首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Suppression of ERK activation in urethral epithelial cells infected with Neisseria gonorrhoeae and its isogenic minD mutant contributes to anti-apoptosis
Institution:1. Molecular Oncology GRP and Viral Pathology — IC, Portuguese Institute of Oncology of Porto (IPO Porto), Porto, Portugal;2. Faculty of Medicine, University of Porto, Porto, Portugal;3. FP-ENAS Research Unit, UFP Energy, Environment and Health Research Unit, CEBIMED, Biomedical Research centre, Fernando Pessoa University, Porto, Portugal;4. LPCC, Research Department, Portuguese League Against Cancer (LPPC-NRN), Portugal;1. Department of Medical Laboratory Science, Faculty of Health Sciences, Hokkaido University, Sapporo, Japan;2. Division of Biomedical Imaging Research, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan
Abstract:In gonococci-infected transduced human urethral epithelial cells (THUEC), the role of ERK, a mitogen-activated protein kinase (MAPK), in apoptosis is unknown. We observed lowering of ERK activation in THUEC following infection with anti-apoptosis-inducing Neisseria gonorrhoeae strain CH811. An isogenic cell division mutant of this strain, Ng CJSD1 (minD deficient), which is large and abnormally shaped, reduced ERK phosphorylation levels even more than its parental strain in THUEC. This led to higher anti-apoptosis in mutant-infected cells as compared to the parental strain-infected cells. Our results suggest that N. gonorrhoeae infection reduces ERK activation in THUEC contributing to anti-apoptosis.
Keywords:Anti-apoptosis  Urethral epithelial cells  ERK regulation  ERK"}  {"#name":"keyword"  "$":{"id":"kwrd0040"}  "$$":[{"#name":"text"  "_":"extracellular signal – regulated kinase  GCMBK"}  {"#name":"keyword"  "$":{"id":"kwrd0050"}  "$$":[{"#name":"text"  "_":"gonococcal medium base + Kellogg's supplement  THUEC"}  {"#name":"keyword"  "$":{"id":"kwrd0060"}  "$$":[{"#name":"text"  "_":"transduced human urethral epithelial cells
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号