| Project/Area Number |
17590170
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
General anatomy (including Histology/Embryology)
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| Research Institution | Wakayama Medical University |
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Principal Investigator |
TSURUO Yoshihiro Wakayama Med Univ, Med Sch, Professor, 医学部, 教授 (90207449)
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| Co-Investigator(Kenkyū-buntansha) |
UEYAMA Takashi Wakayama Med Univ, Med Sch, Associate Professor, 医学部, 助教授 (50264875)
ITO Takao Wakayama Med Univ, Med Sch, Research Associate, 医学部, 助手 (30315931)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,700,000 (Direct Cost: ¥3,700,000)
Fiscal Year 2006: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2005: ¥2,000,000 (Direct Cost: ¥2,000,000)
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| Keywords | lymphoid tissues / steroid / metabolizing enzyme / regulation / immunohistochemistry / rats |
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| Research Abstract |
Concerning the ability of steroid synthesis in the rat abdominal organs, we already reported that the parietal cells in the rat stomach secrete estrogens into the portal vessels. We hypothesized that there is a species difference in the steroid synthesis in the abdominal organs and in mammals including the primates the lymphoid tissues including spleen can synthesize estrogens and the synthesized steroids make some regulations in the lymphoid tissues or through the relation between the lymphoid tissues and the liver. Therefore we examined immunohistochemically the expression of some steroid metabolizing enzymes including aromatase in the lymphoid tissues, which contained thymus, spleen, lymph nodes and Payer's patches of ileum, of rats during postnatal development. We used the following antibodies against aromatase, 5α-reductase type 1, 2, 3α-hydroxysteroid dehydrogenase, 3β-hydroxysteroid dehydrogenase, cholesterol side-chain cleavage enzyme and so on. These steroid metabolizing enzymes were expressed in the lymphocytes, macrophages, dendritic cells, epithelial reticular cells after the early postnatal period onwards. The cellular pattern of the expression was characteristic of each enzyme.
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