Zhou D, Ohno N, Terada N, Li Z, Morita H, Inui K, Yoshimura A, Ohno S
Department of Anatomy, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo-city, Yamanashi, Japan.
Histol Histopathol. 2007 Feb;22(2):137-45. doi: 10.14670/HH-22.137.
Immunohistochemical analyses on local distributions of serum proteins in living mouse kidneys are usually difficult to examine with conventional preparation methods. By using our "in vivo cryotechnique" combined with freeze-substitution, we have checked immunolocalizations of the serum proteins in nephrons of bovine serum albumin (BSA)-overload mice, and compared them with those obtained by the conventional preparation methods. In two days of daily BSA-injected mice, the immunolocalization of BSA could be observed in Bowman's space and urinary tubules with their overt proteinuria, where another endogenous mouse albumin was similarly immunolocalized. The leakage of BSA and mouse albumin in Bowman's space and their reabsorption into proximal tubules were detected in 55% of nephrons, where no leakage of immunoglobulin G1 (IgG1) was detected. However, the leakage of IgG1, in addition to BSA and mouse albumin, was detected in the other nephrons. By carefully examining immunolocalizations of BSA and IgG1, they were obviously different from those obtained by the conventional preparation methods without normal blood circulation into the kidneys. The immunolocalizations of both BSA and mouse serum proteins could be directly analyzed with the "in vivo cryotechnique", suggesting that functional damage to glomerular filtration barriers are different at early stages of the BSA-overload mouse model, depending on each nephron of living mice.
对活体小鼠肾脏中血清蛋白的局部分布进行免疫组织化学分析,通常很难用传统的制备方法来检测。通过使用我们的“体内冷冻技术”并结合冷冻置换,我们检查了牛血清白蛋白(BSA)过载小鼠肾单位中血清蛋白的免疫定位,并将其与通过传统制备方法获得的结果进行了比较。在每天注射BSA的小鼠中,两天后,在出现明显蛋白尿的鲍曼氏间隙和肾小管中可观察到BSA的免疫定位,另一种内源性小鼠白蛋白也有类似的免疫定位。在55%的肾单位中检测到鲍曼氏间隙中BSA和小鼠白蛋白的泄漏以及它们被近端小管重吸收,其中未检测到免疫球蛋白G1(IgG1)的泄漏。然而,在其他肾单位中,除了BSA和小鼠白蛋白外,还检测到了IgG1的泄漏。通过仔细检查BSA和IgG1的免疫定位,它们明显不同于在肾脏没有正常血液循环的情况下通过传统制备方法获得的结果。利用“体内冷冻技术”可以直接分析BSA和小鼠血清蛋白的免疫定位,这表明在BSA过载小鼠模型的早期阶段,肾小球滤过屏障的功能损伤因活体小鼠的每个肾单位而异。