FitzGerald P G, Bok D, Horwitz J
Curr Eye Res. 1985 Nov;4(11):1203-18. doi: 10.3109/02713688509003365.
The Main Intrinsic Polypeptide (MIP) of the ocular lens fiber cell plasma membrane was immunocytochemically localized at the ultrastructural level on ultrathin frozen sections of rat lens, and on extracted, gradient-purified bovine lens membranes. The results indicate that both the junctional and non-junctional membrane domains of the cortical lens fiber cell are MIP immunoreactive. Frozen thin section immunocytochemistry of the lens epithelium and hepatocytes, also using anti-MIP antibodies, revealed that these cells, and their intercellular junctions, are not MIP-immunoreactive. From these findings we conclude that 1) MIP, a putative fiber cell junctional protein, is present throughout the plasma membrane of the lens fiber cell, and is not confined to the fiber cell junctional domain, 2) MIP is not a detectable component of the lens epithelial cell membrane, or its intercellular junctions, 3) MIP is not detectable in gap junctions of hepatocytes.
利用免疫细胞化学方法,在大鼠晶状体超薄冰冻切片以及提取并经梯度纯化的牛晶状体膜上,在超微结构水平对眼晶状体纤维细胞质膜的主要内在多肽(MIP)进行了定位。结果表明,晶状体皮质纤维细胞的连接膜区和非连接膜区均有MIP免疫反应性。同样使用抗MIP抗体对晶状体上皮细胞和肝细胞进行冰冻薄切片免疫细胞化学分析,结果显示这些细胞及其细胞间连接并无MIP免疫反应性。从这些发现我们得出以下结论:1)MIP作为一种假定的纤维细胞连接蛋白,存在于晶状体纤维细胞的整个质膜中,并不局限于纤维细胞连接区;2)MIP不是晶状体上皮细胞膜及其细胞间连接的可检测成分;3)在肝细胞的缝隙连接中检测不到MIP。