scholarly journals Apoptosis induction in gastric mucous cells in vitro: lesser potency of Helicobacter pylori than Escherichia coli lipopolysaccharide, but positive interaction with ibuprofen

2006 ◽  
Vol 12 (1) ◽  
pp. 47-56 ◽  
Author(s):  
Emma Durkin ◽  
Anthony P. Moran ◽  
Peter J. Hanson
2001 ◽  
Vol 120 (5) ◽  
pp. A708-A709
Author(s):  
T KANEKO ◽  
H OTA ◽  
M HAYAMA ◽  
K NAKAJIMA ◽  
A YOSHIZAWA ◽  
...  

Helicobacter ◽  
2004 ◽  
Vol 9 (4) ◽  
pp. 302-312 ◽  
Author(s):  
Tetsufumi Takahashi ◽  
Tsukasa Matsumoto ◽  
Masahiko Nakamura ◽  
Hidenori Matsui ◽  
Hiroaki Kiyohara ◽  
...  

2000 ◽  
Vol 437 (5) ◽  
pp. 514-520 ◽  
Author(s):  
Taimei Kaneko ◽  
Hiroyoshi Ota ◽  
Masayoshi Hayama ◽  
Taiji Akamatsu ◽  
Tsutomu Katsuyama

Helicobacter ◽  
2003 ◽  
Vol 8 (5) ◽  
pp. 513-520 ◽  
Author(s):  
Geoff V. Smith ◽  
Anthony P. Moran ◽  
Mona Bajaj-Elliott ◽  
Michael J.G. Farthing

1972 ◽  
Vol 135 (4) ◽  
pp. 850-859 ◽  
Author(s):  
Olof Sjöberg

The breaking of tolerance against the lipopolysaccharide from E. coli 055:B5 was studied. It was found that immune responsiveness recovered very slowly in vivo, tolerance still existing 3 wk after the last tolerizing injection. However, if spleen cells from tolerant mice were transferred into irradiated syngeneic recipients, the tolerant state was readily broken. Spleen cells transferred 3 days after the last tolerance-maintaining dose did not respond, whereas cells transferred on day 5 or 7 responded equally well as normal spleen cells. It was also possible to break tolerance by incubating tolerant spleen cells, which did not respond after transfer, for 20 hr in vitro before transfer into irradiated recipients. The results suggest that there exist reversibly inactivated cells in tolerant animals and that these cells can be reactivated upon removal of the cells to a neutral environment.


2005 ◽  
Vol 389 (2) ◽  
pp. 541-548 ◽  
Author(s):  
Rajesh K. Soni ◽  
Parul Mehra ◽  
Gauranga Mukhopadhyay ◽  
Suman Kumar Dhar

In Escherichia coli, DnaC is essential for loading DnaB helicase at oriC (the origin of chromosomal DNA replication). The question arises as to whether this model can be generalized to other species, since many eubacterial species fail to possess dnaC in their genomes. Previously, we have reported the characterization of HpDnaB (Helicobacter pylori DnaB) both in vitro and in vivo. Interestingly, H. pylori does not have a DnaC homologue. Using two different E. coli dnaC (EcdnaC) temperature-sensitive mutant strains, we report here the complementation of EcDnaC function by HpDnaB in vivo. These observations strongly suggest that HpDnaB can bypass EcDnaC activity in vivo.


2001 ◽  
Vol 120 (5) ◽  
pp. A708-A709
Author(s):  
Taimei Kaneko ◽  
Hiroyoshi Ota ◽  
Masayoshi Hayama ◽  
Kosei Nakajima ◽  
Akihiko Yoshizawa ◽  
...  

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