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Secreted Frizzled-related proteins can regulate metanephric development

  1. Author:
    Yoshino, K.
    Rubin, J. S.
    Higinbotham, K. G.
    Uren, A.
    Anest, V.
    Plisov, S. Y.
    Perantoni, A. O.
  2. Author Address

    NCI, Comparat Carcinogenesis Lab, Bldg 538, Room 205E, Frederick, MD 21702 USA. NCI, Comparat Carcinogenesis Lab, Frederick, MD 21702 USA. NCI, Cellular & Mol Biol Lab, Bethesda, MD 20892 USA. Yoshino K NCI, Comparat Carcinogenesis Lab, Bldg 538, Room 205E, Frederick, MD 21702 USA.
    1. Year: 2001
  1. Journal: Mechanisms of Development
    1. 102
    2. 1-2
    3. Pages: 45-55
  2. Type of Article: Article
  1. Abstract:

    Wnt-4 signaling plays a critical role in kidney development and is associated with the epithelial conversion of the metanephric mesenchyme. Furthermore, secreted Frizzled-related proteins (sFRPs) that can bind Wnts are normally expressed in the developing metanephros, and function in other systems as modulators of Wnt signaling. sfrp-1 is distributed throughout the medullary and cortical stroma in the metanephros, but is absent from condensed mesenchyme and primitive tubular epithelia of the developing nephron where wnt-1 is highly expressed. In contrast, sfrp-2 is expressed in primitive tubules. To determine their role in kidney development, recombinant sFRP-1, sFRP-2 or combinations of both were applied to cultures of 13-dpc rat metanephroi. Both tubule formation and bud branching were markedly inhibited by sFRP-1, but concurrent sFRP-2 treatment restored some tubular differentiation and bud branching, sFRP-2 itself showed no effect on cultures of metanephroi. In cultures of isolated, induced rat metanephric mesenchymes, sFRP-1 blocked events associated with epithelial conversion (tubulogenesis and expression of lim-1, sfrp-2 and E-cadherin); however, it had no demonstrable effect on early events (compaction of mesenchyme and expression of wt1). As shown herein, sFRP-1 binds Wnt-4 with considerable avidity and inhibits the DNA-binding activity of TCF, an effector of Wnt signaling, while sFRP 2 had no effect on TCF activation. These observations suggest that sFRP- 1 and sFRP-2 compete locally to regulate Wnt signaling during renal organogenesis. The antagonistic effect of sFRP-1 may be important either in preventing inappropriate development within differentiated areas of the medulla or in maintaining a population of cortical blastemal cells to facilitate further renal expansion. On the other hand, sFRP-2 might promote tubule formation by permitting Wnt-4 signaling in the presence of sFRP-1. Published by Elsevier Science Ireland Ltd.

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