Human astrocytes express aquaporin‐1 and aquaporin‐4 in vitro and in vivo

Neuropathology - Tập 27 Số 3 - Trang 245-256 - 2007
Jun‐ichi Satoh1,2, Hiroko Tabunoki1, Takashi Yamamura2, Kunimasa Arima3, Hidehiko Konno4
1Department of Bioinformatics, Meiji Pharmaceutical University,
2Department of Immunology, National Institute of Neuroscience, National Center of Neurology and Psychiatry,
3Department of Neuropathology, National Center Hospital for Mental, Nervous, and Muscular Disorders, National Center of Neurology and Psychiatry, Tokyo and
4Department of Neurology, Nishitaga National Hospital, Sendai, Japan

Tóm tắt

Aquaporins (AQP) constitute an evolutionarily conserved family of integral membrane water transport channel proteins. Previous studies indicate that AQP1 is expressed exclusively in the choroid plexus epithelium, while AQP4 is localized on the vascular foot of astrocytes in the central nervous system (CNS) under physiological conditions. To investigate a role of AQP in the pathophysiology of neurological diseases involving astrogliosis we studied the expression of AQP1 and AQP4 in cultured human astrocytes and brain tissues of multiple sclerosis (MS), cerebral infarction and control cases. By reverse transcriptase‐polymerase chain reaction and western blot analysis, cultured human astrocytes co‐expressed both AQP1 and AQP4 mRNA and proteins, where AQP4 levels were elevated by exposure to interferon‐gamma but neither by tumor necrosis factor‐alpha nor interleukin‐1beta, whereas AQP1 levels were unaffected by any of the cytokines examined. By western blot analysis, AQP1 and AQP4 proteins were detected in the brain homogenates of the MS and non‐MS cases, where both levels were correlated with those of glial fibrillary acid protein. By immunohistochemistry, astrocytes with highly branched processes surrounding blood vessels, along with glial scar, expressed intensely AQP1 and AQP4 in MS and ischemic brain lesions, whereas neither macrophages, neurons nor oligodendrocyte cell bodies were immunopositive. These immunohistochemical results indicate that the expression not only of AQP4 but also of AQP1 was enhanced in MS and ischemic brain lesions located predominantly in astrocytes, suggesting a pivotal role of astrocytic AQP in the maintenance of water homeostasis in the CNS under pathological conditions.

Từ khóa


Tài liệu tham khảo

10.1113/jphysiol.2002.020818

10.1242/jcs.02519

10.1073/pnas.90.15.7275

10.1523/JNEUROSCI.0525-06.2006

10.1056/NEJM200107193450304

10.1073/pnas.022626499

10.1096/fj.04-1711fje

10.1111/j.1471-4159.2005.03111.x

10.1073/pnas.91.26.13052

10.1523/JNEUROSCI.17-01-00171.1997

10.1073/pnas.0437946100

10.1038/72256

10.1074/jbc.M413627200

10.1152/ajpcell.00298.2003

10.1007/s00401-003-0709-y

10.1007/s00401-005-1052-2

10.1084/jem.20050304

10.1097/00001756-200402090-00009

10.1073/pnas.0409308102

10.1097/00004647-200105000-00001

10.1016/S0002-9440(10)63322-6

10.1046/j.1365-2990.2002.00375.x

10.1021/bi00007a015

10.1016/j.nbd.2005.05.021

10.1007/978-3-7091-0651-8_101

10.1007/3-211-30714-1_82

RodríguezA Pérez‐GraciaE EspinosaJC PumarolaM TorresJM FerrerI.Increased expression of water channel aquaporin 1 and aquaporin 4 in Creutzfeldt‐Jakob disease and in bovine spongiform encephalopathy‐infected bovine‐PrP transgenic mice.Acta Neuropathol2006;112:573–85.

10.1038/sj.bjc.6600512

10.1136/jnnp.72.2.262

10.1227/01.NEU.0000148904.57841.6B

10.1038/nature03460

10.2353/ajpath.2006.050596

HuJ VerkmanAS.Increased migration and metastatic potential of tumor cells expressing aquaporin water channels.FASEB J2006;20:1892–4.

10.1242/jcs.02680

10.1152/ajpcell.00180.2003

10.1074/jbc.C100646200

10.1074/jbc.272.20.12984

10.1016/j.neulet.2005.10.060

10.1111/j.1460-9568.2006.04829.x

10.1096/fj.04-1901hyp

10.1172/JCI118659

10.1097/01.ASN.0000053420.37216.9E

10.1074/jbc.M209980200

10.1016/S0169-328X(01)00254-6

10.1002/jnr.10603

10.1016/S0169-328X(01)00067-5

Smith JK, 1999, Interferon‐alpha upregulates gene expression of aquaporin‐5 in human parotid glands, J Interferon Cytokine Res, 19, 929, 10.1089/107999099313479

10.1074/jbc.270.39.22907

10.1016/S0306-4522(99)00182-7

10.1002/glia.20256

10.1016/j.neulet.2005.06.046

10.1002/cne.20589