足细胞
狼疮性肾炎
医学
祖细胞
尼福林
复合杂合度
内科学
癌症研究
等位基因
肾
遗传学
蛋白尿
基因
生物
干细胞
疾病
作者
Paola Romagnani,Sabrina Giglio,Maria Lucia Angelotti,Aldesia Provenzano,Francesca Becherucci,Benedetta Mazzinghi,Susanna Müller,Kerstin Amann,Marc Weidenbusch,Simone Romoli,Elena Lazzeri,Hans‐Joachim Anders
摘要
Often the cause of refractory lupus nephritis (RLN) remains unclear. We performed next-generation sequencing for podocyte genes in an RLN patient and identified compound heterozygosity for APOL1 risk alleles G1 and G2 and a novel homozygous c.[1049C>T]+[1049C>T] NPHS1 gene variant of unknown significance. To test for causality renal progenitor cells isolated from urine of this patient were differentiated into podocytes in vitro. Podocytes revealed aberrant nephrin trafficking, cytoskeletal structure and lysosomal leakage, and increased detachment as compared with podocytes isolated from controls. Thus, lupus podocytopathy can be confirmed as a cause of RLN by functional genetics on patient-derived podocytes.
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