Cyst formation in kidney via B-raf signaling in the PKD2 transgenic mice

Eun Young Park, Young Hoon Sung, Moon Hee Yang, Ji Yeun Noh, So Young Park, Tae Young Lee, Yeon Joo Yook, Kyung Hyun Yoo, Kyung Jin Roh, Ingyu Kim, Young Hwan Hwang, Goo Taeg Oh, Je Kyung Seong, Curie Ahn, Han Woong Lee, Jong Hoon Park

Research output: Contribution to journalArticle

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Abstract

The pathogenic mechanisms of human autosomal dominant polycystic kidney disease (ADPKD) have been well known to include the mutational inactivation of PKD2. Although haploinsufficiency and loss of heterozygosity at the Pkd2 locus can cause cyst formation in mice, polycystin-2 is frequently expressed in the renal cyst of human ADPKD, raising the possibility that deregulated activation of PKD2 may be associated with the cystogenesis of human ADPKD. To determine whether increased PKD2 expression is physiologically pathogenic, we generated PKD2-overexpressing transgenic mice. These mice developed typical renal cysts and an increase of proliferation and apoptosis, which are reflective of the human ADPKD phenotype. These manifestations were first observed at six months, and progressed with age. In addition, we found that ERK activation was induced by PKD2 overexpression via B-Raf signaling, providing a possible molecular mechanism of cystogenesis. In PKD2 transgenic mice, B-Raf/MEK/ERK sequential signaling was up-regulated. Additionally, the transgenic human polycystin-2 partially rescues the lethality of Pkd2 knock-out mice and therefore demonstrates that the transgene generated a functional product. Functional strengthening or deregulated activation of PKD2 may be a direct cause of ADPKD. The present study provides evidence for an in vivo role of overexpressed PKD2 in cyst formation. This transgenic mouse model should provide new insights into the pathogenic mechanism of human ADPKD.

Original languageEnglish
Pages (from-to)7214-7222
Number of pages9
JournalJournal of Biological Chemistry
Volume284
Issue number11
DOIs
Publication statusPublished - 2009 Mar 13

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Autosomal Dominant Polycystic Kidney
Transgenic Mice
Cysts
Kidney
Chemical activation
Haploinsufficiency
Loss of Heterozygosity
Mitogen-Activated Protein Kinase Kinases
Transgenes
Knockout Mice
Apoptosis
Phenotype

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Park, E. Y., Sung, Y. H., Yang, M. H., Noh, J. Y., Park, S. Y., Lee, T. Y., ... Park, J. H. (2009). Cyst formation in kidney via B-raf signaling in the PKD2 transgenic mice. Journal of Biological Chemistry, 284(11), 7214-7222. https://doi.org/10.1074/jbc.M805890200
Park, Eun Young ; Sung, Young Hoon ; Yang, Moon Hee ; Noh, Ji Yeun ; Park, So Young ; Lee, Tae Young ; Yook, Yeon Joo ; Yoo, Kyung Hyun ; Roh, Kyung Jin ; Kim, Ingyu ; Hwang, Young Hwan ; Oh, Goo Taeg ; Seong, Je Kyung ; Ahn, Curie ; Lee, Han Woong ; Park, Jong Hoon. / Cyst formation in kidney via B-raf signaling in the PKD2 transgenic mice. In: Journal of Biological Chemistry. 2009 ; Vol. 284, No. 11. pp. 7214-7222.
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title = "Cyst formation in kidney via B-raf signaling in the PKD2 transgenic mice",
abstract = "The pathogenic mechanisms of human autosomal dominant polycystic kidney disease (ADPKD) have been well known to include the mutational inactivation of PKD2. Although haploinsufficiency and loss of heterozygosity at the Pkd2 locus can cause cyst formation in mice, polycystin-2 is frequently expressed in the renal cyst of human ADPKD, raising the possibility that deregulated activation of PKD2 may be associated with the cystogenesis of human ADPKD. To determine whether increased PKD2 expression is physiologically pathogenic, we generated PKD2-overexpressing transgenic mice. These mice developed typical renal cysts and an increase of proliferation and apoptosis, which are reflective of the human ADPKD phenotype. These manifestations were first observed at six months, and progressed with age. In addition, we found that ERK activation was induced by PKD2 overexpression via B-Raf signaling, providing a possible molecular mechanism of cystogenesis. In PKD2 transgenic mice, B-Raf/MEK/ERK sequential signaling was up-regulated. Additionally, the transgenic human polycystin-2 partially rescues the lethality of Pkd2 knock-out mice and therefore demonstrates that the transgene generated a functional product. Functional strengthening or deregulated activation of PKD2 may be a direct cause of ADPKD. The present study provides evidence for an in vivo role of overexpressed PKD2 in cyst formation. This transgenic mouse model should provide new insights into the pathogenic mechanism of human ADPKD.",
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Park, EY, Sung, YH, Yang, MH, Noh, JY, Park, SY, Lee, TY, Yook, YJ, Yoo, KH, Roh, KJ, Kim, I, Hwang, YH, Oh, GT, Seong, JK, Ahn, C, Lee, HW & Park, JH 2009, 'Cyst formation in kidney via B-raf signaling in the PKD2 transgenic mice', Journal of Biological Chemistry, vol. 284, no. 11, pp. 7214-7222. https://doi.org/10.1074/jbc.M805890200

Cyst formation in kidney via B-raf signaling in the PKD2 transgenic mice. / Park, Eun Young; Sung, Young Hoon; Yang, Moon Hee; Noh, Ji Yeun; Park, So Young; Lee, Tae Young; Yook, Yeon Joo; Yoo, Kyung Hyun; Roh, Kyung Jin; Kim, Ingyu; Hwang, Young Hwan; Oh, Goo Taeg; Seong, Je Kyung; Ahn, Curie; Lee, Han Woong; Park, Jong Hoon.

In: Journal of Biological Chemistry, Vol. 284, No. 11, 13.03.2009, p. 7214-7222.

Research output: Contribution to journalArticle

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T1 - Cyst formation in kidney via B-raf signaling in the PKD2 transgenic mice

AU - Park, Eun Young

AU - Sung, Young Hoon

AU - Yang, Moon Hee

AU - Noh, Ji Yeun

AU - Park, So Young

AU - Lee, Tae Young

AU - Yook, Yeon Joo

AU - Yoo, Kyung Hyun

AU - Roh, Kyung Jin

AU - Kim, Ingyu

AU - Hwang, Young Hwan

AU - Oh, Goo Taeg

AU - Seong, Je Kyung

AU - Ahn, Curie

AU - Lee, Han Woong

AU - Park, Jong Hoon

PY - 2009/3/13

Y1 - 2009/3/13

N2 - The pathogenic mechanisms of human autosomal dominant polycystic kidney disease (ADPKD) have been well known to include the mutational inactivation of PKD2. Although haploinsufficiency and loss of heterozygosity at the Pkd2 locus can cause cyst formation in mice, polycystin-2 is frequently expressed in the renal cyst of human ADPKD, raising the possibility that deregulated activation of PKD2 may be associated with the cystogenesis of human ADPKD. To determine whether increased PKD2 expression is physiologically pathogenic, we generated PKD2-overexpressing transgenic mice. These mice developed typical renal cysts and an increase of proliferation and apoptosis, which are reflective of the human ADPKD phenotype. These manifestations were first observed at six months, and progressed with age. In addition, we found that ERK activation was induced by PKD2 overexpression via B-Raf signaling, providing a possible molecular mechanism of cystogenesis. In PKD2 transgenic mice, B-Raf/MEK/ERK sequential signaling was up-regulated. Additionally, the transgenic human polycystin-2 partially rescues the lethality of Pkd2 knock-out mice and therefore demonstrates that the transgene generated a functional product. Functional strengthening or deregulated activation of PKD2 may be a direct cause of ADPKD. The present study provides evidence for an in vivo role of overexpressed PKD2 in cyst formation. This transgenic mouse model should provide new insights into the pathogenic mechanism of human ADPKD.

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