ヒト皮膚における細胞膜骨格蛋白質の存在と分布 Presence and Localization of Proteins Immunologically Related to Membrane Skeletal Proteins in Human Skin.

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著者

    • 清水, 忠道 シミズ, タダミチ

書誌事項

タイトル

ヒト皮膚における細胞膜骨格蛋白質の存在と分布

タイトル別名

Presence and Localization of Proteins Immunologically Related to Membrane Skeletal Proteins in Human Skin.

著者名

清水, 忠道

著者別名

シミズ, タダミチ

学位授与大学

北海道大学

取得学位

博士 (医学)

学位授与番号

乙第4172号

学位授与年月日

1992-12-25

注記・抄録

博士論文

Recent biochemical studies have shown that spectrin, protein 4.1, and actin form a skeletal protein network that underlines the inner surface of the erythrocyte membrane. The skeleton is a flexible structure that appears to be important in maintaining the shape and mechanical properties of the erythrocyte. Recent studies indicate that immunoanalogues of erythrocyte membrane skeletal proteins and ankyrin (protein 2.1) have been found in a wide variety of non-erythroid tissues. In the present study, in order to examine if human skin contains membrane skeletal proteins. immunochemical analysis was utilized using antibodies against anti-spectrin, anti-β-fodrin (non-erythroid spectrin), anti-protein 4.1 and anti-ankyrin antibodies. Immunoblot analysis of human epidermis with anti-spectrin and anti-β-fodrin antibodies revealed that human epidermis contains 240 kDa and 235 kDa spectrin-like proteins, which might be identical to brain fodrin. Human epidermis also contains 4.1-like proteins of 80 kDa and 78 kDa that cross react with anti-protein 4.1 antibodies, and contains ankyrin-like proteins of 210 kDa that cross react with anti-ankyrin antibodies. Analysis with immunofluorescence microscopy revealed that these antibodies reacted along the plasma membranes of human epidermal keratinocytes, eccrine sweat gland cells and sweat ductal cells. These results suggest that a membrane skeletal protein lattice might exist in these cells. Cultured human epidermal keratinocyte in the low Ca2 medium (0.15 mM) showed that immunoreactive form of protein 4.1 and actin were present diffusely in the cytoplasm. When the cells were cultured with standardized Ca2 medium (1.85 mM), protein 4.1 and actin were observed linearly along the cell margin and in the cytoplasm. Similar patterns of distribution were observed when anti - β – fodrin antibody was used. Movement of membrane skeletal proteins from cytosol to the membrane suggest that these proteins or membrane skeletal lattice might play an important role in the formation of intercellular junctions.

Hokkaido University (北海道大学). 博士(医学)

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各種コード

  • NII論文ID(NAID)
    500000092734
  • NII著者ID(NRID)
    • 8000000092960
  • DOI(NDL)
  • 本文言語コード
    • jpn
  • NDL書誌ID
    • 000000257048
  • データ提供元
    • 機関リポジトリ
    • NDL-OPAC
    • NDLデジタルコレクション
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