Am J Physiol Cell Physiol AJP: Renal Physiology
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Am J Physiol Cell Physiol (September 2, 2009). doi:10.1152/ajpcell.00117.2009
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Submitted on March 13, 2009
Revised on August 18, 2009
Accepted on September 1, 2009

Pancreas-specific aquaporin 12 null mice showed increased susceptibility to caerulein-induced acute pancreatitis

Eriko Ohta1, Tomohiro Itoh1, Tomomi Nemoto2, Jiro Kumagai1, Shigeru BH Ko3, Kenichi Ishibashi4, Mayuko Ohno5, Keiko Uchida5, Akihito Ohta1, Eisei Sohara1, Shinichi Uchida6, Sei Sasaki1, and Tatemitsu Rai1*

1 Tokyo Medical and Dental University
2 National Institute for Physiological Sciences and JST, CREST
3 Nagoya University Graduate School of Medicine
4 Meiji Pharmaceutical University
5 Tokyo Women's Medical University
6 Graduate School of Medicine, Tokyo Medical and Dental University

* To whom correspondence should be addressed. E-mail: trai.kid{at}tmd.ac.jp.

Aquaporin 12 (AQP12) is the most recently identified member of the mammalian AQP family and is specifically expressed in pancreatic acinar cells. In vitro expression studies have revealed that AQP12 is localized at intracellular sites. To determine the physiological roles of AQP12 in the pancreas we generated knockout mice for this gene (AQP12-KO). No obvious differences were observed under normal conditions between wild-type (WT) and AQP12-KO mice in terms of growth, blood chemistry, pancreatic fluid content, or histology. However, when we induced pancreatitis through the administration of a cholecystokinin-8 (CCK-8) analogue, the AQP12-KO mice showed more severe pathological damage to this organ than WT mice. Furthermore, when we analyzed exocytosis in the pancreatic acini using a two-photon excitation imaging method, the results revealed larger exocytotic vesicles (vacuoles) in the acini of AQP12-KO mice at a high CCK-8 dose (100 nM). From these results, we conclude that AQP12 may function in the mechanisms that control the proper secretion of pancreatic fluid following rapid and intense stimulation.







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