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Functional Roles of p38 Mitogen-Activated Protein Kinase in Macrophage-Mediated Inflammatory Responses

Yanyan YangDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Republic of KoreaSeung Cheol KimDivision of Gynecologic Oncology Department of Obstetrics and Gynecology, Ewha Womans University Mokdong Hospital College of Medicine, Ewha Womans University, Seoul 158-710, Republic of KoreaTao YuDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Republic of KoreaYoung‐Su YiDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Republic of KoreaMan Hee RheeCollege of Veterinary Medicine, Kyungpook National University, Daegu 702-701, Republic of KoreaGi-Ho SungDepartment of Herbal Crop Research, National Institutes of Horticultural & Herbal Science, Rural Development Administration, Suwon 441-707, Republic of KoreaByong Chul YooColorectal Cancer Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi 410-769, Republic of KoreaJae Youl ChoDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Republic of Korea
2014en
ABI

Аннотация

Inflammation is a natural host defensive process that is largely regulated by macrophages during the innate immune response. Mitogen-activated protein kinases (MAPKs) are proline-directed serine and threonine protein kinases that regulate many physiological and pathophysiological cell responses. p38 MAPKs are key MAPKs involved in the production of inflammatory mediators, including tumor necrosis factor-α (TNF-α) and cyclooxygenase-2 (COX-2). p38 MAPK signaling plays an essential role in regulating cellular processes, especially inflammation. In this paper, we summarize the characteristics of p38 signaling in macrophage-mediated inflammation. In addition, we discuss the potential of using inhibitors targeting p38 expression in macrophages to treat inflammatory diseases.

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