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   Fcγ receptor i alpha chain (CD64) expression in macrophages is critical for the onset of meningitis by Escherichia coli K1  
   
نویسنده mittal r. ,sukumaran s.k. ,selvaraj s.k. ,wooster d.g. ,madan babu m. ,schreiber a.d. ,sjef verbeek j. ,prasadarao n.v.
منبع plos pathogens - 2010 - دوره : 6 - شماره : 11
چکیده    Neonatal meningitis due to escherichia coli k1 is a serious illness with unchanged morbidity and mortality rates for the last few decades. the lack of a comprehensive understanding of the mechanisms involved in the development of meningitis contributes to this poor outcome. here,we demonstrate that depletion of macrophages in newborn mice renders the animals resistant to e. coli k1 induced meningitis. the entry of e. coli k1 into macrophages requires the interaction of outer membrane protein a (ompa) of e. coli k1 with the alpha chain of fcγ receptor i (fcγria,cd64) for which igg opsonization is not necessary. overexpression of full-length but not c-terminal truncated fccria in cos-1 cells permits e. coli k1 to enter the cells. moreover,ompa binding to fcγria prevents the recruitment of the γ-chain and induces a different pattern of tyrosine phosphorylation of macrophage proteins compared to igg2a induced phosphorylation. of note,fcγria-/- mice are resistant to e. coli infection due to accelerated clearance of bacteria from circulation,which in turn was the result of increased expression of cr3 on macrophages. reintroduction of human fccria in mouse fcγria-/- macrophages in vitro increased bacterial survival by suppressing the expression of cr3. adoptive transfer of wild type macrophages into fcγria-/- mice restored susceptibility to e. coli infection. together,these results show that the interaction of fcγri alpha chain with ompa plays a key role in the development of neonatal meningitis by e. coli k1. © 2010 mittal et al.
آدرس division of infectious diseases,the saban research institute,childrens hospital los angeles,los angeles,ca, United States, division of infectious diseases,the saban research institute,childrens hospital los angeles,los angeles,ca, United States, division of infectious diseases,the saban research institute,childrens hospital los angeles,los angeles,ca, United States, division of infectious diseases,the saban research institute,childrens hospital los angeles,los angeles,ca, United States, structural studies division,medical research council,laboratory of molecular biology,cambridge, United Kingdom, hematology and oncology division,university of pennsylvania school of medicine,philadelphia,pa, United States, department of human genetics,university medical center,leiden, Netherlands, division of infectious diseases,the saban research institute,childrens hospital los angeles,los angeles,ca,united states,keck school of medicine,university of southern california,los angeles,ca, United States
 
     
   
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