Kidney-specific upregulation of vitamin D3 target genes in ClC-5 KO mice
Autor: | Anja Schmitt, Tanja Maritzen, Gesa Rickheit, Thomas J. Jentsch |
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Rok vydání: | 2006 |
Předmět: |
Vitamin
medicine.medical_specialty chloride channel Retinoic acid Parathyroid hormone Nephron Kidney Bone and Bones Phosphates chemistry.chemical_compound Kidney Calculi Mice channelopathy Downregulation and upregulation CYP24A1 Calcitriol CYP27B1 Chloride Channels Internal medicine nephrocalcinosis medicine Animals RNA Messenger Intestinal Mucosa Mice Knockout business.industry urogenital system Gene Expression Profiling Up-Regulation Disease Models Animal Low Density Lipoprotein Receptor-Related Protein-2 Proteinuria medicine.anatomical_structure Endocrinology chemistry Gene Expression Regulation Nephrology Knockout mouse business nephrolithiasis |
Zdroj: | Kidney international. 70(1) |
ISSN: | 0085-2538 |
Popis: | Mutations in ClC-5 cause Dent's disease, a disorder associated with low molecular weight proteinuria, hyperphosphaturia, and kidney stones. ClC-5 is a Cl(-)/H(+)-exchanger predominantly expressed in the kidney, where it facilitates the acidification of proximal tubular endosomes. The reduction in proximal tubular endocytosis resulting from a lack of ClC-5 raises the luminal concentration of filtered proteins and peptides like parathyroid hormone (PTH). The increase in PTH may explain the hyperphosphaturia observed in Dent's disease. Expression profiling, quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR), and hormone measurements were used to investigate whether the disruption of ClC-5 affects other signalling pathways. Although the upregulation of 25(OH)(2)-vitamin D(3) 1alpha-hydroxylase and downregulation of vitamin D(3) 24-hydroxylase suggested an increased formation of 1,25(OH)(2)-vitamin D(3), the concentration of this active metabolite was reduced in the serum of ClC-5 knockout (KO) mice. However, target genes of 1,25(OH)(2)-vitamin D(3) were upregulated in KO kidneys. Expression analysis of intestine and bone revealed that the upregulation of 1,25(OH)(2)-vitamin D(3) target genes was kidney intrinsic and not systemic. In spite of reduced serum levels of 1,25(OH)(2)-vitamin D(3) in ClC-5 KO mice, 1,25(OH)(2)-vitamin D(3) is increased in later nephron segments as a consequence of impaired proximal tubular endocytosis. This leads to a kidney-specific stimulation of 1,25(OH)(2)-vitamin D(3) target genes that may contribute to the pathogenesis of Dent's disease. The activation of genes in distal nephron segments by hormones that are normally endocytosed in the proximal tubule may extend to other pathways like those activated by retinoic acid. |
Databáze: | OpenAIRE |
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