First Author | Simons KH | Year | 2019 |
Journal | J Cell Mol Med | Volume | 23 |
Issue | 6 | Pages | 3888-3896 |
PubMed ID | 30932349 | Mgi Jnum | J:294253 |
Mgi Id | MGI:6454633 | Doi | 10.1111/jcmm.14247 |
Citation | Simons KH, et al. (2019) IRF3 and IRF7 mediate neovascularization via inflammatory cytokines. J Cell Mol Med 23(6):3888-3896 |
abstractText | OBJECTIVE: To elucidate the role of interferon regulatory factor (IRF)3 and IRF7 in neovascularization. METHODS: Unilateral hind limb ischaemia was induced in Irf3(-/-) , Irf7(-/-) and C57BL/6 mice by ligation of the left common femoral artery. Post-ischaemic blood flow recovery in the paw was measured with laser Doppler perfusion imaging. Soleus, adductor and gastrocnemius muscles were harvested to investigate angiogenesis and arteriogenesis and inflammation. RESULTS: Post-ischaemic blood flow recovery was decreased in Irf3(-/-) and Irf7(-/-) mice compared to C57BL/6 mice at all time points up to and including sacrifice, 28 days after surgery (t28). This was supported by a decrease in angiogenesis and arteriogenesis in soleus and adductor muscles of Irf3(-/-) and Irf7(-/-) mice at t28. Furthermore, the number of macrophages around arterioles in adductor muscles was decreased in Irf3(-/-) and Irf7(-/-) mice at t28. In addition, mRNA expression levels of pro-inflammatory cytokines (tnfalpha, il6, ccl2) and growth factor receptor (vegfr2), were decreased in gastrocnemius muscles of Irf3(-/-) and Irf7(-/-) mice compared to C57BL/6 mice. CONCLUSION: Deficiency of IRF3 and IRF7 results in impaired post-ischaemic blood flow recovery caused by attenuated angiogenesis and arteriogenesis linked to a lack of inflammatory components in ischaemic tissue. Therefore, IRF3 and IRF7 are essential regulators of neovascularization. |