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Analysis of β cell differentiation in diabetic pancreas induced by betacellulin with special reference to the role of Pax family gene

Research Project

Project/Area Number 11671087
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Endocrinology
Research InstitutionOsaka University

Principal Investigator

MIYAGAWA Jun-ichiro  Osaka University Graduate School of Medicine, Lecturer, 医学系研究科, 講師 (00127721)

Co-Investigator(Kenkyū-buntansha) SASADA Reiko  Takeda Chemical Industries, Researcher, 医薬開拓研究本部・開拓第二研究所, 主任研究員
HIGASHIYAMA Shigeki  Osaka University Medical School, Associate Professor, 医学部, 助教授 (60202272)
YAMAMOTO Koii  Osaka University Hospital, Assistant Professor, 医学部・附属病院, 助手 (60304060)
北島 孝一  大阪大学, 医学系研究科, 助手 (00314310)
花房 俊昭  大阪大学, 医学系研究科, 講師 (60164886)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2000: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1999: ¥2,500,000 (Direct Cost: ¥2,500,000)
Keywordsβcell / Diabetes mellitus / Regeneration / Differentiation / Betacellulin / Transcription factor / Pax6 / 増殖因子 / Paxファミリー
Research Abstract

In the development of endocrine pancreas, various transcription factors that regulate the expression of growth and differentiation factors are involved. Among them, Pax family is known to have important role in the final differentiation of insulin-secreting β cells. On the other hand, little is known in the mechanism of neogenesis which occurs in the β cell depleted diabetic pancreas. We thus studied the process of β cell neogenesis with special reference to the expression of transcription factors including Pax family in pancreas of glucose intolerant mice induced by selective alloxan perfusion. We also tried to clarify the role of Pax 6 and 4 using dominant negative form of these genes introduced in AR42J cells. ICCs(Islet-like cell clusters) were observed closely associated with duct cell lining, and immunohistochemical analysis revealed that several kinds of transcription factors including PDX-1, Islet1, Nkx2.2 and Pax6 were expressed in some of duct cells and Icc cells, suggesting that Pax6 is involved in the β cell neogenesis in diabetic pancreas and the process of this type of regeneration (neogenesis) was similar to that of fetal endocrine cell development . However, Pax4 which is important for the final differentiation of β cells during development was undetectable level. Treatment with betacellulin , one of the growth factor of EGF family and is known to induce differentiation of AR42J cells into insulin-producing endocrine cells, increased the number of ICCs and ameliorate the glucose intolerance. To clarify the role of Pax4 and Pax6 in the β cell differentiation, we tried to make stable transformants of dominant negative form of these genes in AR42J cells, but this was difficult, and we could not analyze the roles of two Pax genes in β cell differentiation using in vitro experimental system.

Report

(3 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • Research Products

    (24 results)

All Other

All Publications (24 results)

  • [Publications] Yamamoto K.,Miyagawa J.,Waguri M., et al.: "Recombinant human betacellulin promotes neogenesis of β-cells and ameliorates glucose intolerance in mice with diabetes induced by selective alloxan perfusion"Diabetes. 49. 2021-2027 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Imagawa A.,Hanafusa T.,Miyagawa J., et al.: "A proposal of three distinct subtypes of type 1 diabetes mellitus based on clinical and pathological evidence."Ann Med. 32. 527-531 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yang Q,,Yamagata K.,Yamamoto K.,Cao Y.,Miyagawa J., et al.: "R127W-HNF-4α is a loss of function mutation but not a rare polymorphism and causes Type II diabetes in a Japanese family with MODY1."Diabetologia. 43. 520-524 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 宮川潤一郎: "膵β細胞の再生能"Medical Practice. 17・1. 106-107 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 今川彰久,森脇信,花房俊昭,宮川潤一郎: "1型糖尿病膵の細胞生物学と病態"細胞. 32・12. 448-451 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 山本浩司,宮川潤一郎: "膵β細胞の再生促進療法"Molecular Medicine. 38・1. 62-67 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yamamoto K., Miyagawa J., Waguri M., Sasada R., Igarashi K., Li M., Nammo T., Moriwaki M., Imagawa A., Yamagata K., Nakajima H., Namba M., Hanafusa T., Matsuzawa Y.: "Recombinant human betacellulin promotes neogenesis of β-Cells and ameliorates glucose intolerance in mice with diabetes induced by selective alloxan perfusion."Diabetes. 49. 2021-2027 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Imagawa A., Hanafusa T., Miyagawa J., Matsuzawa Y.: "A proposal of three distinct subtypes of type 1 diabetes mellitus based on clinical and pathological evidence."Ann Med. 32. 527-531 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yang Q., Yamagata K., Yamamoto K., Cao Y., Miyagawa J., Fukamizu A., Hanafusa T., Matsuzawa Y.: "P127W-HNF-4α is a loss of function mutation but not a rare polymorphism and causes Type II diabetes in a Japanese family with MODY1."Diabetologia. 43. 520-524 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Zhu Q., Yamagata K, Yu L., Tomura H., Yamada S., Yang Q., Yoshiuchi I., Sumi S., Miyagawa J., Takeda J., Hanafusa T., Matsuzawa Y.: "Identification of missense mutations in the hepatocyte nuclear factor-3β gene in Japanese subjects with late-onset type II diabetes mellitus."Diabetologia. 43. 1197-1200 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tokumaru S., Higashiyama S., Endo T., Nakagawa T., Miyagawa J., Hanakawa Y., Ohmoto H., Yoshino K., Shirakata Y., Matsuzawa Y., Hashimoto K., Taniguchi N.: "Ectodomain shedding of epidermal growth factor receptor ligands is required for keratinocyte migration in cutaneous wound healing."J Cell Biol. 151 (2). 209-219 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Iizuka K., Nakajima H., Ono A., Okita K., Miyazaki J., Miyagawa J., Namba M., Hanafusa T., Matsuzawa Y.: "Stable overexpression of the glucose-6- phosphatase catalytic subunit attenuates glucose sensitivity of insulin secretion from a mouse pancreatic beta cell line."J Endocrinol. 164. 307-314 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Sawada-Hase N., Kiyohara T., Miyagawa J., Ueyama H., Nishibayashi H., Murayama Y., Kashihara T., Nakahara M., Miyazaki Y., Kanayama S., Nezu R., Shinomura Y., Matsuzawa Y.: "An increased number of CD40 high monocytes discriminate Crohn's disease from ulcerative colitis."Am J Gastroenterol. 95 (6). 1516-1523 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Nishida M., Miyagawa J., Yamashita S., Higashiyama S., Nakata A., Ohuchi N., Tamura R., Yamamori K., Kihara S., Taniguchi N., Matsuzawa Y.: "Localization of CD9, an enhancer protein for proHeparin-binding EGF-like growth factor, in human atherosclerotic plaques -A possible involvement of juxtacrine growth machanism on smooth muscle cell proliferation -."Arterioscler Thromb Vasc Biol. 20. 1236-1243 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Kawasaki A., Matsumura I., Miyagawa Y., Ezoe S., Tanaka H., Terada Y., Tatsuka M., Machii T., Miyazaki H., Furukawa Y., Kanakura Y.: "Downregulation of AIM-1 kinase couples with megakaryocytic polyploidization of human hematopoietic cells."J Cell Bioll. 152 (2). 275-287 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yamamoto K.,Miyagawa J.,Waguri M., et al.: "Recombinant human betacellulin promotes neogenesis of β-cells and ameliorates glucose intolerance in mice with diabetes induced by selective alloxan perfusion"Diabetes. 49. 2021-2027 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Imagawa A.,Hanafusa T.,Miyagawa J., et al.: "A proposal of three distinct subtypes of type 1 diabetes mellitus based on clinical and pathological evidence."Ann Med. 32. 527-531 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Yang Q.,Yamagata K.,Yamamoto K.,Cao Y.,Miyagawa J., et al.: "R127W-HNF-4α is a loss of function mutation but not a rare polymorphism and causes Type II diabetes in a Japanese family with MODY1."Diabetologia. 43. 520-524 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] 宮川潤一郎: "膵β細胞の再生能"Medical Practice. 17・1. 106-107 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] 今川彰久,森脇信,花房俊昭,宮川潤一郎: "1型糖尿病膵の細胞生物学と病態"細胞. 32・12. 448-451 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] 宮川潤一郎,山本浩司: "膵β細胞の再生促進療法"Molecular Medicine. 38・1. 62-67 (2001)

    • Related Report
      2000 Annual Research Report
  • [Publications] J.Miyagawa,T.Hanafusa,R.Sasada et al.: "Immunohistochemical localization of a Betacellulin, a new member of the EGF family, in normal human pancreas and islet tumor cells"Endocrine Journal. 46・6. 755-764 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] 宮川潤一郎,花房俊昭: "膵β細胞再生促進療法の可能性"医学のあゆみ. 188・2. 121-125 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] 宮川潤一郎: "膵β細胞の再生能"Medical Practice. 17・1. 106-107 (2000)

    • Related Report
      1999 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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