Norkin L C
Department of Microbiology, University of Massachusetts, 203 Morrill Science Center IVN, Amherst, MA 01003-5720, USA.
Adv Drug Deliv Rev. 2001 Jul 28;49(3):301-15. doi: 10.1016/s0169-409x(01)00143-0.
A variety of microbial pathogens, including viruses, intracellular bacteria, and prions, as well as certain secreted bacterial toxins, can now be added to the list of ligands that enter cells via caveolae or caveolae-like membrane domains. In general, the caveolae-mediated entry pathway results in transport of these microbes and toxins to intracellular destinations that are different from that of cargo entering by other means. As a result, the caveolae-mediated entry pathway can profoundly affect the host cell-pathogen interaction long after entry has occurred. Furthermore, some microbes such as SV40 that enter via cavolae will be valuable as probes to analyze certain poorly understood intracellular trafficking pathways, such as retrograde transport to the ER. Also, viruses that enter via caveolae may have unique potential as gene and drug delivery vectors. In addition, some extracellular microbial pathogens, such as Pneumocystis carinii, may also interact with host cells via caveolae. Finally, caveolae may play a role in host immune defense mechanisms.
多种微生物病原体,包括病毒、细胞内细菌和朊病毒,以及某些分泌性细菌毒素,现在都可以添加到通过小窝或类小窝膜结构域进入细胞的配体列表中。一般来说,小窝介导的进入途径会导致这些微生物和毒素被转运到细胞内的目的地,这些目的地与通过其他方式进入的货物不同。因此,小窝介导的进入途径在进入发生很久之后仍能深刻影响宿主细胞与病原体的相互作用。此外,一些通过小窝进入的微生物,如SV40,将作为分析某些了解较少的细胞内运输途径(如逆行运输到内质网)的探针具有重要价值。同样,通过小窝进入的病毒作为基因和药物递送载体可能具有独特的潜力。此外,一些细胞外微生物病原体,如卡氏肺孢子虫,也可能通过小窝与宿主细胞相互作用。最后,小窝可能在宿主免疫防御机制中发挥作用。