Chemotactic Activity of Collagen-Like Polypeptides for Human Peripheral Blood Neutrophils

1986 ◽  
Vol 39 (3) ◽  
pp. 255-266 ◽  
Author(s):  
Debra L. Laskin ◽  
Terutoshi Kimura ◽  
Shumpei Sakakibara ◽  
David J. Riley ◽  
Richard A. Berg
Keyword(s):  
Peripheral Blood ◽  
Human Peripheral Blood ◽  
Chemotactic Activity ◽  
Blood Neutrophils

Mevalonate-Dependent Inhibition of Transendothelial Migration and Chemotaxis of Human Peripheral Blood Neutrophils by Pravastatin

1997 ◽  
Vol 81 (6) ◽  
pp. 963-969 ◽  
Author(s):  
Stefan Dunzendorfer ◽  
Dorothea Rothbucher ◽  
Peter Schratzberger ◽  
Norbert Reinisch ◽  
Christian M. Kähler ◽  
...  
Keyword(s):  
Peripheral Blood ◽  
Human Peripheral Blood ◽  
Transendothelial Migration ◽  
Dependent Inhibition ◽  
Blood Neutrophils

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
Keyword(s):  
Peripheral Blood ◽  
Human Peripheral Blood ◽  
Epithelial Injury ◽  
Blood Neutrophils

scholarly journals Production of Macrophage Inflammatory Protein 3α (MIP-3α) (CCL20) and MIP-3β (CCL19) by Human Peripheral Blood Neutrophils in Response to Microbial Pathogens

2003 ◽  
Vol 71 (1) ◽  
pp. 524-526 ◽  
Author(s):  
Tohru Akahoshi ◽  
Takeshi Sasahara ◽  
Rie Namai ◽  
Toshimichi Matsui ◽  
Hiroyuki Watabe ◽  
...  
Keyword(s):  
Immune Responses ◽  
Peripheral Blood ◽  
Human Peripheral Blood ◽  
Microbial Pathogens ◽  
T Cell Subsets ◽  
Gram Negative Bacteria ◽  
Gram Negative ◽  
Inflammatory Protein ◽  
Blood Neutrophils ◽  
Macrophage Inflammatory Protein

ABSTRACT Effects of bacterial pathogens on the production of macrophage inflammatory protein 3α (MIP-3α) and MIP-3β from human peripheral blood neutrophils were investigated. Neutrophils produced both chemokines by coincubation with either gram-positive or gram-negative bacteria. Neutrophils may initiate antigen-specific immune responses through the release of these chemokines that are capable of promoting selective recruitment of dendritic cells and T-cell subsets.

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