Disruption of Robo2-Baiap2 integrated signaling drives cystic disease

Qinggang Li, Shaoyuan Cui, Qian Ma, Ying Liu, Hongyu Yu, Guangrui Geng, Ewud Agborbesong, Chongyu Ren, Kai Wei, Yingjie Zhang, Jurong Yang, Xueyuan Bai, Guangyan Cai, Yuansheng Xie, Xiaogang Li, Xiangmei Chen

Research output: Contribution to journalArticle

Abstract

Hereditary renal cystic diseases are characterized by defects in primary cilia of renal tubular epithelial cells and abnormality of tubular epithelium, which ultimately result in the development of renal cysts. However, the mechanism leading from abnormality of the tubular epithelium to cystogenesis is not well understood. In this report, we demonstrate a critical role for Robo2 in regulating epithelial development, including ciliogenesis, polarization, and differentiation. We found that Robo2 deficiency results in cystic kidneys, and the cyst cells showed defective cilia and polarity defects in tubular epithelium. The cyst cells, less than terminally differentiated, continue to proliferate. We further established that Robo2 works with p53 as well as polarity and ciliary proteins (Par3, PKCς, ZO-2, and Claudin-2) to regulate these processes. Robo2 binds to Baiap2 (also known as IRSp53) through the IRSp53/MIM homology domain in renal epithelial cells. This binding allows Robo2 to phosphorylate MDM2 at Ser166 via Baiap2 and maintain p53 homeostasis. Disruption of the Robo2-Baiap2 complex causes MDM2 to be subjected to dephosphorylation, leading to a high level of active p53, and initiated p53-mediated cellular senescence via p21 and decreased the expression of ZO-1, ZO-2, PKC?, Par3, and Claudin-2 proteins, resulting in defects in epithelial development, including ciliogenesis, polarization, and differentiation. Importantly, double knockout of Robo2 and p53 rescued all the epithelial defects in kidneys compared with those in Robo2-knockout kidneys. Taken together, the present results demonstrate that Robo2 deficiency causes renal cystic disease, which is largely dependent on defective Robo2-Baiap2 integrated signaling in kidneys.

Original languageEnglish (US)
Article numbere127602
JournalJCI Insight
Volume4
Issue number18
DOIs
StatePublished - Sep 19 2019

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Cystic Kidney Diseases
Kidney
Claudin-2
Cysts
Epithelium
Cilia
Epithelial Cells
Claudins
Cell Aging
Homeostasis
Proteins

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Li, Q., Cui, S., Ma, Q., Liu, Y., Yu, H., Geng, G., ... Chen, X. (2019). Disruption of Robo2-Baiap2 integrated signaling drives cystic disease. JCI Insight, 4(18), [e127602]. https://doi.org/10.1172/jci.insight.127602

Disruption of Robo2-Baiap2 integrated signaling drives cystic disease. / Li, Qinggang; Cui, Shaoyuan; Ma, Qian; Liu, Ying; Yu, Hongyu; Geng, Guangrui; Agborbesong, Ewud; Ren, Chongyu; Wei, Kai; Zhang, Yingjie; Yang, Jurong; Bai, Xueyuan; Cai, Guangyan; Xie, Yuansheng; Li, Xiaogang; Chen, Xiangmei.

In: JCI Insight, Vol. 4, No. 18, e127602, 19.09.2019.

Research output: Contribution to journalArticle

Li, Q, Cui, S, Ma, Q, Liu, Y, Yu, H, Geng, G, Agborbesong, E, Ren, C, Wei, K, Zhang, Y, Yang, J, Bai, X, Cai, G, Xie, Y, Li, X & Chen, X 2019, 'Disruption of Robo2-Baiap2 integrated signaling drives cystic disease', JCI Insight, vol. 4, no. 18, e127602. https://doi.org/10.1172/jci.insight.127602
Li, Qinggang ; Cui, Shaoyuan ; Ma, Qian ; Liu, Ying ; Yu, Hongyu ; Geng, Guangrui ; Agborbesong, Ewud ; Ren, Chongyu ; Wei, Kai ; Zhang, Yingjie ; Yang, Jurong ; Bai, Xueyuan ; Cai, Guangyan ; Xie, Yuansheng ; Li, Xiaogang ; Chen, Xiangmei. / Disruption of Robo2-Baiap2 integrated signaling drives cystic disease. In: JCI Insight. 2019 ; Vol. 4, No. 18.
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abstract = "Hereditary renal cystic diseases are characterized by defects in primary cilia of renal tubular epithelial cells and abnormality of tubular epithelium, which ultimately result in the development of renal cysts. However, the mechanism leading from abnormality of the tubular epithelium to cystogenesis is not well understood. In this report, we demonstrate a critical role for Robo2 in regulating epithelial development, including ciliogenesis, polarization, and differentiation. We found that Robo2 deficiency results in cystic kidneys, and the cyst cells showed defective cilia and polarity defects in tubular epithelium. The cyst cells, less than terminally differentiated, continue to proliferate. We further established that Robo2 works with p53 as well as polarity and ciliary proteins (Par3, PKCς, ZO-2, and Claudin-2) to regulate these processes. Robo2 binds to Baiap2 (also known as IRSp53) through the IRSp53/MIM homology domain in renal epithelial cells. This binding allows Robo2 to phosphorylate MDM2 at Ser166 via Baiap2 and maintain p53 homeostasis. Disruption of the Robo2-Baiap2 complex causes MDM2 to be subjected to dephosphorylation, leading to a high level of active p53, and initiated p53-mediated cellular senescence via p21 and decreased the expression of ZO-1, ZO-2, PKC?, Par3, and Claudin-2 proteins, resulting in defects in epithelial development, including ciliogenesis, polarization, and differentiation. Importantly, double knockout of Robo2 and p53 rescued all the epithelial defects in kidneys compared with those in Robo2-knockout kidneys. Taken together, the present results demonstrate that Robo2 deficiency causes renal cystic disease, which is largely dependent on defective Robo2-Baiap2 integrated signaling in kidneys.",
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AU - Geng, Guangrui

AU - Agborbesong, Ewud

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AU - Yang, Jurong

AU - Bai, Xueyuan

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