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肺炎链球菌侵袭人II型肺细胞过程中的钙信号事件。

Calcium signaling events in Streptococcus pneumoniae invasion of human type II pneumocytes.

作者信息

Xu Bang-lao, Yin Yi-bing

机构信息

Department of Clinical Laboratory, First Municipal Hospital of Guangzhou, Guangzhou 510180, China.

出版信息

Di Yi Jun Yi Da Xue Xue Bao. 2004 Feb;24(2):168-71, 176.

Abstract

OBJECTIVE

To study whether Streptococcus pneumoniae (S.pn) can provoke filamentous actin (F-actin) rearrangements in vitro through calcium signaling pathways in type II pneumocytes(A549 cells), resulting in S.pn invasion of the cells.

METHOD

After FITC-phalloidin labeling of F-actin, F-actin rearrangements were observed by S.pn adhesion to type pneumocyte A549 cells. S.pn invasion of A549 cells was determined by pretreating A549 cells with cytochalasin D. To investigate whether F-actin rearrangements could be blocked by Ca2+ inhibitors, A549 cells were pretreated with Ca2+ inhibitors dantrolene, and loaded in Fura-2/AM probe to determine the concentration of cytosolic free calcium by S.pn adhesion to A549 cells after 30, 60, and 90 min respectively.

RESULTS

Intact S.pn can promote F-actin rearrangements. Cytochalasin D was able to prevent S.pn invasion of A549 cells. No invasion of A549 cell can be determined at 0.25 microg/ml of cytochalasin D. One subset of the inhibitors of Ca2+ signal transduction molecules blocked F-actin rearrangements dose-dependently, and S.pn adhesion of A549 cells for 30, 60, and 90 min increased cytosolic free calcium, reaching 487.5+/-38.1 , 548.2+/-35.6 and 557.2+/-47.5 nmol/L, respectively. They were higher than of the control group.

CONCLUSION

S.pn can provoke F-actin rearrangements through Ca2+ signaling pathways, which further leads to S.pn invasion of A549 cells.

摘要

目的

研究肺炎链球菌(S.pn)是否能通过Ⅱ型肺上皮细胞(A549细胞)中的钙信号通路在体外引发丝状肌动蛋白(F-肌动蛋白)重排,从而导致S.pn侵袭细胞。

方法

用异硫氰酸荧光素(FITC)-鬼笔环肽标记F-肌动蛋白后,通过观察S.pn黏附于肺上皮细胞A549细胞来观察F-肌动蛋白重排情况。用细胞松弛素D预处理A549细胞来测定S.pn对A549细胞的侵袭。为研究F-肌动蛋白重排是否能被钙离子抑制剂阻断,用钙离子抑制剂丹曲林预处理A549细胞,并加载Fura-2/AM探针,分别在30、60和90分钟后通过S.pn黏附于A549细胞来测定胞质游离钙浓度。

结果

完整的S.pn能促进F-肌动蛋白重排。细胞松弛素D能够阻止S.pn对A549细胞的侵袭。在细胞松弛素D浓度为0.25微克/毫升时未检测到A549细胞被侵袭。钙离子信号转导分子抑制剂的一个亚组能剂量依赖性地阻断F-肌动蛋白重排,且S.pn黏附A549细胞30、60和90分钟后胞质游离钙增加,分别达到487.5±38.1、548.2±35.6和557.2±47.5纳摩尔/升。它们高于对照组。

结论

S.pn可通过钙信号通路引发F-肌动蛋白重排,进而导致S.pn侵袭A549细胞。

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