Segment-specific c-ErbB2 expression in human autosomal recessive polycystic kidney disease

被引:0
|
作者
Nakanishi, K
Sweeney, WE
Avner, ED
机构
[1] Rainbow Babies & Childrens Hosp, Dept Pediat, Rainbow Ctr Childhood PKD, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Cleveland, OH 44106 USA
来源
关键词
D O I
暂无
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
c-ErbB2 (also referred to as Neu or HER2), a transmembrane glycoprotein with intrinsic tyrosine kinase activity, is structurally related to epidermal growth factor receptor (EGFR) and forms active heterodimers with EGFR as well as other members of the EGFR family. c-ErbB2 is reported to mediate differentiation and proliferation in epithelial cells and is expressed in a tissue-specific and developmental stage-specific manner. Given the role of EGFR in cystic renal epithelial hyperplasia and the immature phenotype of cystic renal epithelial cells, the segment-specific expression pattern of c-ErbB2 in human autosomal recessive polycystic kidney disease (ARPKD) was examined in nine ARPKD kidney specimens ranging from gestational age 17 wk through postnatal age 4 wk. c-ErbB2 staining of human ARPKD samples showed increased expression with increasing gestational age compared with normal human fetal and postnatal kidneys. This increased c-ErbB2 expression was primarily localized to the apical surfaces of cystic collecting tubule cells, similar to the pattern of EGFR expression, and paralleled collecting tubular cyst formation and growth.
引用
收藏
页码:379 / 384
页数:6
相关论文
共 50 条
  • [21] Boy with autosomal recessive polycystic kidney and autosomal dominant polycystic liver disease
    Andrea Zingg-Schenk
    Jürg Caduff
    Silvia Azzarello-Burri
    Carsten Bergmann
    Joost P. H. Drenth
    Thomas J. Neuhaus
    Pediatric Nephrology, 2012, 27 : 1197 - 1200
  • [22] Cyst fluid composition in human autosomal recessive polycystic kidney disease
    Rohatgi, R
    Zavilowitz, B
    Vergara, M
    Woda, C
    Kim, P
    Satlin, LM
    PEDIATRIC NEPHROLOGY, 2005, 20 (04) : 552 - 553
  • [23] Cyst fluid composition in human autosomal recessive polycystic kidney disease
    Rajeev Rohatgi
    Beth Zavilowitz
    Marcela Vergara
    Craig Woda
    Paul Kim
    Lisa M. Satlin
    Pediatric Nephrology, 2005, 20 : 552 - 553
  • [24] Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?
    Jayanthi Chandar
    Jennifer Garcia
    Lydia Jorge
    Akin Tekin
    Pediatric Nephrology, 2015, 30 : 1233 - 1242
  • [25] Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?
    Chandar, Jayanthi
    Garcia, Jennifer
    Jorge, Lydia
    Tekin, Akin
    PEDIATRIC NEPHROLOGY, 2015, 30 (08) : 1233 - 1242
  • [26] Polycystic kidney diseases : a gene identified in autosomal recessive polycystic kidney disease
    Gilgenkrantz, S
    M S-MEDECINE SCIENCES, 2002, 18 (05): : 530 - 532
  • [27] Clinical manifestations of autosomal recessive polycystic kidney disease
    Hoyer, Peter F.
    CURRENT OPINION IN PEDIATRICS, 2015, 27 (02) : 186 - 192
  • [28] Clinical aspects of autosomal recessive polycystic kidney disease
    Dias, N. F.
    Lanzarini, V
    Onuchic, L. F.
    Koch, V
    PEDIATRIC NEPHROLOGY, 2007, 22 (12) : 2154 - 2154
  • [29] Liver Involvement in Autosomal Recessive Polycystic Kidney Disease
    Bramlage, Mary Alexandra
    Sang, Jessica L.
    Lewis, Jason
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2022, 117 (10): : S1981 - S1981
  • [30] Genetic characterization of autosomal recessive polycystic kidney disease
    Casey J.
    Nature Clinical Practice Nephrology, 2006, 2 (6): : 295 - 295