TY - JOUR
T1 - Sex differences in coxsackievirus B3-induced myocarditis
T2 - IL-12Rβ1 signaling and IFN-γ increase inflammation in males independent from STAT4
AU - Frisancho-Kiss, Sylvia
AU - Nyland, Jennifer F.
AU - Davis, Sarah E.
AU - Augusto Frisancho, J.
AU - Barrett, Masheka A.
AU - Rose, Noel R.
AU - Fairweather, De Lisa
N1 - Funding Information:
This work was supported by National Institutes of Health Grants HL67290, HL70729, AI51835, ES03819 and T32 ES07141 (to J.F.N.).
PY - 2006/12/18
Y1 - 2006/12/18
N2 - Cardiovascular disease is the number one killer of men and women in North America. Male BALB/c mice infected with coxsackievirus B3 (CVB3) develop more severe inflammatory heart disease compared to female mice, similar to the increased heart disease that occurs in men. We show here that increased inflammation in male mice is not due to increased viral replication in the heart, but associated with increased proinflammatory cytokines IL-1β, IL-18 and IFN-γ. We have previously reported that IL-12Rβ1 signaling increases CVB3-induced myocarditis and IL-1β/IL-18 levels in males, while IL-12(p35)/STAT4-induced IFN-γ does not alter the severity of acute disease. However, whether differences exist between males and females in these two cytokine signaling pathways is unknown. In this study, we examined sex differences in 1) IL-12Rβ1 signaling or 2) STAT4/IFN-γ pathways following CVB3 infection in BALB/c mice. We found that male and female mice deficient in IL-12Rβ1 had decreased inflammation and viral replication in the heart, indicating that IL-12Rβ1 signaling increases myocarditis in both sexes. In contrast, STAT4 deficiency did not alter the sex difference in myocarditis, with males maintaining increased inflammation over females. IFN-γ deficient males, however, had decreased myocarditis and viral replication compared to females. Thus, IFN-γ increases inflammation in males independent from STAT4. These results demonstrate that sex differences greatly influence viral replication and the severity of acute CVB3-induced myocarditis.
AB - Cardiovascular disease is the number one killer of men and women in North America. Male BALB/c mice infected with coxsackievirus B3 (CVB3) develop more severe inflammatory heart disease compared to female mice, similar to the increased heart disease that occurs in men. We show here that increased inflammation in male mice is not due to increased viral replication in the heart, but associated with increased proinflammatory cytokines IL-1β, IL-18 and IFN-γ. We have previously reported that IL-12Rβ1 signaling increases CVB3-induced myocarditis and IL-1β/IL-18 levels in males, while IL-12(p35)/STAT4-induced IFN-γ does not alter the severity of acute disease. However, whether differences exist between males and females in these two cytokine signaling pathways is unknown. In this study, we examined sex differences in 1) IL-12Rβ1 signaling or 2) STAT4/IFN-γ pathways following CVB3 infection in BALB/c mice. We found that male and female mice deficient in IL-12Rβ1 had decreased inflammation and viral replication in the heart, indicating that IL-12Rβ1 signaling increases myocarditis in both sexes. In contrast, STAT4 deficiency did not alter the sex difference in myocarditis, with males maintaining increased inflammation over females. IFN-γ deficient males, however, had decreased myocarditis and viral replication compared to females. Thus, IFN-γ increases inflammation in males independent from STAT4. These results demonstrate that sex differences greatly influence viral replication and the severity of acute CVB3-induced myocarditis.
KW - Cytokine
KW - Heart disease
KW - Inflammation
KW - Sex
KW - Virus
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U2 - 10.1016/j.brainres.2006.08.003
DO - 10.1016/j.brainres.2006.08.003
M3 - Article
C2 - 16949558
AN - SCOPUS:33845334207
SN - 0006-8993
VL - 1126
SP - 139
EP - 147
JO - Brain Research
JF - Brain Research
IS - 1
ER -