Interactions of gut epithelial barrier, microbiome and p53 family members – what is their impact on liver cirrhosis?

2018 ◽  
Vol 56 (01) ◽  
pp. E2-E89 ◽  
Author(s):  
L Wächter ◽  
M Haderer ◽  
E Aschenbrenner ◽  
K Pollinger ◽  
S Schlosser ◽  
...  
2013 ◽  
Vol 33 (10) ◽  
pp. 1457-1469 ◽  
Author(s):  
Kirsten E. Pijls ◽  
Daisy M. A. E. Jonkers ◽  
Elhaseen E. Elamin ◽  
Ad A. M. Masclee ◽  
Ger H. Koek

eLife ◽  
2022 ◽  
Vol 11 ◽  
Author(s):  
Ananya Chakravarti ◽  
Heshani N Thirimanne ◽  
Savanna Brown ◽  
Brian R Calvi

p53 gene family members in humans and other organisms encode a large number of protein isoforms whose functions are largely undefined. Using Drosophila as a model, we find that a p53B isoform is expressed predominantly in the germline where it colocalizes with p53A into subnuclear bodies. It is only p53A, however, that mediates the apoptotic response to ionizing radiation in the germline and soma. In contrast, p53A and p53B are both required for the normal repair of meiotic DNA breaks, an activity that is more crucial when meiotic recombination is defective. We find that in oocytes with persistent DNA breaks p53A is also required to activate a meiotic pachytene checkpoint. Our findings indicate that Drosophila p53 isoforms have DNA lesion and cell type-specific functions, with parallels to the functions of mammalian p53 family members in the genotoxic stress response and oocyte quality control.


FEBS Letters ◽  
2002 ◽  
Vol 525 (1-3) ◽  
pp. 93-99 ◽  
Author(s):  
Sebastian Dietz ◽  
Karen Rother ◽  
Casimir Bamberger ◽  
Hartwig Schmale ◽  
Joachim Mössner ◽  
...  

Oncogene ◽  
2005 ◽  
Vol 24 (49) ◽  
pp. 7273-7280 ◽  
Author(s):  
Giulia Fontemaggi ◽  
Aymone Gurtner ◽  
Alexander Damalas ◽  
Antonio Costanzo ◽  
Yujiro Higashi ◽  
...  
Keyword(s):  

BMC Genomics ◽  
2010 ◽  
Vol 11 (Suppl 1) ◽  
pp. S5 ◽  
Author(s):  
Jagadeesh N Mavinahalli ◽  
Arumugam Madhumalar ◽  
Roger W Beuerman ◽  
David P Lane ◽  
Chandra Verma

2016 ◽  
Vol 310 (11) ◽  
pp. G962-G972 ◽  
Author(s):  
Jin-Hang Gao ◽  
Shi-Lei Wen ◽  
Huan Tong ◽  
Chun-Hui Wang ◽  
Wen-Juan Yang ◽  
...  

Inflammatory transport through the gut-liver axis may facilitate liver cirrhosis. Cyclooxygenase-2 (COX-2) has been considered as one of the important molecules that regulates intestinal epithelial barrier function. This study was aimed to test the hypothesis that inhibition of COX-2 by celecoxib might alleviate liver cirrhosis via reduction of intestinal inflammatory transport in thiacetamide (TAA) rat model. COX-2/prostaglandin E2 (PGE2)/EP-2/p-ERK integrated signal pathways regulated the expressions of intestinal zonula occludens-1 (ZO-1) and E-cadherin, which maintain the function of intestinal epithelial barrier. Celecoxib not only decreased the intestinal permeability to a 4-kDa FITC-dextran but also significantly increased expressions of ZO-1 and E-cadherin. When celecoxib greatly decreased intestinal levels of LPS, TNF-α, and IL-6, it significantly enhanced T cell subsets reduced by TAA. As a result, liver fibrosis induced by TAA was significantly alleviated in the celecoxib group. These data indicated that celecoxib improved the integrity of intestinal epithelial barrier, blocked inflammatory transport through the dysfunctional gut-liver axis, and ameliorated the progress of liver cirrhosis.


PLoS ONE ◽  
2013 ◽  
Vol 8 (7) ◽  
pp. e69152 ◽  
Author(s):  
Ivan Raimondi ◽  
Yari Ciribilli ◽  
Paola Monti ◽  
Alessandra Bisio ◽  
Loredano Pollegioni ◽  
...  

Cell Cycle ◽  
2011 ◽  
Vol 10 (24) ◽  
pp. 4272-4279 ◽  
Author(s):  
David P. Lane ◽  
Arumugam Madhumalar ◽  
Alison P. Lee ◽  
Boon-Hui Tay ◽  
Chandra Verma ◽  
...  

2021 ◽  
pp. 1-16
Author(s):  
Sumiran Kumar Gurung ◽  
Lokesh Nigam ◽  
Kunwar Somesh Vikramdeo ◽  
Neelima Mondal

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