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   <subfield code="a">Novel Madin Darby Canine Kidney cell clones exhibit unique phenotypes in response to morphogens</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Stephanie Orellana, Christopher Neff, William Sweeney, Ellis Avner]</subfield>
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   <subfield code="a">Summary: Novel Madin Darby Canine Kidney cell clones were isolated. These cell clones exhibit differential responsiveness to inducers of tubule or cyst formation in collagen gel culture: hepatocyte growth factor or inducers of intracellular cAMP formation, respectively. In gel culture, clone OR93.22.D6 forms cysts and responds with morphological transformation to both hepatocyte growth factor and prostaglandin E1, and is most typical of a previously described cell type except for its higher transepithelial electrical resistance. OR55.25.II20 forms tubules in culture, is unresponsive to hepatocyte growth factor, and forms prostaglandin-induced spherical cysts. OR55.28.V2 forms dense cell spheres under control conditions, is induced to form tubules by hepatocyte growth factor, and is unresponsive to prostaglandin. OR55.29 forms only cysts, and is the only clone to form domes in monolayer culture. Tubule formation induced by hepatocyte growth factor, in all clones except OR55.25.II20, is blocked by a neutralizing antibody. In defined medium, without hepatocyte growth factor or prostaglandin, OR55.25.II20 forms spontaneous tubules. This finding indicates that a tubulogenic serum factor is not responsible for the observed phenotype. Increasing prostaglandin concentrations lead to inhibition of tubule formation and increased cyst formation. This observation suggests that induction of intracellular cAMP formation negatively regulates tubule formation in these cells, and implies that cystogenesis may represent a &quot;default pathway” for impaired tubulogenesis. These observations demonstrate that some facets of renal tubulogenesis may be independent of hepatocyte growth factor, and that care must be exercised when comparing biological studies utilizing different clones.</subfield>
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   <subfield code="a">Society for In Vitro Biology, 1996</subfield>
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   <subfield code="a">nephrogenesis</subfield>
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   <subfield code="a">growth factors</subfield>
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   <subfield code="a">morphogenesis</subfield>
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   <subfield code="a">Orellana</subfield>
   <subfield code="D">Stephanie</subfield>
   <subfield code="u">Department of Pediatrics, University of Washington and Division of Nephrology, Children's Hospital and Medical Center, Seattle, Washington</subfield>
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   <subfield code="a">Neff</subfield>
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   <subfield code="u">Department of Pediatrics, University of Washington and Division of Nephrology, Children's Hospital and Medical Center, Seattle, Washington</subfield>
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   <subfield code="u">Department of Pediatrics, University of Washington and Division of Nephrology, Children's Hospital and Medical Center, Seattle, Washington</subfield>
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   <subfield code="t">In Vitro Cellular &amp; Developmental Biology - Animal</subfield>
   <subfield code="d">Springer-Verlag</subfield>
   <subfield code="g">32/6(1996-06-01), 329-339</subfield>
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   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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