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Neurological Research
A Journal of Progress in Neurosurgery, Neurology and Neurosciences
Volume 39, 2017 - Issue 11
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Original Research Paper

Sex differences of steroid receptor coactivator-1 expression after spinal cord injury in mice

, , , , , & show all
Pages 1022-1027 | Received 31 Dec 2016, Accepted 09 Aug 2017, Published online: 17 Aug 2017

References

  • Zhang B , Subramanian S , Dziennis S , et al . Estradiol and G1 reduce infarct size and improve immunosuppression after experimental stroke. J Immunol. 2010;184:4087–4094.10.4049/jimmunol.0902339
  • Herson PS , Koerner IP , Hurn PD. Sex, sex steroids, and brain injury. Semin Reprod Med. 2009;27:229–239.10.1055/s-0029-1216276
  • Cui TZ , Hai GF , Zhu ZY , et al . Neuroprotection effects of estrogen on cerebral ischemia in rats. J Xinxiang Med College. 2004;21:246–248.
  • Stem G , Hoffman SW . Estrogen and progesterone as neuroprotective agents in the treatment of acute brain injuries. Pediatr Rehabil. 2003;6:13–22.
  • Correia SC , Santos RX , Cardoso S , et al . Effects of estrogen in the brain: is it a neuroprotective agent in Alzheimers disease? Curr Aging Sci. 2010;3:113–126.10.2174/1874609811003020113
  • Bourque M , Dluzen DE , Di Paolo T . Neuroprotective actions of sex steroids in Parkinson’s disease. Front Neuroendocrinol. 2009;30:142–157.10.1016/j.yfrne.2009.04.014
  • Suzuki S , Brown CM , Wise PM . Neuroprotective effects of estrogens following ischemic stroke. Front Neuroendocrinol. 2009;30:201–211.10.1016/j.yfrne.2009.04.007
  • Sribnick EA , Wingrave JM , Matzelle DD , et al . Estrogen attenuated markers of inflammation and decreased lesion volume in acute spinal cord injury in rats. J Neurosci Res. 2005;82:283–293.10.1002/(ISSN)1097-4547
  • Barker AF , Brautigam VM , Watters JJ . Estrogen modulates microglial inflammatory mediator production via interactions with estrogen receptor β. Endocrinology. 2004;145:5021–5032.10.1210/en.2004-0619
  • Ghisletti S , Meda C , Maggi A , et al . 17 -estradiol inhibits inflammatory gene expression by controlling NF- B intracellular localization. Mol Cell Biol. 2005;25:2957–2968.10.1128/MCB.25.8.2957-2968.2005
  • Lelu K , Delpy L , Robert V , et al . Endogenous estrogens, through estrogen receptor α, constrain autoimmune inflammation in female mice by limiting CD4+ T-cell homing into the CNS. Eur J Immunol. 2010;40:3489–3498.10.1002/eji.201040678
  • Nishihara E , Yoshida-Komiya H , Chan CS , et al . SRC-1 null mice exhibit moderate motor dysfunction and delayed development of cerebellar Purkinje cells. J Neurosci. 2003;23:213–222.
  • Charlier TD , Ball GF , Balthazart J . Plasticity in the expression of the steroid receptor coactivator 1 in the Japanese quail brain: effect of sex, testosterone, stress and time of the day. Neuroscience. 2006;140:1381–1394.10.1016/j.neuroscience.2006.03.002
  • Charlier TD , Cornil CA , Ball GF , et al . Diversity of mechanisms involved in aromatase regulation and estrogen action in the brain. Biochim Biophys Acta. 2010;1800:1094–1105.10.1016/j.bbagen.2009.12.010
  • Tetel MJ . Nuclear receptor coactivators: essential players for steroid hormone action in the brain and in behaviour. J Neuroendocrinol. 2009;21:229–237.10.1111/jne.2009.21.issue-4
  • Xu J , Li Q . Review of the in vivo functions of the p160steroid receptor coactivator family. Mol Endocrinol. 2003;17:1681–1692.
  • Winnay JN , Xu J , O’Malley BW , et al . Steroid receptor coactivator-1-deficient mice exhibit altered hypothalamic-pituitary-adrenal axis function. Endocrinology. 2006;147:1322–1332.10.1210/en.2005-0751
  • Kerver HN , Wade J . Seasonal and sexual dimorphisms in expression of androgen receptor and its coactivators in brain and peripheral copulatory tissues of the green anole. Gen Comp Endocrinol. 2013;193:56–67.10.1016/j.ygcen.2013.07.006
  • Kerver HN , Wade J . Hormonal regulation of steroid receptor coactivator-1 mRNA in the male and female green anole brain. J Neuroendocrinol. 2015;27:223–233.10.1111/jne.2015.27.issue-3
  • Bian C , Zhang D , Guo Q , et al . Localization and sex-difference of steroid receptor coactivator-1 immunoreactivities in the brain of adult female and male mice. Steroids. 2011;76:269–279.10.1016/j.steroids.2010.11.009
  • Plemel JR , Duncan G , Chen KW , et al . A graded forceps crush spinal cord injury model in mice. J Neurotrauma. 2008;25:350–370.10.1089/neu.2007.0426
  • Qiu L , Zhao Y , Guo Q , et al . Dose-dependent regulation of steroid receptor coactivator-1 and steroid receptors by testosterone propionate in the hippocampus of adult male mice. J Steriod Biochem Mol Biol. 2016;156:23–31.10.1016/j.jsbmb.2015.11.012
  • McKenna NJ , O’Malley BW . Combinatorial control of gene expression by nuclear receptors and coregulators. Cell. 2002;108:465–474.10.1016/S0092-8674(02)00641-4
  • Shibata H , Spencer TE , Oñate SA , et al . Role of co-activators and co-repressors in the mechanism of steroid/thyroid receptor action. Recent Prog Horm Res. 1997;52:141–164.
  • Leo C , Chen JD . The SRC family of nuclear receptor coactivators. Gene. 2000;245:1–11.10.1016/S0378-1119(00)00024-X
  • Smith CL , Onate SA , Tsai MJ , et al . CREB binding protein acts synergistically with steroid receptor coactivator-1 to enhance steroid receptor-dependent transcription. Proc Nat Acad Sci. 1996;93:8884–8888.10.1073/pnas.93.17.8884
  • Wu RC , Smith CL , O’Malley BW . Transcriptional regulation by steroid receptor coactivator phosphorylation. Endocr Rev. 2005;26:393–399.10.1210/er.2004-0018
  • Onate SA , Tsai SY , Tsai MJ , et al . Sequence and characterization of a coactivator for the steroid hormone receptor superfamily. Science. 1995;270:1354–1357.
  • Rosenfeld MG , Lunyak VV , Glass CK . Sensors and signals: a coactivator/corepressor/epigenetic code for integrating signal-dependent programs of transcriptional response. Genes Dev. 2006;20:1405–1428.10.1101/gad.1424806
  • Na SY , Lee SK , Han SJ , et al . Steroid receptor coactivator-1 interacts with the p50 subunit and coactivates nuclear factor κB-mediated transactivations. J Biol Chem. 1998;273:10831–10834.10.1074/jbc.273.18.10831
  • Lee SK , Kim HJ , Na SY , et al . Steroid receptor coactivator-1 coactivates activating protein-1-mediated transactivations through interaction with the c-Jun and c-Fos subunits. J Biol Chem. 1998;273:16651–16654.10.1074/jbc.273.27.16651
  • Wu RC , Qin J , Hashimoto Y , et al . Regulation of SRC-3 (pCIP/ACTR/AIB-1/RAC-3/TRAM-1) Coactivator activity by I B kinase. Mol Cell Biol. 2002;22:3549–3561.10.1128/MCB.22.10.3549-3561.2002
  • Kim MS , Sweeney TR , Shigenaga JK , et al . Tumor necrosis factor and interleukin 1 decrease RXRα, PPARα, PPARγ, LXRα, and the coactivators SRC-1, PGC-1α, and PGC-1β in liver cells. Metabolism. 2007;56:267–279.10.1016/j.metabol.2006.10.007
  • Du ZY , Su YP , Yang TD , et al . Effect of SRC-1 deficiency on the expression and nuclear translocation of NF-κB in mice after burn injury. Chongqing Med. 2008;37:1897–1899. Chinese.
  • Sahar S , Reddy MA , Wong C , et al . Cooperation of SRC-1 and p300 With NF- B and CREB in angiotensin II-induced IL-6 expression in vascular smooth muscle cells. Arterioscler Thromb Vasc Biol. 2007;27:1528–1534.10.1161/ATVBAHA.107.145862
  • Guo Q , Cheng J , Zhang J , et al . Delayed post-injury administration o C5a improves regeneration and functional recovery after spinal cord injury in mice. Clin Exp Immunol. 2013;174:318–325.
  • Vidal PM , Lemmens E , Geboes L , et al . Late blocking of peripheral TNF-α is ineffective after spinal cord injury in mice. Immunobiology. 2013;218:281–284.10.1016/j.imbio.2012.05.007
  • Brennan FH , Anderson AJ , Taylor SM , et al . Complement activation in the injured central nervous system: another dual-edged sword? J Neuroinflammation. 2012;9:137–149.
  • Beck KD , Nguyen HX , Galvan MD , et al . Quantitative analysis of cellular inflammation after traumatic spinal cord injury: evidence for a multiphasic inflammatory response in the acute to chronic environment. Brain. 2010;133:433–447.10.1093/brain/awp322
  • Zhang D , Guo Q , Bian C , et al . Alterations of steroid receptor coactivator-1 (SRC-1) immunoreactivities in specific brain regions of young and middle-aged female Sprague–Dawley rats. Brain Res. 2011;1382:88–97.10.1016/j.brainres.2011.01.024
  • Grenier J , Trousson A , Chauchereau A , et al . Selective recruitment of p160 coactivators on glucocorticoid-regulated promoters in Schwann cells. Mol Endocrinol. 2004;18:2866–2879.10.1210/me.2004-0241
  • Hojo Y , Murakami G , Mukai H , et al . Estrogen synthesis in the brain-role in synaptic plasticity and memory. Mol Cell Endocrinol. 2008;290:31–43.10.1016/j.mce.2008.04.017
  • Zhang JQ , Cai WQ . Research progress of brain estrogen receptor. J Regional Anat Operative Surg. 2009;18:1–2. Chinese.
  • Witke W . The role of profilin complexes in cell motility and other cellular processes. Trends Cell Biol. 2004;14:461–469.10.1016/j.tcb.2004.07.003
  • Horrevoets AJ . Profilin-1: an unexpected molecule linking vascular inflammation to the actin cytoskeleton. Circ Res. 2007;101:328–330.10.1161/CIRCRESAHA.107.158881
  • Zhao Y , Yu Y , Zhang Y , et al . Letrozole regulates actin cytoskeleton polymerization dynamics in a SRC-1 dependent manner in the hippocampus of mice. J Steroid Biochem Mol Biol. 2016;17: Epub ahead of print.

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