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纽蛋白、踝蛋白和整合素定位于恶性B淋巴细胞的特定黏附位点。

Vinculin, talin, and integrins are localized at specific adhesion sites of malignant B lymphocytes.

作者信息

Marchisio P C, Bergui L, Corbascio G C, Cremona O, D'Urso N, Schena M, Tesio L, Caligaris-Cappio F

机构信息

Dipartimento di Scienze Biomediche e Oncologia Umana, Università di Torino, Italy.

出版信息

Blood. 1988 Aug;72(2):830-3.

PMID:3135866
Abstract

The microanatomy of the dot-shaped, close-contact sites called podosomes and the mechanism of their formation have been investigated in vitro in the malignant lymphocytes of B chronic lymphocytic leukemia (B-CLL). In this paper the authors demonstrate that in B-CLL podosomes: (1) vinculin, talin, and beta 2 integrin (CD18) rings surround an F-actin core; (2) the beta 1 integrin is localized within the F-actin core; (3) the beta 3 integrin is not present. This distribution and organization of adhesion-related molecules appears to be unique to B-CLL lymphocytes, since it has not been observed in normal B cells. B-CLL adhesion and podosome formation are inhibited by the synthetic peptide GRGDSP that contains the Arg-Gly-Asp (RGD) sequence.

摘要

在体外对B慢性淋巴细胞白血病(B-CLL)恶性淋巴细胞中称为足体的点状紧密接触位点的微观解剖结构及其形成机制进行了研究。在本文中,作者证明,在B-CLL中足体:(1)纽蛋白、踝蛋白和β2整合素(CD18)环围绕着F-肌动蛋白核心;(2)β1整合素定位于F-肌动蛋白核心内;(3)不存在β3整合素。这种黏附相关分子的分布和组织似乎是B-CLL淋巴细胞所特有的,因为在正常B细胞中未观察到。含有精氨酸-甘氨酸-天冬氨酸(RGD)序列的合成肽GRGDSP可抑制B-CLL黏附和足体形成。

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