4.7 Article

smedinx-11 is a planarian stem cell gap junction gene required for regeneration and homeostasis

Journal

DEVELOPMENT
Volume 134, Issue 17, Pages 3121-3131

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.006635

Keywords

planarian; gap junctional communication; stem cell; regeneration

Funding

  1. NCRR NIH HHS [C06 RR11244] Funding Source: Medline
  2. NICHD NIH HHS [R21 HD055850] Funding Source: Medline
  3. NIGMS NIH HHS [F32 GM078774-01A1, F32 GM078774, F32 GM078774-02] Funding Source: Medline

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The largely unknown mechanisms that regulate adult stem cells probably involve signals from neighboring differentiated cells. Gap junction channels providing direct cell-cell communication via small molecules are a crucial component of morphogenesis and normal physiology. However, no specific gap junction protein has yet been functionally linked to adult/somatic stem cell behavior in vivo or to organ regeneration. We report the identification and characterization of smedinx-11 - an innexin gap junction channel gene expressed in the adult stem cells (neoblasts) of the planarian Schmidtea mediterranea. smedinx-11 RNAi treatment inhibits regeneration and abrogates neoblast maintenance. Moreover, smedinx-11 expression is enriched in an irradiation-sensitive subpopulation('X2') and is required for proper expression of other stem cell-specific markers. Analyses of the smedinx-11 downregulation phenotype revealed a striking anterior-posterior neoblast gradient. Our data demonstrate a novel role for gap junction proteins and suggest gap junction-mediated signaling as a new and tractable control point for adult, somatic stem cell regulation.

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