Wataru Nishimura

Dr. Wataru Nishimura

IUWH School of Medicine, Narita, Chiba, Japan
orcid

Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2006 in Developmental Biology
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Journal Article
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Wataru NishimuraWataru Nishimura
Wataru Nishimura
TKTakuma Kondo
Takuma Kondo
TSTherese Salameh
Therese Salameh
IKIlham El Khattabi
Ilham El Khattabi
RDRikke Dodge
Rikke Dodge
ASArun Sharma
Arun Sharma

1 June 2003 in Molecular and Cellular Biology
Verified
Journal Article
Open access
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SHSusumu Hirabayashi
Susumu Hirabayashi
MTMakiko Tajima
Makiko Tajima
IYIkuko Yao
Ikuko Yao
Wataru NishimuraWataru Nishimura
Wataru Nishimura
HMHiroki Mori
Hiroki Mori
YHYutaka Hata
Yutaka Hata
MAGI-1 is a membrane-associated guanylate kinase protein at tight junctions in epithelial cells. It interacts with various molecules and functions as a scaffold protein at cell junctions. We report here a novel MAGI-1-binding protein that we named junctional adhesion molecule 4 (JAM4). JAM4 belongs to an immunoglobulin protein family. JAM4 was colocalized with ZO-1 in kidney glomeruli and in intestinal epithelial cells. Biochemical in vitro studies revealed that JAM4 bound to MAGI-1 but not to ZO-1, whereas JAM1 did not bind to MAGI-1. JAM4 and MAGI-1 interacted with each other and formed clusters in COS-7 cells when coexpressed. JAM4 mediated calcium-independent homophilic adhesion and was accumulated at cell-cell contacts when expressed in L cells. MAGI-1, ZO-1, and occludin were recruited to JAM4-based cell contacts. JAM4 also reduced the permeability of CHO cell monolayers. MAGI-1 strengthened JAM4-mediated cell adhesion in L cells and sealing effects in CHO cells. These findings suggest that JAM4 together with MAGI-1 provides an adhesion machinery at tight junctions, which may regulate the permeability of kidney glomerulus and small intestinal epithelial cells.

13 December 2014 in Diabetologia
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Wataru NishimuraWataru Nishimura
Wataru Nishimura
STSatoru Takahashi
Satoru Takahashi
KYKazuki Yasuda
Kazuki Yasuda

15 August 2010 in Journal of Cell Science
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Journal Article
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WLWan-Chun Li
Wan-Chun Li
JRJ. Michael Rukstalis
J. Michael Rukstalis
Wataru NishimuraWataru Nishimura
Wataru Nishimura
VTVaja Tchipashvili
Vaja Tchipashvili
JHJoel F. Habener
Joel F. Habener
SBSusan Bonner-Weir
Susan Bonner-Weir
The adult pancreas has considerable capacity to regenerate in response to injury. We hypothesized that after partial pancreatectomy (Px) in adult rats, pancreatic-duct cells serve as a source of regeneration by undergoing a reproducible dedifferentiation and redifferentiation. We support this hypothesis by the detection of an early loss of the ductal differentiation marker Hnf6 in the mature ducts, followed by the transient appearance of areas composed of proliferating ductules, called foci of regeneration, which subsequently form new pancreatic lobes. In young foci, ductules express markers of the embryonic pancreatic epithelium – Pdx1, Tcf2 and Sox9 – suggesting that these cells act as progenitors of the regenerating pancreas. The endocrine-lineage-specific transcription factor Neurogenin3, which is found in the developing embryonic pancreas, was transiently detected in the foci. Islets in foci initially resemble embryonic islets in their lack of MafA expression and lower percentage of β-cells, but with increasing maturation have increasing numbers of MafA+ insulin+ cells. Taken together, we provide a mechanism by which adult pancreatic duct cells recapitulate aspects of embryonic pancreas differentiation in response to injury, and contribute to regeneration of the pancreas. This mechanism of regeneration relies mainly on the plasticity of the differentiated cells within the pancreas.

23 December 2007 in Developmental Biology
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Journal Article
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Wataru NishimuraWataru Nishimura
Wataru Nishimura
SRSheldon Rowan
Sheldon Rowan
TSTherese Salameh
Therese Salameh
RMRichard L. Maas
Richard L. Maas
SBSusan Bonner-Weir
Susan Bonner-Weir
ASArun Sharma
Arun Sharma

22 June 2015 in Proceedings of the National Academy of Sciences
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SAShun-Ichiro Asahara
Shun-Ichiro Asahara
HEHiroaki Etoh
Hiroaki Etoh
HIHiroyuki Inoue
Hiroyuki Inoue
KTKyoko Teruyama
Kyoko Teruyama
YSYuki Shibutani
Yuki Shibutani
YKYoshiaki Kido
Yoshiaki Kido
Significance: Recently, the potassium voltage-gated channel, KQT-like subfamily Q, member1 ( KCNQ1 ) gene has received much attention as a candidate susceptibility gene for type 2 diabetes in Asian, European, and other populations. The molecular mechanism underlying the association of KCNQ1 with the onset of type 2 diabetes has remained unclear; however, we have now found that a paternal allelic mutation of Kcnq1 results in the up-regulation of the neighboring imprinted gene cyclin-dependent kinase inhibitor 1C ( Cdkn1c ), a cell cycle inhibitor, in pancreatic β-cells of mice, with this effect being mediated by epigenetic modification of the Cdkn1c promoter. These changes seem to be responsible for the reduced pancreatic β-cell mass and impaired glucose tolerance characteristics of Kcnq1 mutant mice.