PMID- 21803942 OWN - NLM STAT- MEDLINE DCOM- 20111122 LR - 20200930 IS - 1522-1539 (Electronic) IS - 0363-6135 (Linking) VI - 301 IP - 4 DP - 2011 Oct TI - Sex hormone control of left ventricular structure/function: mechanistic insights using echocardiography, expression, and DNA methylation analyses in adult mice. PG - H1706-15 LID - 10.1152/ajpheart.00088.2011 [doi] AB - Calcium flux into and out of the sarco(endo)plasmic reticulum is vitally important to cardiac function because the cycle of calcium entry and exit controls contraction and relaxation. Putative estrogen and androgen consensus binding sites near to a CpG island are present in the cardiac calsequestrin 2 (CSQ2) promoter. Cardiomyocytes express sex hormone receptors and respond to sex hormones. We hypothesized that sex hormones control CSQ2 expression in cardiomyocytes and so affect cardiac structure/function. Echocardiographic analysis of male and female C57bl6n mice identified thinner walled and lighter hearts in females and significant concentric remodeling after long-term gonadectomy. CSQ2 and sodium-calcium exchanger-1 (NCX1) expression was significantly increased in female compared with male hearts and decreased postovariectomy. NCX1, but not CSQ2, expression was increased postcastration. CSQ2 expression was reduced when H9c2 cells were cultured in hormone-deficient media; increased when estrogen receptor-alpha (ERalpha), estrogen receptor-beta (ERbeta), or androgen agonists were added; and increased in hearts from ERbeta-deficient mice. CSQ2 expression was reduced in mice fed a diet low in the methyl donor folic acid and in cells treated with 5-azadeoxycytidine suggesting an involvement of DNA methylation. DNA methylation in CpG in the CSQ2 CpG island was significantly different in males and females and was additionally changed postgonadectomy. Expression of DNA methyltransferases 1, 3a, and 3b was unchanged. These studies strongly link sex hormone-directed changes in CSQ2 expression to DNA methylation with changed expression correlated with altered left ventricular structure and function. FAU - Sebag, Igal A AU - Sebag IA AD - Division of Cardiology, Sir Mortimer B. Davis-Jewish General Hospital, Montreal, Quebec, Canada. FAU - Gillis, Marc-Antoine AU - Gillis MA FAU - Calderone, Angelino AU - Calderone A FAU - Kasneci, Amanda AU - Kasneci A FAU - Meilleur, Melissa AU - Meilleur M FAU - Haddad, Rami AU - Haddad R FAU - Noiles, William AU - Noiles W FAU - Patel, Bhavini AU - Patel B FAU - Chalifour, Lorraine E AU - Chalifour LE LA - eng GR - Canadian Institutes of Health Research/Canada PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20110729 PL - United States TA - Am J Physiol Heart Circ Physiol JT - American journal of physiology. Heart and circulatory physiology JID - 100901228 RN - 0 (Calsequestrin) RN - 0 (Estrogen Receptor beta) RN - 0 (Gonadal Steroid Hormones) RN - 0 (NCX1 protein, mouse) RN - 0 (Sodium-Calcium Exchanger) RN - 0 (casq2 protein, mouse) RN - SY7Q814VUP (Calcium) SB - IM MH - Animals MH - Base Sequence MH - Calcium/physiology MH - Calsequestrin/genetics/physiology MH - Cell Line MH - DNA Methylation MH - Echocardiography MH - Estrogen Receptor beta/genetics/physiology MH - Female MH - Gene Expression Regulation MH - Gonadal Steroid Hormones/biosynthesis/genetics/*physiology MH - Homeostasis/physiology MH - Male MH - Mice MH - Mice, Inbred C57BL MH - Mice, Knockout MH - Molecular Sequence Data MH - Myocardium/cytology MH - Orchiectomy MH - Ovariectomy MH - Sodium-Calcium Exchanger/genetics MH - Ventricular Function, Left/*physiology EDAT- 2011/08/02 06:00 MHDA- 2011/12/13 00:00 CRDT- 2011/08/02 06:00 PHST- 2011/08/02 06:00 [entrez] PHST- 2011/08/02 06:00 [pubmed] PHST- 2011/12/13 00:00 [medline] AID - ajpheart.00088.2011 [pii] AID - 10.1152/ajpheart.00088.2011 [doi] PST - ppublish SO - Am J Physiol Heart Circ Physiol. 2011 Oct;301(4):H1706-15. doi: 10.1152/ajpheart.00088.2011. Epub 2011 Jul 29.