Aquaporin-1 promotes angiogenesis, fibrosis, and portal hypertension through mechanisms dependent on osmotically sensitive MicroRNAs

Robert C Huebert, Kumaravelu Jagavelu, Helen I. Hendrickson, Meher M. Vasdev, Juan P. Arab, Patrick L. Splinter, Christy E. Trussoni, Nicholas F La Russo, Vijay Shah

Research output: Contribution to journalArticle

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Abstract

Changes in hepatic vasculature accompany fibrogenesis, and targeting angiogenic molecules often attenuates fibrosis in animals. Aquaporin-1 (AQP1) is a water channel, overexpressed in cirrhosis, that promotes angiogenesis by enhancing endothelial invasion. The effect of AQP1 on fibrogenesis in vivo and the mechanisms driving AQP1 expression during cirrhosis remain unclear. The purpose of this study was to test the effect of AQP1 deletion in cirrhosis and explore mechanisms regulating AQP1. After bile duct ligation, wild-type mice overexpress AQP1 that colocalizes with vascular markers and sites of robust angiogenesis. AQP1 knockout mice demonstrated reduced angiogenesis compared with wild-type mice, as evidenced by immunostaining and endothelial invasion/proliferation in vitro. Fibrosis and portal hypertension were attenuated based on immunostaining, portal pressure, and spleen/body weight ratio. AQP1 protein, but not mRNA, was induced by hyperosmolality in vitro, suggesting post-transcriptional regulation. Endothelial cells from normal or cirrhotic mice were screened for microRNA (miR) expression using an array and a quantitative PCR. miR-666 and miR-708 targeted AQP1 mRNA and were decreased in cirrhosis and in cells exposed to hyperosmolality, suggesting that these miRs mediate osmolar changes via AQP1. Binding of the miRs to the untranslated region of AQP1 was assessed using luciferase assays. In conclusion, AQP1 promotes angiogenesis, fibrosis, and portal hypertension after bile duct ligation and is regulated by osmotically sensitive miRs.

Original languageEnglish (US)
Pages (from-to)1851-1860
Number of pages10
JournalAmerican Journal of Pathology
Volume179
Issue number4
DOIs
StatePublished - Oct 2011

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Aquaporin 1
Portal Hypertension
MicroRNAs
Fibrosis
Bile Ducts
Ligation
Untranslated Regions
Portal Pressure
Messenger RNA
Aquaporins
Luciferases
Knockout Mice
Blood Vessels

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Cite this

Aquaporin-1 promotes angiogenesis, fibrosis, and portal hypertension through mechanisms dependent on osmotically sensitive MicroRNAs. / Huebert, Robert C; Jagavelu, Kumaravelu; Hendrickson, Helen I.; Vasdev, Meher M.; Arab, Juan P.; Splinter, Patrick L.; Trussoni, Christy E.; La Russo, Nicholas F; Shah, Vijay.

In: American Journal of Pathology, Vol. 179, No. 4, 10.2011, p. 1851-1860.

Research output: Contribution to journalArticle

Huebert, Robert C ; Jagavelu, Kumaravelu ; Hendrickson, Helen I. ; Vasdev, Meher M. ; Arab, Juan P. ; Splinter, Patrick L. ; Trussoni, Christy E. ; La Russo, Nicholas F ; Shah, Vijay. / Aquaporin-1 promotes angiogenesis, fibrosis, and portal hypertension through mechanisms dependent on osmotically sensitive MicroRNAs. In: American Journal of Pathology. 2011 ; Vol. 179, No. 4. pp. 1851-1860.
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