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Histogenesis of malignant fibrous histiocytoma (MFH), with a particular reference to the relationship with mesenchymal differentiation

Research Project

Project/Area Number 09660324
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Basic veterinary science/Basic zootechnical science
Research InstitutionOSAKA PREFECTURE UNIVERSITY

Principal Investigator

KUWAMURA Mitsuru  College of Agriculture, Research Assistant, 農学部, 助手 (20244668)

Co-Investigator(Kenkyū-buntansha) KANNAN Yukiko  College of Agriculture, Research Assistant, 農学部, 助手 (80264810)
TAMATE Jyoji  College of Agriculture, Assistant Professor, 農学部, 講師 (50150115)
Project Period (FY) 1997 – 1999
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥3,300,000 (Direct Cost: ¥3,300,000)
Fiscal Year 1999: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1998: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1997: ¥1,600,000 (Direct Cost: ¥1,600,000)
Keywordsmalignant fibrous histiocytoma / mesenchymal primitive cell / multipotential / rat experimental model / monoclonal antibody / mesenchymal differentiation / 間葉系細胞分化様式
Research Abstract

Malignant fibrous histiocytoma (MFH) consists of primitive cells with potential differentiation towards various mesenchymla cells, depending on environmental conditions. In this project, in order to clarify the relationship between MFH cells and other mesenchymal cells, we compared cell characteristics by using some mesenchymal cell lines established by us. Further, we examined the distribution of positive cells against monoclonal antibodies produced by using rat MFH cell line as the immunogen.
1. LPS was added to cultures of MT-9 (rat MFH cell line) and HS-P (rat histiocytic sarcoma-derived cell line), and we examined their nature. Under LPS addition, HS-P increased TNF-α production and enhanced their macrophage-like phenotypes (ED1- and ED2-positive cells). In contrast, there were no such changes in MT-9.
2. Under TGF-β addition, HS-P decreased macrophage-like phenotypes, but MT-9 did not. Based on findings shown above, histiocytic cells constituting MFH differ from true macrophages.
3. We succeeded in generation of rat MFH-specific monoclonal antibodies (A3, B9) by using rat MFH cell line (MT-8) as the immunogen. A3 reacted specifically to primitive mesenchymal cells among organs in the embryogenesis, and B9 labeled cytoplamic lysozyme of macrophages. These findings indicated that MFH cells share a common antigenicity with primitive mesenchymal cells, and have features similar to macrophages/histiocytes.
4. In conclusion, MFH is composed of so-called fibrohistiocytes, and thus we propose the alternative term of undifferentiated mesenchymal sarcoma to the MFH.

Report

(4 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report
  • 1997 Annual Research Report
  • Research Products

    (18 results)

All Other

All Publications (18 results)

  • [Publications] Yamate, J.: "Maacrophage poplations and apoptotic cells in the liver before sponataneous hepatitis in Long-Evans Cinnamon(LEC)rats"Journal of Comparative Pathology. 120. 333-346 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Kumagai, D.: "Distribution of cells labelled by a monoclonal antibody(A3) against a cloned cell line from a rat malignant fibrous histiocytoma"Journal of Comparative Pathology. (in press). (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Yamate J., et al.: "Macrophage populations and apoptotic cells in the liver before spontaneous hepatitis in Long-Evans Cinnamon (LEC) rats."Journal of Comparative Pathology. 120. 333-346 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Kumagai D., et al.: "Distribution of cells labelled by a monoclonal antibody (A3) against a cloned cell line from a rat malignant fibrous histiocytoma."Journal of Comparative Pathology. (in press). (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Yamate,J.: "Macrophage populations and apoptotic cells in the liver before spontaneous hepatitis in Long-Evans Cinnamon(LEC)rats"Journal of Comparative Pathology. 120. 333-346 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Kumagai,D.: "Distribution of cells labelled by a monoclonal antibody(A3) against a cloned cell line from a rat malignant fibrous histiocytoma"Journal of Comparative Pathology. (in press). (2000)

    • Related Report
      1999 Annual Research Report
  • [Publications] Yamate,J.: "Characteristics of rat fibrosarcoma-derived transplantable tumor line(SS)and cultured cell lines(SS-P and SS-A3-1),showing myofibroblastic and histiocytic phenotypes." Virchows Archive. 431. 431-440 (1997)

    • Related Report
      1998 Annual Research Report
  • [Publications] Tsunenari,I.: "Angioarchitecture of tumors induced by two different cloned cell lines established from a transplantable rat malignant fibrous histiocytoma." Scanning Microscopy. 11. 473-482 (1997)

    • Related Report
      1998 Annual Research Report
  • [Publications] Kuwamura,M.: "Urinary bladder rhabdomyosarcoma(sarcoma botryoides)in a young Newfaundland dog." Journal of Veterinary Medical Science. 60. 619-621 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Yamate,J.: "Lysozyme-containing renal hyaline droplets in rats with a transplantable fibrosarcoma(SS)." Toxicologic Pathology. 26. 699-703 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Yamate,J.: "Influence of progesterone and oestrogen on tumour growth and morphology of a transplantable rat uterine smooth muscle tumour(SMT-Y)." Journal of Comparative Pathology. 119. 443-457 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Yamate,J.: "The underlying roles of macrophage populations in myocardial fibrosis." Biomedical Reviews. (in press). (1999)

    • Related Report
      1998 Annual Research Report
  • [Publications] Yamate J,et al.: "Morphological characteristics of a transplantable histiocytic sarcoma (HS-J) in F344 rats and appearance of renal tubular hyaline droplets in HS-J-bearing rats" Journal of Comparative Pathology. 116. 73-86 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Yamate J,et al.: "Phenotypic changes in lipopolysaccharide-treated cloned cells derived from transplantable rat malignant fibrous histiocytoma" Journal of Veterinary Medical Science. 58. 1017-1020 (1996)

    • Related Report
      1997 Annual Research Report
  • [Publications] Yamate J,et al.: "Phenotypic modulation in cisplatin-resistant cloned cells derived from tansplantable rat malignant fibrous histiocytoma" Pathology International. 46. 557-567 (1996)

    • Related Report
      1997 Annual Research Report
  • [Publications] Yamate J,et al.: "Heterogeneity in the origin and immunophenotypes of "histiocytic" cells in transplantable rat malignant fibrous histiocytoma" Journal of Veterinary Medical Science. 58. 603-609 (1996)

    • Related Report
      1997 Annual Research Report
  • [Publications] Tsujino K,et al.: "Establishment and characterization of cell lines derived from a transplantable rat malignant meningioma : morphological heterogeneity and production of nerve growth factor" Acta Neuropathologica. 93. 461-470 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Yamate J,et al.: "Characteristics of a rat fibrosarcoma-derived transplantable tumour line (SS) and cultured cell lines (SS-P and SS-A3-1) showing myofibroblastic and histiocytic phenotypes" Virchows Archives. 431. 431-440 (1997)

    • Related Report
      1997 Annual Research Report

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Published: 1997-04-01   Modified: 2016-04-21  

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