Christensen E I, Nielsen S, Moestrup S K, Borre C, Maunsbach A B, de Heer E, Ronco P, Hammond T G, Verroust P
Department of Cell Biology, University of Aarhus, Denmark.
Eur J Cell Biol. 1995 Apr;66(4):349-64.
The subcellular distribution and segmental variations in location of gp330, a scavenger receptor for filtered proteins in renal proximal tubules, was analyzed. Kidney tissue from rats (4 different strains), rabbits and humans were analyzed by light- and electron microscope immunocytochemistry, using cryosections or Lowicryl sections from cryosubstituted tissue. Gp330 was located mainly in apical coated pits, small and large endocytic vacuoles and in dense apical tubules in the proximal tubule cells. The labeling density was markedly higher in segments 1 and 2 as compared to segment 3 of the proximal tubule. In addition to the location in the early part of the endocytic pathway, gp330 was also present in lysosomes, especially in segments 1 and 2. The lysosomal labeling was not restricted to the membrane, but was also seen in the matrix. Localization of gp330 in lysosomes was confirmed on sections from purified lysosomal fractions from rat renal cortex. The brush border localization of gp330 in proximal tubules exhibited a characteristic segmental variation. In the initial part of segment 1, there was virtually no brush border labeling. In the remaining part of segment 1 and in segment 2, there was a distinct but sometimes patchy labeling of the brush border. In segment 3, groups of microvilli of approximately 10 as seen in sections were intensively labeled from bottom to tip and there were often more than one of these groups on a single cell, the remaining microvilli were unlabeled. No differences in the cellular and subcellular localization of gp330 were observed between species or rat strains. In conclusion, the present study demonstrates that in addition to its location in the early endocytic and recycling pathway, gp330 is also present in microvilli and the protein and degradation products thereof is present in lysosomes, consistent with its role as a protein scavenger receptor.
分析了肾近端小管中滤过蛋白的清道夫受体gp330的亚细胞分布及定位的节段性变化。采用冷冻切片或低温替代组织的Lowicryl切片,通过光镜和电镜免疫细胞化学方法分析了大鼠(4种不同品系)、兔和人的肾组织。Gp330主要位于近端小管细胞的顶端被膜小窝、大小不等的内吞小泡以及致密的顶端小管中。与近端小管的第3节段相比,第1和第2节段的标记密度明显更高。除了在内吞途径早期的定位外,gp330也存在于溶酶体中,尤其是在第1和第2节段。溶酶体标记不仅限于膜,在基质中也可见。从大鼠肾皮质纯化的溶酶体组分切片上证实了gp330在溶酶体中的定位。gp330在近端小管刷状缘的定位呈现出特征性的节段性变化。在第1节段的起始部分,几乎没有刷状缘标记。在第1节段的其余部分和第2节段,刷状缘有明显但有时呈斑片状的标记。在第3节段,切片中可见约10根微绒毛组成的簇从底部到顶端被强烈标记,单个细胞上通常有不止一组这样的簇,其余微绒毛未被标记。在不同物种或大鼠品系之间未观察到gp330在细胞和亚细胞定位上的差异。总之,本研究表明,除了在早期内吞和再循环途径中的定位外,gp330也存在于微绒毛中,其蛋白质及其降解产物存在于溶酶体中,这与其作为蛋白质清道夫受体的作用一致。