Niendorf A, Arps H, Sieck M, Dietel M
Acta Endocrinol Suppl (Copenh). 1987;281:207-11. doi: 10.1530/acta.0.114s207.
Localization of PTH-binding sites has been examined in intact kidney sections and cultured cells derived from bovine kidney cortex. Tissue sections were incubated with 10(-7) M bovine PTH (1-84) for 2 h, cells for 15 min, at 37 degrees C. Visualization of PTH-binding was achieved by immunocytochemistry using a carboxy-terminal specific anti-PTH antiserum (S 478). For control, cell culture incubations were performed applying competitively 10(-7) bovine PTH (1-84) and a 10-fold excess of synthetic 1-34 PTH fragment, not antigenic for S 478. This resulted in a lack of staining. PTH-binding was found in all cells of the proximal and the distal tubule, and with less intensity in the thick ascending limb of Henle's loop. In collecting ducts a PTH specific staining was also present, which was confined to single cells localized between others without PTH binding sites. No staining was seen in glomerula, the thin limb of Henle's loop, in blood vessels, and in connective tissue. The data suggest that large parts of the nephron contain PTH-binding sites, although in different amounts. This is in agreement with the numerous actions of PTH in the kidney. In the collecting segment a distinct cell-to-cell difference was disclosed indicative for different functional states or cellular heterogeneity.
已在完整的肾脏切片以及源自牛肾皮质的培养细胞中研究了甲状旁腺激素(PTH)结合位点的定位。将组织切片与10⁻⁷M牛PTH(1-84)在37℃下孵育2小时,细胞孵育15分钟。使用羧基末端特异性抗PTH抗血清(S 478)通过免疫细胞化学实现PTH结合的可视化。作为对照,在细胞培养孵育中竞争性地应用10⁻⁷牛PTH(1-84)和10倍过量的合成1-34 PTH片段,该片段对S 478无抗原性。这导致缺乏染色。在近端小管和远端小管的所有细胞中均发现PTH结合,在亨氏袢的厚升支中结合强度较低。在集合管中也存在PTH特异性染色,其局限于位于其他无PTH结合位点的细胞之间的单个细胞。在肾小球、亨氏袢细段、血管和结缔组织中未见染色。数据表明,肾单位的大部分含有PTH结合位点,尽管数量不同。这与PTH在肾脏中的多种作用一致。在集合段中发现了明显的细胞间差异,表明存在不同的功能状态或细胞异质性。