CCR7 Is Important for Mesangial Cell Physiology and Repair

Autor: Armin Kurtz, Miriam C. Banas, Claudia R.C. van Roeyen, Bernhard Banas, Simone Wurm, Andreas Steege, Eva-Maria Rom-Jurek
Rok vydání: 2017
Předmět:
0301 basic medicine
Male
medicine.medical_specialty
Receptors
CCR7

Histology
030232 urology & nephrology
610 Medizin
C-C chemokine receptor type 7
chemical and pharmacologic phenomena
anti-Thy1.1 glomerulonephritis
kidney development
mesangiolysis
podocytes

Biology
Kidney
03 medical and health sciences
Chemokine receptor
0302 clinical medicine
Glomerulonephritis
Cell Movement
immune system diseases
Internal medicine
medicine
Animals
570 Biowissenschaften
Biologie

Rats
Wistar

Lymphocyte homing receptor
Receptor
Cells
Cultured

Cell Proliferation
ddc:610
Mesangial cell
Cell growth
Gene Expression Regulation
Developmental

hemic and immune systems
Articles
biological factors
Cell biology
Glomerular Mesangium
Mice
Inbred C57BL

030104 developmental biology
Endocrinology
Mesangiolysis
Anatomy
tissues
Gene Deletion
CCL21
DOI: 10.5283/epub.41731
Popis: 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.
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