Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
Department of Gynaecology and Obstetrics, University Hospital Regensburg, Regensburg, Germany.
J Histochem Cytochem. 2018 Jan;66(1):7-22. doi: 10.1369/0022155417737975. Epub 2017 Oct 27.
The homeostatic chemokine receptor CCR7 serves as key molecule in lymphocyte homing into secondary lymphoid tissues. Previous experiments from our group identified CCR7 also to be expressed by human mesangial cells. Exposing cultured human mesangial cells to the receptor ligand CCL21 revealed a positive effect on these cells regarding proliferation, migration, and survival. In the present study, we localized CCR7 and CCL21 during murine nephrogenesis. Analyzing wild-type and CCR7 deficient (CCR7) mice, we observed a retarded glomerulogenesis during renal development and a significantly decreased mesangial cellularity in adult CCR7 mice, as a consequence of less mesangial cell proliferation between embryonic day E17.5 and week 5 postpartum. Cell proliferation assays and cell-wounding experiments confirmed reduced proliferative and migratory properties of mesangial cells cultured from CCR7 kidneys. To further emphasize the role of CCR7 as important factor for mesangial biology, we examined the chemokine receptor expression in rats after induction of a mesangioproliferative glomerulonephritis. Here, we demonstrated for the first time that extra- and intraglomerular mesangial cells that were CCR7-negative in control rats exhibited a strong CCR7 expression during the phase of mesangial repopulation and proliferation.
稳态趋化因子受体 CCR7 是淋巴细胞归巢至次级淋巴组织的关键分子。我们小组的先前实验表明 CCR7 也在人肾小球系膜细胞中表达。将 CCR7 的配体 CCL21 暴露于培养的人肾小球系膜细胞中,发现其对这些细胞的增殖、迁移和存活有积极影响。在本研究中,我们在鼠肾发生过程中定位了 CCR7 和 CCL21。分析野生型和 CCR7 缺陷型(CCR7)小鼠,我们观察到在肾脏发育过程中肾小球发生延迟,并且在成年 CCR7 小鼠中肾小球系膜细胞数量明显减少,这是由于胚胎期 E17.5 至产后第 5 周之间的系膜细胞增殖减少所致。细胞增殖测定和细胞划痕实验证实了从 CCR7 肾脏培养的系膜细胞增殖和迁移能力降低。为了进一步强调 CCR7 作为系膜生物学重要因素的作用,我们在诱导系膜增生性肾小球肾炎后检查了大鼠的趋化因子受体表达。在这里,我们首次证明,在对照大鼠中,肾小球内和肾小球外的系膜细胞在系膜细胞再增殖和增殖阶段 CCR7 表达为阴性。