CD137‐inducing factors from T cells and macrophages accelerate the destabilization of atherosclerotic plaques in hyperlipidemic mice. Issue 11 (24th July 2014)
- Record Type:
- Journal Article
- Title:
- CD137‐inducing factors from T cells and macrophages accelerate the destabilization of atherosclerotic plaques in hyperlipidemic mice. Issue 11 (24th July 2014)
- Main Title:
- CD137‐inducing factors from T cells and macrophages accelerate the destabilization of atherosclerotic plaques in hyperlipidemic mice
- Authors:
- Jung, In‐Hyuk
Choi, Jae‐Hoon
Jin, Jing
Jeong, Se‐Jin
Jeon, Sejin
Lim, Chaeji
Lee, Mi‐Ran
Yoo, Ji‐Young
Sonn, Seong‐Keun
Kim, Young Ho
Choi, Beom Kyu
Kwon, Byoung S.
Seoh, Ju‐Young
Lee, Cheol Whan
Kim, Dae‐Yong
Oh, Goo Taeg - Abstract:
- Abstract : CD137 (4‐1BB), a member of the tumor necrosis factor receptor superfamily, has been reported to be expressed in atherosclerotic plaques, and to promote lesion formation. However, the role of CD137 in mediating atherosclerotic plaque stability and the possible underlying molecular and cellular mechanisms are poorly understood. Here, apolipoprotein E‐deficient ( ApoE ‐/‐ ) and CD137‐deficient ApoE ‐/‐ ( ApoE ‐/‐ CD137 ‐/‐ ) mice fed a chow diet for 66 wk were used. CD137 induces plaque instability, which is characterized by increased plaque necrosis, decreased collagen content, decreased vascular smooth muscle cell (VSMC) content, and increased macrophage infiltration. CD137 also increases the infiltration of effector T (Teff ) cells into plaque lesion sites, resulting in increased interferon‐γ (IFN‐γ) expression. Interestingly, Teff ‐cell‐derived IFN‐γ inhibits collagen synthesis in atherosclerotic plaques. Furthermore, CD137 activation increases the apoptosis of VSMCs, possibly by decreasing the antiapoptotic regulator, Bcl‐2, and subsequently up‐regulating cleaved caspase‐3. In macrophages, activation of CD137 signaling boosted the oxidized low density lipoprotein‐induced expression of matrix metalloproteinase 9 via the p38 mitogen‐activated protein kinase and extracellular signal‐regulated kinase1/2 signaling pathways. In summary, activation of CD137 signaling decreases the stability of advanced atherosclerotic plaques via its combined effects on Teff cells,Abstract : CD137 (4‐1BB), a member of the tumor necrosis factor receptor superfamily, has been reported to be expressed in atherosclerotic plaques, and to promote lesion formation. However, the role of CD137 in mediating atherosclerotic plaque stability and the possible underlying molecular and cellular mechanisms are poorly understood. Here, apolipoprotein E‐deficient ( ApoE ‐/‐ ) and CD137‐deficient ApoE ‐/‐ ( ApoE ‐/‐ CD137 ‐/‐ ) mice fed a chow diet for 66 wk were used. CD137 induces plaque instability, which is characterized by increased plaque necrosis, decreased collagen content, decreased vascular smooth muscle cell (VSMC) content, and increased macrophage infiltration. CD137 also increases the infiltration of effector T (Teff ) cells into plaque lesion sites, resulting in increased interferon‐γ (IFN‐γ) expression. Interestingly, Teff ‐cell‐derived IFN‐γ inhibits collagen synthesis in atherosclerotic plaques. Furthermore, CD137 activation increases the apoptosis of VSMCs, possibly by decreasing the antiapoptotic regulator, Bcl‐2, and subsequently up‐regulating cleaved caspase‐3. In macrophages, activation of CD137 signaling boosted the oxidized low density lipoprotein‐induced expression of matrix metalloproteinase 9 via the p38 mitogen‐activated protein kinase and extracellular signal‐regulated kinase1/2 signaling pathways. In summary, activation of CD137 signaling decreases the stability of advanced atherosclerotic plaques via its combined effects on Teff cells, VSMCs, and macrophages.—Jung, I.‐H., Choi, J.‐H., Jin, J., Jeong, S.‐J., Jeon, S., Lim, C., Lee, M.‐R., Yoo, J.‐Y., Sonn, S.‐K., Kim, Y. H., Choi, B. K., Kwon, B. S., Seoh, J.‐Y., Lee, C. W., Kim, D.‐Y., Oh, G. T. CD137‐inducing factors from T cells and macrophages accelerate the destabilization of atherosclerotic plaques in hyperlipidemic mice. FASEB J. 28, 4779–4791 (2014). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 28:Issue 11(2014)
- Journal:
- FASEB journal
- Issue:
- Volume 28:Issue 11(2014)
- Issue Display:
- Volume 28, Issue 11 (2014)
- Year:
- 2014
- Volume:
- 28
- Issue:
- 11
- Issue Sort Value:
- 2014-0028-0011-0000
- Page Start:
- 4779
- Page End:
- 4791
- Publication Date:
- 2014-07-24
- Subjects:
- ApoE‐knockout mice -- MMP -- advanced atheroma
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.14-253732 ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13318.xml