TY - JOUR
T1 - Pancreas-specific aquaporin 12 null mice showed increased susceptibility to caerulein-induced acute pancreatitis
AU - Ohta, Eriko
AU - Itoh, Tomohiro
AU - Nemoto, Tomomi
AU - Kumagai, Jiro
AU - Ko, Shigeru B.H.
AU - Ishibashi, Kenichi
AU - Ohno, Mayuko
AU - Uchida, Keiko
AU - Ohta, Akihito
AU - Sohara, Eisei
AU - Uchida, Shinichi
AU - Sasaki, Sei
AU - Rai, Tatemitsu
PY - 2009
Y1 - 2009
N2 - 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) analog, 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.
AB - 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) analog, 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.
KW - Cholecystokinin
KW - Exocytosis
KW - Knockout mouse
KW - Pancreatic acinar cell
KW - Pancreatic exocrine function
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U2 - 10.1152/ajpcell.00117.2009
DO - 10.1152/ajpcell.00117.2009
M3 - Article
C2 - 19726746
AN - SCOPUS:73449112678
SN - 0363-6143
VL - 297
SP - C1368-C1378
JO - American Journal of Physiology - Cell Physiology
JF - American Journal of Physiology - Cell Physiology
IS - 6
ER -