Activated human peripheral blood neutrophils produce epithelial injury and fibronectin breakdown in vitro

Inflammation ◽  
1992 ◽  
Vol 16 (1) ◽  
pp. 21-30 ◽  
Author(s):  
D. M. Brown ◽  
G. M. Brown ◽  
W. Macnee ◽  
K. Donaldson
2015 ◽  
Vol 159 (1) ◽  
pp. 142-145
Author(s):  
T. V. Polezhaeva ◽  
O. O. Zaitseva ◽  
A. N. Khudyakov ◽  
O. N. Solomina

Blood ◽  
2003 ◽  
Vol 101 (11) ◽  
pp. 4452-4456 ◽  
Author(s):  
Priscilla Biswas ◽  
Barbara Mantelli ◽  
Antonio Sica ◽  
Mauro Malnati ◽  
Carla Panzeri ◽  
...  

Abstract CD4, the primary receptor for entry of HIV, is known to be expressed on T cells and monocytes/macrophages; healthy natural killer (NK) lymphocytes; in vitro human herpesvirus 6 (HHV6)–infected CD8+, NK, and γδ T lymphocytes; CD34+ progenitor cells; and a subset of eosinophils and basophils. We here report the unconventional expression of CD4 at the surface of peripheral blood neutrophils derived from 4 of 51 (7.8%) HIV-1–infected and 3 of 25 (12%) uninfected donors, with similar frequency within the 2 groups. The percentage of CD4+ neutrophils ranged from 39% to 97% of the total neutrophil population. Both surface and cytoplasmic forms of CD4 were present in neutrophils. Quantitative RNA polymerase chain reaction (PCR) revealed that neutrophils contain levels of CD4 mRNA comparable to those of peripheral blood mononuclear cells derived from the same donor. The conformation of CD4 expressed at the surface of neutrophils was similar to that of CD4 expressed on T lymphocytes as determined by the binding of monoclonal antibodies specific for conformational epitopes and the binding of recombinant HIV-1 gp120. Thus, our data provide evidence that neutrophils express endogenous CD4 and bind HIV. Owing to their abundance in peripheral blood, CD4+ neutrophils may influence significantly the biodistribution of HIV delivering it to sites of inflammation or to additional tissue reservoirs.


2000 ◽  
Vol 68 (3) ◽  
pp. 1125-1133 ◽  
Author(s):  
Kiyotaka Yoshiie ◽  
Hyung-Yong Kim ◽  
Jason Mott ◽  
Yasuko Rikihisa

ABSTRACT In patients with human granulocytic ehrlichiosis (HGE), the HGE agent has been seen only in the peripheral blood granulocytes, which have a life span too short for ehrlichial proliferation. To determine if the HGE agent delays the apoptosis of human peripheral blood neutrophils for its advantage, peripheral blood granulocytes consisting mostly of neutrophils were incubated with freshly freed host cell-free HGE agent in vitro. The HGE agent induced a significant delay in morphological apoptosis and the cytoplasmic appearance of histone-associated DNA fragments in the granulocytes. This antiapoptotic effect was dose dependent. Although much weaker than the HGE agent freshly freed from the host cells, noninfectious purified HGE agent stored frozen and thawed also had antiapoptotic effect, which was lost with proteinase K treatment but not with periodate treatment. Treatment of neutrophils with a transglutaminase inhibitor, monodansylcadaverine, blocked the antiapoptotic effect of the HGE agent. Addition of oxytetracycline, however, did not prevent or reverse the antiapoptotic effect of the HGE agent. These results suggest that binding of a protein component(s) of the HGE agent to neutrophils and subsequent cross-linking and/or internalization of the receptor and ehrlichiae are required for antiapoptotic signaling, but ehrlichial protein synthesis and/or proliferation is not required. MG-132, a proteasome inhibitor, and cycloheximide accelerated the apoptosis of neutrophils and overrode the antiapoptotic effect of the HGE agent. Studies with specific inhibitors suggest that protein kinase A, NF-κB, and interleukin 1β are not involved in the antiapoptotic mechanism of the HGE agent.


2003 ◽  
Vol 66 (7) ◽  
pp. 994-995 ◽  
Author(s):  
Erik Larsen ◽  
Arsalan Kharazmi ◽  
Lars P. Christensen ◽  
S. Brøgger Christensen

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