1991 Fiscal Year Final Research Report Summary
Changes in the Cellular Elements of the Connective Tissues During Amphibian Metamorphosis
Project/Area Number |
02640588
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Research Category |
Grant-in-Aid for General Scientific Research (C)
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Allocation Type | Single-year Grants |
Research Field |
動物形態・分類学
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Research Institution | Tsurumi University |
Principal Investigator |
SASAKI Fumie Tsurumi University. Dept. of Biology Professor, 教養部, 教授 (30064372)
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Co-Investigator(Kenkyū-buntansha) |
HIRATA Junko Tsurumi University. Dept. of Biology Assistant, 教養学部, 助手 (10228786)
NISHIKAWA Sumio Tsurumi University. Dept. of Biology Assistant, 教養学部, 助手 (60097277)
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Project Period (FY) |
1990 – 1991
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Keywords | Amphibia / Connective tissue / Fibroblast / Extracellular matrix / Collagen / Proteoglycan / Immunohistochemistry |
Research Abstract |
Morphological and biochemical changes of the connective tissues in amphibian larvae during developmental stages are investigated using immunoflourescence markers and electron microscopy, and compared with the extracellular matrix (ECM) of Anura and Urodela. In these experiments, the ECM component of the connective tissues in frozen sections of these larvae was stained with antibodies. The antibodies used were as follows : anti-PG-H to the notochordal proteoglycan (PG) of Rana catesbeiana, anti-keratan sulfate PG (KS), anti-chondroitin 4 sulfate PG (C4S), anti-chondroitin 6 sulfate PG (C6S), anti-Type I collagen, anti-Type III collagen, anti-Type IV collagen, and anti-Type VII collagen. In Cynops pyrrhogaster, Type I and Type III collagen antibodies stained the skin and myoseptum, and the peripheral regions containing connective tissues and cartilages. However, Type III collagen antibody was not observed in Rana japonica. Anti-KS especially stained notochord in the early stage of larvae. Positive staining with anti-PG-H of the peripheral regions of the notochordalsheath and ganglia persisted through the late metamorphosis. Using HPLC, we were able to separate C4S from notochordal PG of Rana catesbeiana for the first time. We are now planning to analyze the core proteins in the PG structure, and apply the results to immunocytochemical studies. The PG distribution and pattern of occurrence may provide us with some clues to help dispel the myths surrounding the evolutional process of these species.
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