首页> 外文期刊>Advances in Experimental Medicine and Biology >The exosporium of B. cereus contains a binding site for gC1qR/p33: implication in spore attachment and/or entry.
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The exosporium of B. cereus contains a binding site for gC1qR/p33: implication in spore attachment and/or entry.

机译:蜡状芽孢杆菌的外孢子含有gC1qR / p33的结合位点:暗示孢子附着和/或进入。

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摘要

B. cereus, is a member of a genus of aerobic, gram-positive, spore-forming rod-like bacilli, which includes the deadly, B. anthracis. Preliminary experiments have shown that gC1qR binds to B. cereus spores that have been attached to microtiter plates. The present studies were therefore undertaken, to examine if cell surface gC1qR plays a role in B. cereus spore attachment and/or entry. Monolayers of human colon carcinoma (Caco-2) and lung cells were grown to confluency on 6 mm coverslips in shell vials with gentle swirling in a shaker incubator. Then, 2 microl of a suspension of strain SB460 B. cereus spores (3x10(8)/ml, in sterile water), were added and incubated (1-4 h; 36 degrees C) in the presence or absence of anti-gC1qR mAb-carbon nanoloops. Examination of these cells by EM revealed that: (1) When B. cereus endospores contacted the apical Caco-2 cell surface, or lung cells, gC1qR was simultaneously detectable, indicating upregulation of the molecule. (2) In areas showing spore contact with the cell surface, gC1qR expression was often adjacent to the spores in association with microvilli (Caco-2 cells) or cytoskeletal projections (lung cells). (3) Furthermore, the exosporia of the activated and germinating spores were often decorated with mAb-nanoloops. These observations were further corroborated by experiments in which B.cereus spores were readily taken up by monocytes and neutrophils, and this uptake was partially inhibited by mAb 60.11, which recognizes the C1q binding site on gC1qR. Taken together, the data suggest a role, for gC1qR at least in the initial stages of spore attachment and/or entry.
机译:蜡状芽孢杆菌是好氧,革兰氏阳性,形成孢子的杆状芽孢杆菌属的成员,其中包括致命的炭疽芽孢杆菌。初步实验表明,gC1qR与已经附着在微量滴定板上的蜡状芽孢杆菌孢子结合。因此,进行了本研究,以检查细胞表面gC1qR是否在蜡状芽孢杆菌的孢子附着和/或进入中起作用。将人结肠癌(Caco-2)和肺细胞的单层细胞在摇瓶培养箱中轻轻旋转的情况下,在小瓶中的6 mm盖玻片上生长至汇合。然后,加入2微升SB460蜡状芽孢杆菌孢子悬浮液(3x10(8)/ ml,在无菌水中),在存在或不存在抗gC1qR的情况下孵育(1-4小时; 36摄氏度) mAb-碳纳米环。 EM对这些细胞的检查表明:(1)当蜡状芽孢杆菌的内生孢子接触顶Caco-2细胞表面或肺细胞时,同时可检测到gC1qR,表明该分子的上调。 (2)在显示孢子与细胞表面接触的区域中,gC1qR表达通常与孢子相邻,并伴有微绒毛(Caco-2细胞)或细胞骨架突起(肺细胞)。 (3)此外,活化和发芽孢子的孢子囊外壁经常用mAb-nanoloops装饰。这些观察结果得到了实验的进一步证实,其中蜡状芽孢杆菌的孢子很容易被单核细胞和中性粒细胞吸收,并且这种吸收被mAb 60.11部分抑制,mAb 60.11识别了gC1qR上的C1q结合位点。总体而言,数据表明至少在孢子附着和/或进入的初始阶段,gC1qR发挥了作用。

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