Žužul Sani, Kelam Nela, Racetin Anita, Kovačević Petra, Konjevoda Suzana, Filipović Natalija, Pavlović Nikola, Vukojević Katarina
Clinic for Surgery, Clinical Hospital Firule, 21 000 Split, Croatia.
Department of Anatomy, Histology and Embryology, School of Medicine, University of Split, 21 000 Split, Croatia.
Biomedicines. 2024 Jul 11;12(7):1542. doi: 10.3390/biomedicines12071542.
Our study examines the immunoexpression patterns of Megalin, Cubilin, Caveolin-1, Gipc1 and Dab2IP in the embryonic development (E) and postnatal (P) mouse kidney, with a focus on differentiating patterns between wild-type (wt) and , () mice. Immunofluorescence revealed raised immunoexpression of receptors Megalin and Cubilin at the ampulla/collecting ducts and convoluted tubules across all developmental stages, with the most prominent immunoexpression observed in the convoluted tubules and the parietal epithelium of the Bowman's capsule. Quantitative analysis showed a higher percentage of Megalin and Cubilin in wt compared to mice at E13.5. Co-expression of Megalin and Cubilin was observed at the apical membrane of convoluted tubules and the parietal layer of the Bowman's capsule. The staining intensity of Megalin varied across developmental stages, with the strongest reactivity observed at the ampulla and collecting ducts at embryonic day (E) 13.5 in wt mice. In contrast, Caveolin-1 exhibited high immunoexpression in the metanephric mesenchyme, blood vessels, and the border area between the metanephric mesenchyme and renal vesicle, with a decrease in immunoexpression as development progressed. Gipc1 showed diffuse cytoplasmic staining in metanephric mesenchyme, convoluted tubules and collecting ducts, with significant differences in immunoexpression between wild-type and mice at both investigated embryonic time points. Dab2IP immunofluorescent staining was most prominent in renal vesicle/glomeruli and ampulla/collecting ducts at E13.5, with mild staining intensity observed in the distal convoluted tubules postnatally. Our findings elucidate distinct immunoexpression of patterns and potential parts of these proteins in the development and function of the kidney, highlighting the importance of further investigation into their regulatory mechanisms.
我们的研究检测了Megalin、Cubilin、小窝蛋白-1(Caveolin-1)、Gipc1和Dab2IP在胚胎发育(E)期和出生后(P)小鼠肾脏中的免疫表达模式,重点是区分野生型(wt)和[此处原文缺失具体基因类型]小鼠之间的表达模式差异。免疫荧光显示,在所有发育阶段,受体Megalin和Cubilin在壶腹/集合管和曲管处的免疫表达均升高,其中在曲管和鲍曼囊壁层的免疫表达最为显著。定量分析显示,与[此处原文缺失具体基因类型]小鼠相比,野生型小鼠在E13.5时Megalin和Cubilin的百分比更高。在曲管顶端膜和鲍曼囊壁层观察到Megalin和Cubilin的共表达。Megalin的染色强度在不同发育阶段有所变化,野生型小鼠在胚胎第13.5天(E13.5)时,壶腹和集合管处的反应性最强。相比之下,小窝蛋白-1在肾间充质、血管以及肾间充质和肾小泡之间的边界区域表现出高免疫表达,随着发育进程免疫表达降低。Gipc1在肾间充质、曲管和集合管中呈弥漫性细胞质染色,在两个研究的胚胎时间点,野生型和[此处原文缺失具体基因类型]小鼠之间的免疫表达存在显著差异。Dab2IP免疫荧光染色在E13.5时在肾小泡/肾小球和壶腹/集合管中最为显著,出生后在远曲小管中观察到轻度染色强度。我们的研究结果阐明了这些蛋白质在肾脏发育和功能中的独特免疫表达模式及潜在作用,强调了进一步研究其调控机制的重要性。