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采用“体内冷冻技术”对不同血流动力学条件下活体小鼠肾小球中的血清蛋白进行免疫定位。

Immunolocalization of serum proteins in living mouse glomeruli under various hemodynamic conditions by "in vivo cryotechnique".

作者信息

Li Zilong, Ohno Nobuhiko, Terada Nobuo, Ohno Shinichi

机构信息

Department of Anatomy, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Tamaho, Yamanashi, 409-3898, Japan.

出版信息

Histochem Cell Biol. 2006 Sep;126(3):399-406. doi: 10.1007/s00418-006-0175-4. Epub 2006 Apr 7.

Abstract

Distribution of serum proteins in renal glomeruli is important for histopathology in medical and biological fields, but mechanisms of their passage through glomerular capillary loops (GCL) are still difficult to clarify. We have tried to visualize topographical changes of the serum proteins passing through GCL by "in vivo cryotechnique" in combination with immunohistochemistry. Albumin and immunoglobulin G (IgG), Ig kappa light chain and IgG1 heavy chain were mainly immunolocalized in GCL, but not colocalized with zonula occludens-1 (ZO-1) under normotensive condition. Under heart-arrest condition and in quick-frozen fresh tissues, albumin and kappa light chain were immunolocalized in Bowman's space, indicating their passage caused by the stoppage of blood supply. However, under acute hypertensive condition, they were more clearly immunolocalized along basement membranes and in the Bowman's space, indicating their increased passage through GCL. IgG was also more clearly localized in mesangial areas under acute hypertension, compared with that under the normotensive or heart-arrest condition. This study is the first direct visualization for glomerular passage of serum proteins under abnormal hemodynamic conditions by the "in vivo cryotechnique", and the experimental protocol will be useful for morphofunctional examination of living mouse GCL and immunohistochemical analyses of dynamically changing proteins.

摘要

血清蛋白在肾小球中的分布在医学和生物学领域的组织病理学中具有重要意义,但其通过肾小球毛细血管袢(GCL)的机制仍难以阐明。我们试图通过“体内冷冻技术”结合免疫组织化学来观察血清蛋白通过GCL的拓扑变化。在正常血压条件下,白蛋白、免疫球蛋白G(IgG)、Ig κ轻链和IgG1重链主要免疫定位在GCL中,但不与紧密连接蛋白-1(ZO-1)共定位。在心脏骤停条件下和速冻新鲜组织中,白蛋白和κ轻链免疫定位在鲍曼间隙,表明它们的通过是由血液供应停止引起的。然而,在急性高血压条件下,它们沿基底膜和鲍曼间隙的免疫定位更明显,表明它们通过GCL的量增加。与正常血压或心脏骤停条件相比,急性高血压下IgG在系膜区的定位也更明显。本研究首次通过“体内冷冻技术”直接观察了异常血流动力学条件下血清蛋白在肾小球中的通过情况,该实验方案将有助于对活体小鼠GCL进行形态功能检查以及对动态变化蛋白进行免疫组织化学分析。

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