Unknown

Dataset Information

0

CXCR2: From Bench to Bedside.


ABSTRACT: Leukocyte recruitment to sites of infection or tissue damage plays a crucial role for the innate immune response. Chemokine-dependent signaling in immune cells is a very important mechanism leading to integrin activation and leukocyte recruitment. CXC chemokine receptor 2 (CXCR2) is a prominent chemokine receptor on neutrophils. During the last years, several studies were performed investigating the role of CXCR2 in different diseases. Until now, many CXCR2 inhibitors are tested in animal models and clinical trials and promising results were obtained. This review gives an overview of the structure of CXCR2 and the signaling pathways that are activated following CXCR2 stimulation. We discuss in detail the role of this chemokine receptor in different disease models including acute lung injury, COPD, sepsis, and ischemia-reperfusion-injury. Furthermore, this review summarizes the results of clinical trials which used CXCR2 inhibitors.

SUBMITTER: Stadtmann A 

PROVIDER: S-EPMC3426767 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

altmetric image

Publications

CXCR2: From Bench to Bedside.

Stadtmann Anika A   Zarbock Alexander A  

Frontiers in immunology 20120824


Leukocyte recruitment to sites of infection or tissue damage plays a crucial role for the innate immune response. Chemokine-dependent signaling in immune cells is a very important mechanism leading to integrin activation and leukocyte recruitment. CXC chemokine receptor 2 (CXCR2) is a prominent chemokine receptor on neutrophils. During the last years, several studies were performed investigating the role of CXCR2 in different diseases. Until now, many CXCR2 inhibitors are tested in animal models  ...[more]

Similar Datasets

2006-08-29 | GSE5663 | GEO
| S-EPMC4498442 | biostudies-other
| S-EPMC4018312 | biostudies-literature
| S-EPMC7717128 | biostudies-literature
| S-EPMC6735664 | biostudies-literature
| S-EPMC5983582 | biostudies-literature
| S-EPMC4791785 | biostudies-literature
| S-EPMC4011589 | biostudies-literature
| S-EPMC7670077 | biostudies-literature
| S-EPMC8662562 | biostudies-literature