Renal Expression of CLC-5 and Megalin/Cubilin in Dent-1 Disease With Nonsense Mutations of CLCN5 Gene. (July 2022)
- Record Type:
- Journal Article
- Title:
- Renal Expression of CLC-5 and Megalin/Cubilin in Dent-1 Disease With Nonsense Mutations of CLCN5 Gene. (July 2022)
- Main Title:
- Renal Expression of CLC-5 and Megalin/Cubilin in Dent-1 Disease With Nonsense Mutations of CLCN5 Gene
- Authors:
- Zhai, Panpan
Lv, Weigang
Yang, Xiaoqing
Huang, Yanjie
Zhai, Wensheng
Ren, Xianqing
Zhang, Xia
Yang, Meng
Zhang, Jian
Guo, Ting
Bai, Minghui
Yang, Yueli
Ding, Ying
Huang, Yanshi - Abstract:
- The study aims to explore the clinicopathological features and whether the nonsense mutations of CLCN5 gene have effect on the renal expression of CLC-5 protein and megalin/cubilin complex in children with Dent-1 disease. The clinicopathological features and genetic examination of three patients with Dent-1 disease were investigated. The expression of CLC-5 and megalin/cubilin complex in renal tissues was detected by using immunohistochemistry method. Urinary albumin, α1-microglobulin, β2-microglobulin, retinol binding protein, and calcium levels were measured by immunonephelometry. Urinary calcium and low molecular weight proteinuria (LMWP) were enhanced in three patients, and two presented with nephrotic range proteinuria. Focal glomerular obsolescence, minor tubulointerstitial injury, and focal calcification in corticomedullary junction were found in one patient. Nonsense mutations of CLCN5 gene from their mothers were identified in all three patients with Dent-1 disease; however, the expression of CLC-5 protein was not decreased in renal tubular cells. As the receptor complex of albumin and LMWP reabsorption, the expression of megalin/cubilin in the brush border of proximal tubules was decreased in Dent-1 patients. Even if the renal CLC-5 protein is expressed normally, the reduced expression of megalin/cubilin in the brush border of renal proximal tubules may be helpful to understand the physiopathology of Dent-1 disease with nonsense mutations of CLCN5 gene.
- Is Part Of:
- Pediatric and developmental pathology. Volume 25:Number 4(2022)
- Journal:
- Pediatric and developmental pathology
- Issue:
- Volume 25:Number 4(2022)
- Issue Display:
- Volume 25, Issue 4 (2022)
- Year:
- 2022
- Volume:
- 25
- Issue:
- 4
- Issue Sort Value:
- 2022-0025-0004-0000
- Page Start:
- 397
- Page End:
- 403
- Publication Date:
- 2022-07
- Subjects:
- Dent-1 disease -- clinicopathological features -- CLC-5 -- megalin/cubilin complex
Pediatric pathology -- Periodicals
Children -- Diseases -- Periodicals
Diagnosis, Laboratory -- Periodicals
Abnormalities, Human -- Periodicals
Child development -- Periodicals
Pediatrics -- Periodicals
616.07 - Journal URLs:
- http://link.springer-ny.com/link/service/journals/10024/index.htm ↗
http://www.pedpath.org/ ↗
http://www.spponline.org/publications2.asp#01 ↗
https://uk.sagepub.com/en-gb/eur/pediatric-and-developmental-pathology/journal202544 ↗
http://www.sagepublications.com/ ↗ - DOI:
- 10.1177/10935266211065554 ↗
- Languages:
- English
- ISSNs:
- 1093-5266
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.528500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21653.xml