Harwick H J, Barajas L, Montgomerie J Z, Kalmanson G M, Guze L B
Infect Immun. 1972 Jun;5(6):976-81. doi: 10.1128/iai.5.6.976-981.1972.
Little data are available regarding L-form phagocyte interactions. Due to difficulty with more conventional methods, a serum-free technique of surface phagocytosis employing cellulose ester micropore filters, fluorochrome staining, and reflecting fluorescence microscopy was developed. Intracellular localization of L-frms was confirmed by electron microscopy. In timed experiments, phagocytosis of a group D Streptococcus (ATCC 23241) and its L-form (T53I) were maximal at 30 min, although the bacteria were consistently better phagocyted. Phagocytosis of an Escherichia coli (strain Yale) and its L-form was also demonstrated with the same technique. The lesser phagocytosis of L-forms may be related to their lower chemotactic activity.
关于L型与吞噬细胞相互作用的数据很少。由于传统方法存在困难,因此开发了一种无血清的表面吞噬技术,该技术采用纤维素酯微孔滤膜、荧光染料染色和反射荧光显微镜。通过电子显微镜确认了L型菌在细胞内的定位。在定时实验中,D组链球菌(ATCC 23241)及其L型菌(T53I)的吞噬作用在30分钟时达到最大值,不过细菌始终更容易被吞噬。同样的技术也证实了大肠杆菌(耶鲁菌株)及其L型菌的吞噬作用。L型菌吞噬作用较弱可能与其较低的趋化活性有关。