Moore P L, Bank H L, Brissie N T, Spicer S S
J Cell Biol. 1978 Jan;76(1):158-74. doi: 10.1083/jcb.76.1.158.
The changes in membrane structure of rabbit polymorphonuclear (PMN) leukocytes during bacterial phagocytosis was investigated with scanning electron microscope (SEM), thin-section, and freeze-fracture techniques. SEM observations of bacterial attachment sites showed the involvement of limited areas of PMN membrane surface (0.01-0.25mum(2)). Frequently, these areas of attachment were located on membrane extensions. The membrane extensions were present before, during, and after the engulfment of bacteria, but were diminished in size after bacterial engulfment. In general, the results obtained with SEM and thin-section techniques aided in the interpretation of the three-dimensional freeze-fracture replicas. Freeze-fracture results revealed the PMN leukocytes had two fracture faces as determined by the relative density of intramembranous particles (IMP). Membranous extensions of the plasma membrane, lysosomes, and phagocytic vacuoles contained IMP's with a distribution and density similar to those of the plasma membrane. During phagocytosis, IMPs within the plasma membrane did not undergo a massive aggregation. In fact, structural changes within the membranes were infrequent and localized to regions such as the attachment sites of bacteria, the fusion sites on the plasma membrane, and small scale changes in the phagocytic vacuole membrane during membrane fusion. During the formation of the phagocytic vacuole, the IMPs of the plasma membrane appeared to move in with the lipid bilayer while maintaining a distribution and density of IMPs similar to those of the plasma membranes. Occasionally, IMPs were aligned to linear arrays within phagocytic vacuole membranes. This alignment might be due to an interaction with linearly arranged motile structures on the side of the phagocytic vacuole membranes. IMP-free regions were observed after fusion of lysosomes with the phagocytic vacuoles or plasma membrane. These IMP-free areas probably represent sites where membrane fusion occurred between lysosomal membrane and phagocytic vacuole membrane or plasma membrane. Highly symmetrical patterns of IMPs were not observed during lysosomal membrane fusion.
采用扫描电子显微镜(SEM)、超薄切片和冷冻蚀刻技术,研究了兔多形核(PMN)白细胞在细菌吞噬过程中膜结构的变化。对细菌附着部位的SEM观察显示,PMN膜表面有限区域(0.01 - 0.25μm²)参与其中。这些附着区域通常位于膜的延伸部分。膜延伸部分在细菌吞噬之前、期间和之后均存在,但在细菌吞噬后尺寸减小。总体而言,SEM和超薄切片技术获得的结果有助于解释三维冷冻蚀刻复制品。冷冻蚀刻结果显示,根据膜内颗粒(IMP)的相对密度,PMN白细胞有两个断裂面。质膜、溶酶体和吞噬泡的膜延伸部分含有分布和密度与质膜相似的IMP。在吞噬过程中,质膜内的IMP没有发生大量聚集。事实上,膜内的结构变化很少见,且局限于细菌附着部位、质膜融合部位以及吞噬泡膜在膜融合过程中的小规模变化等区域。在吞噬泡形成过程中,质膜的IMP似乎随着脂质双层一起移动,同时保持与质膜相似的IMP分布和密度。偶尔地,IMP在吞噬泡膜内排列成线性阵列。这种排列可能是由于与吞噬泡膜一侧线性排列的运动结构相互作用所致。溶酶体与吞噬泡或质膜融合后观察到无IMP区域。这些无IMP区域可能代表溶酶体膜与吞噬泡膜或质膜之间发生膜融合的部位。在溶酶体膜融合过程中未观察到高度对称的IMP模式。