The involvement of chemokines in thymic atrophy and its application to forensic practices
Project/Area Number |
16H07133
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Research Category |
Grant-in-Aid for Research Activity Start-up
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Allocation Type | Single-year Grants |
Research Field |
Legal medicine
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Research Institution | Wakayama Medical University |
Principal Investigator |
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Project Period (FY) |
2016-08-26 – 2018-03-31
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Project Status |
Completed (Fiscal Year 2017)
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Budget Amount *help |
¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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Keywords | 胸腺萎縮 / 児童虐待 / ストレス / サイトカイン / ケモカイン / 虐待 / 胸腺 / CCR5 / CCR5リガンド / 法医病理学 |
Outline of Final Research Achievements |
We examined the pathophysiological roles of CCR5 in stress-induced thymic atrophy. C57BL/6 (WT) and Ccr5 KO mice were immobilized individually in well-ventilated restrainers for 1 hour daily, and this procedure were repeated the following 2 days. When WT mice were restrained, the thymuses significantly involuted and their weight decreased to 25% of unrestrained thymus weight. However, in Ccr5 KO mice treated with the same manner, the decrease of thymus weight was significantly suppressed. In the next series, restrain stress significantly induced the apoptosis in the thymic cells of WT mice. On the contrary, the absence of CCR5 significantly suppressed apoptosis of thymic cells. These observations implied that the absence of CCR5 resisted stress-induced thymic atrophy. Thus, CCR5-mdiated signals would promote thymic involution induced by restrain stress. From the forensic aspects, CCR5 would be a key molecule for diagnosing abuse in infants and children.
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Report
(3 results)
Research Products
(4 results)
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[Journal Article] Exaggerated arsenic nephrotoxicity in female mice through estrogen-dependent impairments in the autophagic flux.2016
Author(s)
Kimura A, Ishida Y, Nosaka M, Kuninaka Y, Hama M, Kawaguchi T, Sakamoto S, Shinozaki K, Iwahashi Y, Takayasu T, Kondo T.
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Journal Title
Toxicology.
Volume: 339
Pages: 9-18
DOI
Related Report
Peer Reviewed
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