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Identity and Fate of Tbx4-Expressing Cells Reveal Developmental Cell Fate Decisions in the Allantois, Limb, and External Genitalia

  1. Author:
    Naiche, L. A.
    Arora, R.
    Kania, A.
    Lewandoski, M.
    Papaioannou, V. E.
  2. Author Address

    [Arora, R; Papaioannou, VE] Columbia Univ, Dept Genet & Dev, Coll Phys & Surg, New York, NY 10032 USA. [Naiche, LA; Lewandoski, M] NCI, Canc & Dev Biol Lab, Frederick, MD 21702 USA. [Kania, A] Univ Montreal, Fac Med, Montreal, PQ H3C 3J7, Canada. [Kania, A] Inst Rech Clin Montreal, Neural Circuit Dev Lab, Montreal, PQ H2W 1R7, Canada.;Papaioannou, VE (reprint author), Columbia Univ, Dept Genet & Dev, Coll Phys & Surg, HHSC 1402,701 W 168th St, New York, NY 10032 USA;Lewandom@mail.nih.gov vep1@columbia.edu
    1. Year: 2011
    2. Date: Oct
  1. Journal: Developmental Dynamics
    1. 240
    2. 10
    3. Pages: 2290-2300
  2. Type of Article: Article
  3. ISSN: 1058-8388
  1. Abstract:

    T-box gene Tbx4 is critical for the formation of the umbilicus and the initiation of the hindlimb. Previous studies show broad expression in the allantois, hindlimb, lung and proctodeum. We have examined the expression of Tbx4 in detail and used a Tbx4-Cre line to trace the fates of Tbx4-expressing cells. Tbx4 expression and lineage reveal that various distinct appendages, such as the allantois, hindlimb, and external genitalia, all arise from a single mesenchymal expression domain. Additionally, although Tbx4 is associated primarily with the hindlimb, we find two forelimb expression domains. Most notably, we find that, despite the requirement for Tbx4 in allantoic vasculogenesis, the presumptive endothelial cells of the allantois do not express Tbx4 and lineage tracing reveals that the umbilical vasculature never expresses Tbx4. These results suggest that endothelial lineages are segregated before the onset of vasculogenesis, and demonstrate a role for the peri-vascular tissue in vasculogenesis. Developmental Dynamics 240:2290-2300, 2011. (C) 2011 Wiley-Liss, Inc.

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External Sources

  1. DOI: 10.1002/dvdy.22731
  2. WOS: 000295155100007

Library Notes

  1. Fiscal Year: FY2011-2012
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