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Analysis of cardiovascular anomalies in the Hoxa3 and Pax-3 homozygous null mutant mice.

Research Project

Project/Area Number 14570026
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General anatomy (including Histology/Embryology)
Research InstitutionKitasato University

Principal Investigator

KAMEDA Yoko  Kitasato Univ. School of Medicine, Department of Anatomy, Professor, 医学部, 教授 (10032898)

Co-Investigator(Kenkyū-buntansha) ARAI Yuta  Kitasato Univ. School of Medicine, Department of Anatomy, Research Associate, 医学部, 助手 (60329026)
MIURA Masaaki  Kitasato Univ. School of Medicine, Department of Anatomy, Research Associate, 医学部, 助手 (60276053)
Project Period (FY) 2002 – 2003
Project Status Completed (Fiscal Year 2003)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2003: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2002: ¥2,100,000 (Direct Cost: ¥2,100,000)
KeywordsHoxa3 knockout mice / Connexin43-LacZ mice / Third arch artery / Third pharyngeal pouch / Baroreceptors / Neural crest cells / VEGF / Endothelin-1 / Hoxa3ノックアウトマウス / Cx43-lacZトランスジェニック・マウス / 総頚動脈欠損
Research Abstract

Hoxa3 gene is expressed in the third pharyngeal arch and pouch and is required for development of the third arch artery in addition to the thymus, parathyroid land and carotid body. We statistically analyzed malformations of the carotid artery system in Hoxa3 homozygous mutant mice, in comparison with wild-type and heterozygous littermates. In the Hoxa3 homozygotes, the third arch artery was observed at E 10.5 but degenerated at E 11.5. Therefore the common carotid artery, the derivative of the third arch artery was absent or very short in the null mutants. The tunica media of great arteries derived from the arch arteries is formed by the ectomesenchymal neural crest cells. To assess the cause of the third arch artery regression, the Hoxa3 heterozygous mice were crossed with the connexin43-lacZ transgenic mice in which neural crest cells are specified by β-galactosidase expression. The neural crest cells normally migrated into the third pharyngeal arch and surrounded the arch artery in the null mutants as well as wild types. The expressions of VEGF_<165>, its receptors (tyrosine kinases Flt-1 and Flk-1), endothelin ET-1 and dHand which are responsible for development of embryonic blood vessels or arch arteries, were analyzed in the third arch artery of the E 10.5 Hoxa3 null mutants, in comparison with wild types, by the laser capture microdissection and real-time PCR methods. VEGF_<165> mRNA was almost lost and ET-1 mRNA was markedly reduced in the null mutants. Flk-1 mRNA expression was down-regulated whereas Flt-1 mRNA was up-regulated in the mutants. The Hoxa3 gene may ragulate the pathways of both VEGF and ET-1 systems for the third arch artery development.

Report

(3 results)
  • 2003 Annual Research Report   Final Research Report Summary
  • 2002 Annual Research Report
  • Research Products

    (18 results)

All Other

All Publications (18 results)

  • [Publications] kameda, Y.: "Homeobox gene Hoxa3 is essential for the formation of the carotid body in the mouse embryos."Dev.Biol.. 247. 197-209 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y.: "Carotid body and glomus cells distributed in the wall of the common carotid artery in the bird."Micr.Res.Techn.. 59. 196-206 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y.: "Disruption of the Hoxa3 homeobox gene results in anomalies of the carotid artery system and the arterial baroreceptors."Cell Tissue Res.. 311. 343-352 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y.: "Ultrastructural localization of vimentin immunoreactivity and gene expression in tanycytes and their alterations in hamsters kept under different photoperiods."Cell Tissue Res.. 314. 251-262 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y.: "The role of Hoxa3 gene in parathyroid gland organogenesis of the mouse."J.Histochem.Cytochem.. 52(印刷中). (2004)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y., T.Nishimaki, M.Takeichi, O.Chisaka: "Homeobox gene Hoxa3 is essential for the formation of the carotid body in the mouse embryos."Dev.Biol.. 247(1). 197-209 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y.: "Carotid body and glomus cells distributed in the wall of the common carotid artery in the bird."Micr.Res.Techn.. 59(3). 196-206 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y., N.Watari-Goshima, T.Nishimaki, O.Chisaka: "Disruption of the Hoxa3 homeobox gene results in anomalies of the carotid artery system and the arterial baroreceptors."Cell Tissue Res.. 311(3). 343-352 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y., Y.Arai, T.Nishimaki: "Ultrastructural localization of vimentin immunoreactivity and gene expression in tanycytes and their alterations in hamsters kept under different photoperiods."Cell Tissue Res.. 314(2). 251-262 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y., Y.Arai, T.Nishimaki, O.Chisaka: "The role of Hoxa3 gene in parathyroid gland organogenesis of the mouse."J.Histochem.Cytochem.. 52(in press). (2004)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kameda, Y.: "Homeobox gene Hoxa3 is essential for the formation of the carotid body in the mouse embryos."Dev.Biol.. 247・1. 197-209 (2002)

    • Related Report
      2003 Annual Research Report
  • [Publications] Kameda, Y.: "Carotid body and glomus cells distributed in the wall of the common carotid artery in the bird."Micr.Res.Techn.. 59・3. 196-206 (2002)

    • Related Report
      2003 Annual Research Report
  • [Publications] Kameda, Y.: "Disruption of the Hoxa3 homeobox gene results in anomalies of the carotid artery system and the arterial baroreceptors."Cell Tissue Res.. 311・3. 343-352 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Kameda, Y.: "Ultrastructural localization of vimentin immunoreactivity and gene expression in tanycytes and their alterations in hamsters kept under different photoperiods."Cell Tissue Res.. 314・2. 251-262 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Kameda, Y.: "The role of Hoxa3 gene in parathyroid gland organogenesis of the mouse."J.Histochem.Cytochem.. 52(in press). (2004)

    • Related Report
      2003 Annual Research Report
  • [Publications] Yoko Kameda: "Homeobox gene Hoxa3 is essential for the formation of the carotid body in the mouse embryos"Dev. Biol.. 247. 197-209 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Yoko Kameda: "Carotid body and glomus cells distributed in the wall of the common carotid artery in the bird"Micr. Res. Techn.. 59. 196-206 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Yoko Kameda: "Disruption of the Hoxa3 homeobox gene results in anomalies of the carotid artery system"Cell Tissue Res.. (in press). (2003)

    • Related Report
      2002 Annual Research Report

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Published: 2002-04-01   Modified: 2016-04-21  

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