求帮忙下这篇文献

zszhao

http://www.nature.com/ni/journal/v13/n6/full/ni.2301.html顺便下一下补充的pdf
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ipsvirus

zszhao 发表于 2015-11-19 13:09
, l( w6 ^7 C  n# P，谢谢啦

已发，请查收

zszhao

marine0425030 发表于 2015-11-18 09:34
( g* m% C2 u1 xTespa1 is involved in late thymocyte development through the regulation of TCR-mediated signaling
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未来的老板

zszhao

ipsvirus 发表于 2015-11-18 11:04
2 H5 i5 p. u5 H- D  N/ ^7 d文件有点大，留个邮箱吧，我发你

7 U" u) W, t7 j' W6 u8 C0 X& R1455710563@qq.com，谢谢啦

ipsvirus

文件有点大，留个邮箱吧，我发你

marine0425030

Tespa1 is involved in late thymocyte development through the regulation of TCR-mediated signaling

' _% q2 m2 ?. E' c. b. u Di Wang,        Mingzhu Zheng,        Lei Lei,        Jian Ji,        Yunliang Yao,        Yuanjun Qiu,        Lie Ma,        Jun Lou,        Chuan Ouyang,        Xue Zhang,        Yuewei He,        Jun Chi,        Lie Wang,        Ying Kuang,        Jianli Wang,        Xuetao Cao        & Linrong Lu
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- W( _$ q+ |" i# M$ nSignaling via the T cell antigen receptor (TCR) during the CD4+CD8+ double-positive developmental stage determines thymocyte selection and lineage commitment. Here we describe a previously uncharacterized T cell–expressed protein, Tespa1, with critical functions during the positive selection of thymocytes. Tespa1−/− mice had fewer mature thymic CD4+ and CD8+ T cells, which reflected impaired thymocyte development. Tespa1 associated with the TCR signaling components PLC-γ1 and Grb2, and Tespa1 deficiency resulted in attenuated TCR signaling, as reflected by defective activation of the Erk–AP-1 and Ca2+-NFAT pathways. Our findings demonstrate that Tespa1 is a component of the TCR signalosome and is essential for T cell selection and maturation through the regulation of TCR signaling during T cell development.
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鲁教授又出好文章了。