluble growth factors.

Authors:  H Sakurai; E J Barros; T Tsukamoto; J Barasch; S K Nigam
Journal:  Proc Natl Acad Sci U S A       Date:  1997-06-10       Impact factor: 11.205

4.  Protein kinase A regulates GDNF/RET-dependent but not GDNF/Ret-independent ureteric bud outgrowth from the Wolffian duct.

Authors:  James B Tee; Yohan Choi; Mita M Shah; Ankur Dnyanmote; Derina E Sweeney; Tom F Gallegos; Kohei Johkura; Chiharu Ito; Kevin T Bush; Sanjay K Nigam
Journal:  Dev Biol       Date:  2010-09-15       Impact factor: 3.582

5.  Growth factor-dependent branching of the ureteric bud is modulated by selective 6-O sulfation of heparan sulfate.

Authors:  Mita M Shah; Hiroyuki Sakurai; Thomas F Gallegos; Derina E Sweeney; Kevin T Bush; Jeffrey D Esko; Sanjay K Nigam
Journal:  Dev Biol       Date:  2011-05-11       Impact factor: 3.582

6.  Differential tubulogenic and branching morphogenetic activities of growth factors: implications for epithelial tissue development.

Authors:  E J Barros; O F Santos; K Matsumoto; T Nakamura; S K Nigam
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-09       Impact factor: 11.205

7.  Novel Madin Darby canine kidney cell clones exhibit unique phenotypes in response to morphogens.

Authors:  S A Orellana; C D Neff; W E Sweeney; E D Avner
Journal:  In Vitro Cell Dev Biol Anim       Date:  1996-06       Impact factor: 2.416

8.  Epithelial morphogenesis of MDCK cells in three-dimensional collagen culture is modulated by interleukin-8.

Authors:  Erika K Wells; OrLando Yarborough; Richard P Lifton; Lloyd G Cantley; Michael J Caplan
Journal:  Am J Physiol Cell Physiol       Date:  2013-03-13       Impact factor: 4.249

9.  Transforming growth factor-beta signaling-deficient fibroblasts enhance hepatocyte growth factor signaling in mammary carcinoma cells to promote scattering and invasion.

Authors:  Nikki Cheng; Anna Chytil; Yu Shyr; Alison Joly; Harold L Moses
Journal:  Mol Cancer Res       Date:  2008-10       Impact factor: 5.852

10.  Microscopic analysis of the cellular events during scatter factor/hepatocyte growth factor-induced epithelial tubulogenesis.

Authors:  M J Williams; P Clark
Journal:  J Anat       Date:  2003-11       Impact factor: 2.610

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