Knapp P E, Skoff R P, Sprinkle T J
Department of Anatomy and Cell Biology, Wayne State University School of Medicine, Detroit, MI 48201.
J Neurosci Res. 1988 Oct-Dec;21(2-4):249-59. doi: 10.1002/jnr.490210217.
This paper describes the differential expression and localization of myelin components within membrane sheets produced by oligodendrocytes in vitro. In double-labeling experiments using antibodies to the myelin antigens 2',3'-cyclic nucleotide 3'-phosphohydrolase (CNP) and galactocerebroside (GC), the two antigens were coexpressed in at least 95% of oligodendrocytes at all ages examined. A small population of relatively undifferentiated cells expressed one antigen before the other. Within the membrane sheets produced by the cultured cells, CNP and GC are distributed differently. CNP is highly concentrated in cell bodies, in a network of processes extending from the cell body into the sheets, and around the perimeter of the sheets. CNP staining cannot be detected in some areas within the body of the sheet. When present, it is of low intensity. Under our labeling conditions, GC staining is found throughout the membrane sheets, except in the network of veins which are CNP+. GC and myelin basic protein (MBP) staining are seen in similar membrane domains even though GC is a surface component while MBP resides on the cytoplasmic face. Both the timing and localization of CNP immunostaining show that CNP is as early a marker for oligodendrocytes as GC, and support the idea that CNP may play a structural role in the myelin membrane. Double-labeling studies with GC and CNP antibodies also show that the true shape of a cell and the extent of its development are not always revealed by a single antigen. The differential distribution of antigens within membrane sheets illustrates that they contain areas of structural specialization that may reflect the situation in intact myelin.
本文描述了体外少突胶质细胞产生的细胞膜片中髓鞘成分的差异表达和定位。在使用针对髓鞘抗原2',3'-环核苷酸3'-磷酸水解酶(CNP)和半乳糖脑苷脂(GC)的抗体进行的双重标记实验中,在所有检测的年龄段,至少95%的少突胶质细胞中这两种抗原共同表达。一小部分相对未分化的细胞先表达一种抗原,再表达另一种抗原。在培养细胞产生的细胞膜片中,CNP和GC的分布不同。CNP高度集中在细胞体、从细胞体延伸到膜片的突起网络以及膜片周边。在膜片主体的某些区域检测不到CNP染色。若有染色,强度也很低。在我们的标记条件下,除了在富含CNP的静脉网络中,GC染色可见于整个细胞膜片。尽管GC是表面成分而髓鞘碱性蛋白(MBP)位于细胞质面,但在相似的膜结构域中可见GC和MBP染色。CNP免疫染色的时间和定位均表明,CNP与GC一样是少突胶质细胞的早期标志物,并支持CNP可能在髓鞘膜中发挥结构作用的观点。用GC和CNP抗体进行的双重标记研究还表明,单一抗原并不总能揭示细胞的真实形态及其发育程度。抗原在细胞膜片中的差异分布表明,它们包含可能反映完整髓鞘情况的结构特化区域。