Ma A S, Ozers L J
Section of Dermatology, Department of Medicine, The University of Chicago, Illinois 60637, USA.
Arch Dermatol Res. 1996 Sep;288(10):596-603. doi: 10.1007/BF02505262.
The annexins are a family of calcium-dependent phospholipid-binding proteins whose in vitro properties have led to a number of hypotheses suggesting their cellular functions, including membrane fusion in exocytosis and endocytosis. To investigate the topography and possible functions of these proteins we compared the subcellular localization of annexins I, II, IV and VI in skin sections and in cultured epidermal keratinocytes by immunostaining. We found that annexin I staining was in a granular pattern in the monolayer epithelial cells but in an envelope pattern in the stratified keratinocytes. This finding corroborates previous reports that annexin I crosslinks to form cornified envelopes in the mid-epidermis and explains the absence of staining above that level. It is unlikely that this protein is related to exocytosis in the granular layer of the epidermis. In comparison, annexin II staining was also granular and was detected in all nucleated epidermal cells as bands at the cell periphery. However, only annexin II was detected extracellularly among the top layer of cultured cells. The intracellular linear envelope pattern of annexin I and the intercellular pattern of annexin II suggest their interactions with the membrane cytoskeleton in other biological functions. Taken together, both annexins undergo different differentiation-related changes. While methanol fixation enhanced staining of annexin I, it diminished staining of annexin II. Their opposite responses to methanol fixative suggests a different molecular organization of the two annexins with phospholipid in the cell membrane. Annexins IV and VI were predominantly confined to dermal cells including ductal and myoepithelial cells and were not detected in cultured keratinocytes using either cold methanol fixative or prefixation labeling.
膜联蛋白是一类依赖钙的磷脂结合蛋白家族,其体外特性引发了许多关于其细胞功能的假说,包括在胞吐作用和胞吞作用中的膜融合。为了研究这些蛋白的拓扑结构和可能的功能,我们通过免疫染色比较了膜联蛋白I、II、IV和VI在皮肤切片和培养的表皮角质形成细胞中的亚细胞定位。我们发现,膜联蛋白I在单层上皮细胞中呈颗粒状染色模式,但在分层的角质形成细胞中呈包膜状染色模式。这一发现证实了先前的报道,即膜联蛋白I在表皮中部交联形成角化包膜,并解释了该水平以上染色缺失的原因。这种蛋白不太可能与表皮颗粒层中的胞吐作用有关。相比之下,膜联蛋白II的染色也是颗粒状的,并且在所有有核的表皮细胞中作为细胞周边的条带被检测到。然而,在培养细胞的顶层中仅在细胞外检测到膜联蛋白II。膜联蛋白I的细胞内线性包膜模式和膜联蛋白II的细胞间模式表明它们在其他生物学功能中与膜细胞骨架相互作用。总之,两种膜联蛋白都经历了不同的与分化相关的变化。虽然甲醇固定增强了膜联蛋白I的染色,但它减少了膜联蛋白II的染色。它们对甲醇固定剂的相反反应表明两种膜联蛋白在细胞膜中与磷脂的分子组织不同。膜联蛋白IV和VI主要局限于真皮细胞,包括导管和肌上皮细胞,并且使用冷甲醇固定剂或预固定标记在培养的角质形成细胞中未检测到。