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Human natural helper cells and its involvement in diseases

Human natural helper cells and its involvement in diseases
人类天然辅助细胞及其与疾病的关系
批准号:
23390086
负责人:
YAMADA TAKETO
金额:
$12.65万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011-04-01 至 2014-03-31

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中文摘要
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英文摘要
Pathophysiological examinations of human innate immunology-related natural helper (NH) cells in fat-associated lymphoid cluster (LALC) were done using autopsy cases. FALCs in adipose tissues of total body were analyzed anatomically and histologically, consequently FALC was dominantly located in mesentery and NH cells were most frequent in mesentery as compared to omentum, fat capsule of kidney, genitalia, and retroperitoneum. Hunan NH cells prepared from human mesentery had the same patterns of gene expressions and similar kinds of cytokine production to murine NH cells. Human NH cells labeled with CSFE were transplanted in NOG mice. As a result human NH cells lodged in murine adipose tissues and produced human IL-5 and IL-13 constitutively. The area of FALC and NH cell number was decreased in mesentery of cases with diabetes mellitus and metabolic syndrome as compared to control cases.
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The Pathogenesis of pulmonary alveolar proteinosis in PI3K deficient mice
PI3K缺陷小鼠肺泡蛋白沉积症的发病机制
DOI: --
发表时间: 2013
期刊:
影响因子: --
作者: [Nagai S, Yoshizawa A, Baba Y, Yamada T, Nishimura T, Koyasu S]
通讯作者: Koyasu S
Change in beta cell and alpha cell mass in Japanese obese individuals.
日本肥胖者β细胞和α细胞质量的变化。
DOI: --
发表时间: 2012
期刊:
影响因子: --
作者: [Furuhashi T, Saito C, Torii K, Nishida E, Yamazaki S, Morita A, 鏡雅代など, Kou K]
通讯作者: Kou K
A mimic of viral dsRNA triggers fulminant type 1 diabetes-like syndrome in regulatory T cell-deficient autoimmune diabetic mouse
病毒 dsRNA 的模拟物在调节性 T 细胞缺陷的自身免疫糖尿病小鼠中引发暴发性 1 型糖尿病样综合征
DOI: --
发表时间: 2011
期刊: Journal of Immunology
影响因子: 4.4
作者: [Tada A, Shimada A, Yamada T, Oikawa Y, Yamada Y, Okubo Y, Irie J, Bluestone JA, Itoh H]
通讯作者: Itoh H
Impairment of cell growth by down regulation of NCAP2 gene transcription mediated with nuclear transported CD26 using humanized anti-CD26 monoclonal antibody.
使用人源化抗 CD26 单克隆抗体,通过核转运 CD26 介导的 NCAP2 基因转录下调来损害细胞生长。
DOI: --
发表时间: 2012
期刊:
影响因子: --
作者: [山崎小百合, 森田明理, 鏡雅代, Yamada T]
通讯作者: Yamada T
13
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