Interleukin 12p40 Deficiency Promotes Abdominal Aortic Aneurysm by Activating CCN2/MMP2 Pathways

J Am Heart Assoc. 2021 Feb 2;10(3):e017633. doi: 10.1161/JAHA.120.017633. Epub 2021 Jan 20.

Abstract

Background Development of abdominal aortic aneurysm (AAA) is associated with proinflammatory cytokines including interleukin-12 (IL12). Deficiency of interleukin 12p40 (IL12p40) increases localized fibrotic events by promoting TGFβ2 (transforming growth factor β)-dependent anti-inflammatory response. Here, we determined whether IL12p40 deficiency in apolipoprotein E-/- mice attenuates the development of AAA by antagonizing proinflammatory response. Methods and Results Double knockout (DKO) mice were generated by crossbreeding IL12p40-/- mice with apolipoprotein E-/- mice (n=12). Aneurysmal studies were performed using angiotensin II (1 µg/kg/min; subcutaneous). Surprisingly, DKO mice did not prevent the development of AAA with angiotensin II infusion. Immunohistological analysis, however, showed distinct pathological features between apolipoprotein E-/- and DKO mice. Polymerase chain reaction (7 day) and cytokine arrays (28 day) of the aortic tissues from DKO mice showed significantly increased expression of cytokines related to anti-inflammatory response (interleukin 5 and interleukin 13), synthetic vascular smooth muscle cell phenotype (Activin receptor-like kinase-1 (ALK-1), artemin, and betacellulin) and T helper 17-associated response (4-1BB, interleukin-17e (Il17e) and Cd40 ligand (Cd-40L)). Indeed, DKO mice exhibited increased expression of the fibro-proteolytic pathway in the medial layer of aortae induced by cellular communication network factor 2 (CCN2) and Cd3+IL17+ cells compared with apolipoprotein E-/- mice. Laser capture microdissection showed predominant expression of CCN2/TGFβ2 in the medial layer of human AAA. Finally, Ccn2 haploinsufficiency in the mice showed decreased AAA incidence in response to elastase infusion, associated with decreased matrix metalloproteinase-2 expression. Conclusions Our study reveals novel roles for IL12p40 deficiency in inducing fibro-proteolytic activities in the aneurysmal mouse model. Mechanistically, these effects of IL12p40 deficiency are mediated by CCN2/matrix metalloproteinase-2 crosstalk in the medial layer of aneurysmal aortae.

Keywords: CCN2; IL12p40; TGFβ2; Th17; abdominal aortic aneurysm.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • Aorta, Abdominal / diagnostic imaging
  • Aorta, Abdominal / metabolism*
  • Aorta, Abdominal / physiopathology
  • Aortic Aneurysm, Abdominal / etiology*
  • Aortic Aneurysm, Abdominal / genetics
  • Aortic Aneurysm, Abdominal / metabolism
  • Blotting, Western
  • Cells, Cultured
  • Connective Tissue Growth Factor / biosynthesis
  • Connective Tissue Growth Factor / genetics*
  • Disease Models, Animal
  • Electrocardiography
  • Female
  • Gene Expression Regulation*
  • Humans
  • Interleukin-12 Subunit p40 / blood
  • Interleukin-12 Subunit p40 / deficiency*
  • Male
  • Matrix Metalloproteinase 2 / biosynthesis
  • Matrix Metalloproteinase 2 / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Middle Aged
  • RNA / genetics*
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / pathology
  • Ultrasonography
  • Vascular Stiffness / physiology

Substances

  • CCN2 protein, mouse
  • Interleukin-12 Subunit p40
  • Connective Tissue Growth Factor
  • RNA
  • Matrix Metalloproteinase 2
  • Mmp2 protein, mouse