[164] A. Cevasco, R. Urbatzka, S. Bottero, A.Massari, F. Pedemonte,W. Kloas, A.Mandich, Endocrine disrupting chemicals (EDC) with (anti)estrogenic and (anti)androgenic modes of action affecting reprod
[164] A. Cevasco, R. Urbatzka, S. Bottero, A.Massari, F. Pedemonte,W. Kloas, A.Mandich, Endocrine disrupting chemicals (EDC) with (anti)estrogenic and (anti)androgenic modes of action affecting reproductive biology of Xenopus laevis: II. Effects on gonad histomorphology, Comp. Biochem. Physiol. Toxicol. Pharmacol. 147 (2008) 241–251.
[165] A.R. Tompsett, S. Wiseman, E. Higley, J.P. Giesy, M. Hecker, Effects of exposure to 17alpha-ethynylestradiol during larval development on growth, sexual differentiation, and abundances of transcripts in the liver of the wood frog (Lithobates sylvaticus), Aquat. Toxicol. 126 (2013) 42–51.
[166] P. Duarte-Guterman, L. Navarro-Martin, V.L. Trudeau, Mechanisms of crosstalk between endocrine systems: regulation of sex steroid hormone synthesis and action by thyroid hormones, Gen. Comp. Endocrinol. (2014), in press [Epub ahead of print].
[167] V. Martinez-Cerdeno, S.C. Noctor, A.R. Kriegstein, Estradiol stimulates progenitor cell pision in the ventricular and subventricular zones of the embryonic neocortex, Eur. J. Neurosci. 24 (2006) 3475–3488.
[168] S. Ijiri, C. Berard, J.M. Trant, Characterization of gonadal and extra-gonadal forms of the cDNA encoding the Atlantic stingray (Dasyatis sabina) cytochrome P450 aromatase (CYP19), Mol. Cell. Endocrinol. 164 (2000) 169–181.
[169] S. Ijiri, Y. Kazeto, P.M. Lokman, S. Adachi, K. Yamauchi, Characterization of a cDNA encoding P-450 aromatase (CYP19) from Japanese eel ovary and its expression in ovarian follicles during induced ovarian development, Gen. Comp. Endocrinol. 130 (2003) 193–203.
[170] S.R. Jeng, S. Dufour, C.F. Chang, Differential expression of neural and gonadal aromatase enzymatic activities in relation to gonadal development in Japanese eel, Anguilla japonica, J. Exp. Zool. A Comp. Exp. Biol. 303 (2005) 802–812.
[171] S.R. Jeng, J. Pasquier, W.S. Yueh, G.R. Chen, Y.H. Lee, S. Dufour, C.F. Chang, Differential regulation of the expression of cytochrome P450 aromatase, estrogen and androgen receptor subtypes in the brain–pituitary–ovarian axis of the Japanese eel (Anguilla japonica) reveals steroid dependent and independent mechanisms, Gen. Comp. Endocrinol. 175 (2012) 163–172.
[172] C.V. Henkel, E. Burgerhout, D.L. de Wijze, R.P. Dirks, Y. Minegishi, H.J. Jansen, H.P. Spaink, S. Dufour, F.A. Weltzien, K. Tsukamoto, G.E. van den Thillart, Primitive duplicate Hox clusters in the European eel's genome, PLoS One 7 (2012) e32231.
[173] K.M. Choi, J.Y. Kim, Y. Kim, Distribution of the immunoreactivity for glycoprotein M6B in the neurogenic niche and reactive glia in the injury penumbra following traumatic brain injury in mice, Exp. Neurobiol. 22 (2013) 277–282.
[174] Y. Goldshmit, F. Frisca, A.R. Pinto, A. Pebay, J.K. Tang, A.L. Siegel, J. Kaslin, P.D. Currie, Fgf2 improves functional recovery-decreasing gliosis and increasing radial glia and neural progenitor cells after spinal cord injury, Brain Behav. 4 (2014) 187–200.
[175] Y. Guo, Q. Wei, Y. Huang, W. Xia, Y. Zhou, S. Wang, The effects of astrocytes on differentiation of neural stemcells are influenced by knock-down of the glutamate transporter, GLT-1, Neurochem. Int. 63 (2013) 498–506.
[176] B. Saha, S. Peron, K. Murray, M. Jaber, A. Gaillard, Cortical lesion stimulates adultsubventricular zone neural progenitor cell proliferation and migration to the site of injury, Stem Cell Res. 11 (2013) 965–977.
[177] M.R. Costa, M. Gotz, B. Berninger, What determines neurogenic competence in glia? Brain Res. Rev. 63 (2010) 47–59.
附外文文献原文
Abstract
Estrogens affect brain development of vertebrates, not only by impacting activity and morphology of existing circuits, but also by modulating embryonic and adult neurogenesis. The issue is complex as estrogens can not only originate from peripheral tissues, but also be locally produced within the brain itself due to local aromatiza-tion of androgens. In this respect, teleost fishes are quite unique because aromatase is expressed exclusively in radial glial cells, which represent pluripotent cells in the brain of all vertebrates. Expression of aromatase in the brain of fish is also strongly stimulated by estrogens and some androgens. This creates a very intriguing positive auto-regulatory loop leading to dramatic aromatase expression in sexually mature fish with elevated levels of circulating steroids. Looking at the effects of estrogens or anti-estrogens in the brain of adult zebrafish showed that estrogens inhibit rather than stimulate cell proliferation and newborn cell migration. The functional meaning of these observations is still unclear, but these data suggest that the brain of fish is experiencing constant remodeling under the influence of circulating steroids and brain-derived neurosteroids, possibly permitting a persification of sexual strategies, notably hermaphroditism. Recent data in frogs indicate that aromatase expression is limited to neurons and do not concern radial glial cells. Thus, until now, there is no other example of vertebrates in which radial progenitors express aromatase. This raises the question of when and why these new features were gained and what are their adaptive benefits. This article is part of a Special Issue entitled: Nuclear receptors in animal development.