Kobayashi Ryosuke, Chambers James K, Yoshida Keiko, Nakamura Takashi, Yasuno Kyohei, Uchida Kazuyuki, Kamiie Junichi, Shirota Kinji
J Zoo Wildl Med. 2016 Jun;47(2):663-6. doi: 10.1638/2015-0245.1.
Lipoprotein glomerulopathy (LPG) is a rare human glomerular disease caused by abnormal lipid metabolism. Naturally occurring LPG has not been reported in animals. We describe the histopathological characterization of spontaneous LPG-like nephropathy in a captive squirrel ( Sciurus vulgaris ). Macroscopically, swollen glomeruli were distinctively identified as fine white granules in the renal cortex. Histologically, most glomeruli were markedly enlarged with distended capillaries containing faintly eosinophilic and amorphous materials. The amorphous material was negative using the periodic acid-Schiff reaction, periodic acid-methenamine silver stain, or Masson's trichrome stain. Sudan III staining revealed lipid in the materials, and immunohistochemistry demonstrated that the material additionally contained apolipoprotein E. Electron microscopy showed numerous lipid granules and vacuoles of various sizes in the capillary lumina associated with foot process effacement of podocytes. These pathological characteristics bear some resemblance to those of human LPG.
脂蛋白肾小球病(LPG)是一种由脂质代谢异常引起的罕见人类肾小球疾病。在动物中尚未报道过自然发生的LPG。我们描述了一只圈养松鼠(Sciurus vulgaris)自发性LPG样肾病的组织病理学特征。宏观上,肿胀的肾小球在肾皮质中明显表现为细小的白色颗粒。组织学上,大多数肾小球明显增大,毛细血管扩张,含有淡嗜酸性和无定形物质。使用过碘酸-希夫反应、过碘酸-亚甲胺银染色或马松三色染色,无定形物质呈阴性。苏丹III染色显示材料中存在脂质,免疫组织化学表明该材料还含有载脂蛋白E。电子显微镜显示毛细血管腔内有许多大小不一的脂质颗粒和空泡,伴有足细胞足突消失。这些病理特征与人类LPG有一些相似之处。