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与免疫金标记核心蛋白相比,用铜叶绿酸蓝侧链染色法对基底膜中硫酸乙酰肝素蛋白聚糖进行定位。

Localization of heparan sulfate proteoglycan in basement membrane by side chain staining with cuprolinic blue as compared with core protein labeling with immunogold.

作者信息

Chan F L, Inoue S, Leblond C P

机构信息

Department of Anatomy, McGill University, Montreal, Quebec, Canada.

出版信息

J Histochem Cytochem. 1992 Oct;40(10):1559-72. doi: 10.1177/40.10.1527375.

Abstract

We localized heparan sulfate proteoglycan (HSPG) in the basement membranes of ciliary epithelium and plantar epidermis, using Cuprolinic blue to stain its side chains and an immunogold procedure to detect its core protein. In accord with most of the literature, staining with Cuprolinic blue in glutaraldehyde fixative yielded three to five times as many reaction products along the two surfaces than along the center of the lamina densa, whereas immunogold labeling for the core protein after formaldehyde fixation yielded about twice as many gold particles over the center than along the surfaces of the lamina densa. It therefore appeared that HSPG side chains predominated outside, and the core protein within, the lamina densa. To find out whether the discrepancy was true or was an artifact caused by differences in processing, we attempted to combine the two approaches on the same material. This was found possible when Cuprolinic blue was used in formaldehyde fixative, embedding was in LR White, and immunogold labeling was performed on thin sections as usual. Under these conditions, both Cuprolinic blue reaction products and immunogold particles predominated over the lamina densa in the two basement membranes under study. Moreover, evidence was present that reaction products and immunogold particles either overlapped each other or were closely associated. The lens capsule (a thick basement membrane) also showed their co-localization. The discrepancy initially observed between side chains and core protein location was attributed to differences in processing, since Cuprolinic blue staining had been carried out in the course of glutaraldehyde fixation whereas immunogold labeling was done after formaldehyde fixation. The results lead to two conclusions. First, processing differences may alter the localization of HSPG and possibly other proteoglycans. Second, both HSPG side chains and core protein are localized in the same sites within basement membrane.

摘要

我们利用铜叶绿酸蓝对硫酸乙酰肝素蛋白聚糖(HSPG)的侧链进行染色,并采用免疫金法检测其核心蛋白,从而对睫状上皮和足底表皮基底膜中的HSPG进行定位。与大多数文献一致,在戊二醛固定剂中用铜叶绿酸蓝染色时,致密板两侧表面产生的反应产物数量是致密板中心的三到五倍,而甲醛固定后对核心蛋白进行免疫金标记时,致密板中心产生的金颗粒数量约为致密板表面的两倍。因此,HSPG侧链似乎在致密板外侧占主导,而核心蛋白在致密板内侧占主导。为了弄清楚这种差异是真实存在的还是由处理过程中的差异导致的假象,我们尝试在同一份材料上结合这两种方法。当在甲醛固定剂中使用铜叶绿酸蓝、用LR White进行包埋并像往常一样在薄切片上进行免疫金标记时,发现这是可行的。在这些条件下,在所研究的两个基底膜中,铜叶绿酸蓝反应产物和免疫金颗粒在致密板上均占主导。此外,有证据表明反应产物和免疫金颗粒相互重叠或紧密相关。晶状体囊膜(一种厚基底膜)也显示出它们的共定位。最初观察到的侧链和核心蛋白定位之间的差异归因于处理过程中的差异,因为铜叶绿酸蓝染色是在戊二醛固定过程中进行的,而免疫金标记是在甲醛固定后进行的。这些结果得出两个结论。第一,处理过程的差异可能会改变HSPG以及可能其他蛋白聚糖的定位。第二,HSPG侧链和核心蛋白都定位在基底膜内的相同位点。

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