4.5 Article

C1qTNF-related protein-6 increases the expression of interleukin-10 in macrophages

期刊

MOLECULES AND CELLS
卷 30, 期 1, 页码 59-64

出版社

KOREAN SOC MOLECULAR & CELLULAR BIOLOGY
DOI: 10.1007/s10059-010-0088-x

关键词

C1qTNF6; CTRP6; ERK1/2; interleukin-10; macrophages

资金

  1. Ministry of Health and Welfare, Republic of Korea [A080151]
  2. Korean Government [KRF-2008-331-C00184]
  3. Ministry of Knowledge Economy [RTI04-01-01]
  4. Ministry of Education, Science and Technology, Republic of Korea [M108KM010008-08K1301-00810]
  5. Ministry of Health and Welfare, Korea [00-PJ3-PG6-GN070001]
  6. Korea Health Promotion Institute [A080151] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

C1qTNF-Related proteins (CTRPs), a new highly conserved family of adiponectin paralogs, were recently identified as being involved in diverse processes including metabolism, host defense, apoptosis, cell differentiation, and organogenesis. However, the functional role of CTRP6 remains poorly identified. Here we provide evidence that CTRP6 induces the expression of interleukin-10 (IL-10) in macrophages. Conditioned medium from CTRP6-expressing HEK293 cells increased IL-10 expression in Raw264.7 cells. The globular domain of CTRP6 (gCTRP6) also dose-dependently increased both IL-10 mRNA and protein expression levels, with transcript levels increasing within 2 h. Furthermore, the globular domain of CTRP6 rapidly induced phosphorylation of ERK1/2 in Raw264.7 cells. Treatment with U0126, a selective inhibitor, abolished CTRP6-stimulated IL-10 induction. Taken together, there results demonstrate that CTRP6 induces expression of IL-10 via ERK1/2 activation. Considering that IL-10 is a potent anti-inflammatory cytokine that modulates inflammatory signaling pathways, CTRP6 may be a novel target for pharmacological drugs in inflammatory diseases.

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