Effects of trichostatin A, a histone deacetylase inhibitor, on mouse gonadal development in vitro
Sry, Sox9 and M33 are thought to act as architectural transcription factors or as a chromatin regulator in gonadal development. However, the direct relationship between chromatin structure and sex determination has not yet been revealed. To clarify the effect of chromatin structural change on gonada...
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Published in | Journal of Reproduction and Development Vol. 50; no. 2; pp. 227 - 235 |
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01.04.2004
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Abstract | Sry, Sox9 and M33 are thought to act as architectural transcription factors or as a chromatin regulator in gonadal development. However, the direct relationship between chromatin structure and sex determination has not yet been revealed. To clarify the effect of chromatin structural change on gonadal development, we examined the effects of trichostatin A, a histone deacetylase inhibitor, on mouse gonadal development in vitro. In the 0.1 microM treated testicular explants, the size of the gonad was significantly decreased, although the testicular cord formation occurred normally. In the 1.0 microM treated explants, the gonads revealed one or two large testicular cords. Sox9 and MIS expressions suggest that Sertoli cell differentiation is induced normally within the testicular cord, while Dnmt3b expression suggests that several immature Sertoli cells are located on the outside of the testicular cord. The 3v-hsd expression indicates that Leydig cell differentiation occurs normally. On the other hand, germ cell loss was observed in the treated testicular explants. In the treated ovarian explants, the number of premeiotic germ cells was reduced without gonadal size change. Thus, trichostatin A affects the development of germ cells, but does not affect sex determination. |
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AbstractList | Sry, Sox9 and M33 are thought to act as architectural transcription factors or as a chromatin regulator in gonadal development. However, the direct relationship between chromatin structure and sex determination has not yet been revealed. To clarify the effect of chromatin structural change on gonadal development, we examined the effects of trichostatin A, a histone deacetylase inhibitor, on mouse gonadal development in vitro. In the 0.1 μM treated testicular explants, the size of the gonad was significantly decreased, although the testicular cord formation occurred normally. In the 1.0 μM treated explants, the gonads revealed one or two large testicular cords. Sox9 and MIS expressions suggest that Sertoli cell differentiation is induced normally within the testicular cord, while Dnmt3b expression suggests that several immature Sertoli cells are located on the outside of the testicular cord. The 3β-hsd expression indicates that Leydig cell differentiation occurs normally. On the other hand, germ cell loss was observed in the treated testicular explants. In the treated ovarian explants, the number of premeiotic germ cells was reduced without gonadal size change. Thus, trichostatin A affects the development of germ cells, but does not affect sex determination. Sry, Sox9 and M33 are thought to act as architectural transcription factors or as a chromatin regulator in gonadal development. However, the direct relationship between chromatin structure and sex determination has not yet been revealed. To clarify the effect of chromatin structural change on gonadal development, we examined the effects of trichostatin A, a histone deacetylase inhibitor, on mouse gonadal development in vitro. In the 0.1 mu M treated testicular explants, the size of the gonad was significantly decreased, although the testicular cord formation occurred normally. In the 1.0 mu M treated explants, the gonads revealed one or two large testicular cords. Sox9 and MIS expressions suggest that Sertoli cell differentiation is induced normally within the testicular cord, while Dnmt3b expression suggests that several immature Sertoli cells are located on the outside of the testicular cord. The 3 beta -hsd expression indicates that Leydig cell differentiation occurs normally. On the other hand, germ cell loss was observed in the treated testicular explants. In the treated ovarian explants, the number of premeiotic germ cells was reduced without gonadal size change. Thus, trichostatin A affects the development of germ cells, but does not affect sex determination. Sry, Sox9 and M33 are thought to act as architectural transcription factors or as a chromatin regulator in gonadal development. However, the direct relationship between chromatin structure and sex determination has not yet been revealed. To clarify the effect of chromatin structural change on gonadal development, we examined the effects of trichostatin A, a histone deacetylase inhibitor, on mouse gonadal development in vitro. In the 0.1 microM treated testicular explants, the size of the gonad was significantly decreased, although the testicular cord formation occurred normally. In the 1.0 microM treated explants, the gonads revealed one or two large testicular cords. Sox9 and MIS expressions suggest that Sertoli cell differentiation is induced normally within the testicular cord, while Dnmt3b expression suggests that several immature Sertoli cells are located on the outside of the testicular cord. The 3beta-hsd expression indicates that Leydig cell differentiation occurs normally. On the other hand, germ cell loss was observed in the treated testicular explants. In the treated ovarian explants, the number of premeiotic germ cells was reduced without gonadal size change. Thus, trichostatin A affects the development of germ cells, but does not affect sex determination. Sry, Sox9 and M33 are thought to act as architectural transcription factors or as a chromatin regulator in gonadal development. However, the direct relationship between chromatin structure and sex determination has not yet been revealed. To clarify the effect of chromatin structural change on gonadal development, we examined the effects of trichostatin A, a histone deacetylase inhibitor, on mouse gonadal development in vitro. In the 0.1 microM treated testicular explants, the size of the gonad was significantly decreased, although the testicular cord formation occurred normally. In the 1.0 microM treated explants, the gonads revealed one or two large testicular cords. Sox9 and MIS expressions suggest that Sertoli cell differentiation is induced normally within the testicular cord, while Dnmt3b expression suggests that several immature Sertoli cells are located on the outside of the testicular cord. The 3v-hsd expression indicates that Leydig cell differentiation occurs normally. On the other hand, germ cell loss was observed in the treated testicular explants. In the treated ovarian explants, the number of premeiotic germ cells was reduced without gonadal size change. Thus, trichostatin A affects the development of germ cells, but does not affect sex determination. |
Author | Fujisawa, M Kurohmaru, M Kanai, Y Hayashi, Y Mizukami, T. (Tokyo Univ. (Japan)) |
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References_xml | – volume: 228 start-page: 173 issn: 0022-104X year: 1983 ident: 28 publication-title: J Exp Zool doi: 10.1002/jez.1402280204 contributor: fullname: Zamboni L, Upadhyay S – volume: 113 start-page: 613 issn: 0950-1991 year: 1991 ident: 19 publication-title: Development doi: 10.1242/dev.113.2.613 contributor: fullname: Munsterberg A, Lovell-Badge R – ident: 25 doi: 10.1128/MCB.23.17.6000-6012.2003 – ident: 27 doi: 10.1242/dev.00836 – ident: 11 doi: 10.1126/science.1063127 – ident: 16 doi: 10.1292/jvms.63.31 – volume: 109 start-page: 899 issn: 0021-9533 issue: 5 year: 1996 ident: 20 publication-title: J Cell Sci doi: 10.1242/jcs.109.5.899 – volume: 122 start-page: 2813 issn: 0950-1991 issue: 9 year: 1996 ident: 18 publication-title: Development doi: 10.1242/dev.122.9.2813 – ident: 8 doi: 10.1074/jbc.274.35.25113 – ident: 4 doi: 10.1016/S0959-437X(97)80147-5 – ident: 32 doi: 10.1002/mc.10145 – volume: 255 start-page: 453 issn: 0036-8075 issue: 5043 year: 1992 ident: 3 publication-title: Science doi: 10.1126/science.1734522 – ident: 13 doi: 10.1139/bcb-79-3-305 – volume: 57 start-page: 1 issn: 0079-9963 year: 2002 ident: 1 publication-title: Recent Prog Horm Res doi: 10.1210/rp.57.1.1 contributor: fullname: Tilmann C, Capel B – volume: 112 start-page: 2441 issn: 0021-9533 issue: 14 year: 1999 ident: 30 publication-title: J Cell Sci doi: 10.1242/jcs.112.14.2441 contributor: fullname: RYAN J – volume: 91 start-page: 1216 issn: 0006-4971 year: 1998 ident: 17 publication-title: Blood doi: 10.1182/blood.V91.4.1216 contributor: fullname: Lessard J, Baban S, Sauvageau G – volume: 14 start-page: 119 issn: 0192-253X issue: 2 year: 1993 ident: 22 publication-title: Dev Genet doi: 10.1002/dvg.1020140206 – ident: 5 doi: 10.1038/31482 – volume: 86 start-page: 41 issn: 0065-230X year: 2002 ident: 10 publication-title: Adv Cancer Res doi: 10.1016/S0065-230X(02)86002-X contributor: fullname: Lehrmann H, Pritchard LL, Harel-Bellan A – ident: 24 doi: 10.1016/S0012-1606(03)00122-2 – volume: 265 start-page: 17174 issn: 0021-9258 issue: 28 year: 1990 ident: 12 publication-title: J Biol Chem doi: 10.1016/S0021-9258(17)44885-X – ident: 2 doi: 10.1038/346240a0 – volume: 125 start-page: 889 issn: 0950-1991 issue: 5 year: 1998 ident: 21 publication-title: Development doi: 10.1242/dev.125.5.889 – volume: 230 start-page: 199 issn: 0003-276X year: 1991 ident: 15 publication-title: Anat Rec doi: 10.1002/ar.1092300207 contributor: fullname: Kanai Y, Hayashi Y, Kawakami H, Takata K, Kurohmaru M, Hirano H, Nishida T – volume: 5 start-page: 269 issn: 1087-2957 year: 2003 ident: 33 publication-title: Prog Cell Cycle Res contributor: fullname: Yoshida M, Shimazu T, Matsuyama A – ident: 14 doi: 10.1038/11981 – volume: 322 start-page: 3 issn: 0962-8436 year: 1988 ident: 26 publication-title: Philos Trans R Soc Lond B Biol Sci doi: 10.1098/rstb.1988.0109 contributor: fullname: McLaren A – volume: 9 start-page: 217 issn: 1072-8368 year: 2002 ident: 23 publication-title: Nat Struct Biol contributor: fullname: Qiu C, Sawada K, Zhang X, Cheng X – ident: 31 doi: 10.1083/jcb.200303047 – volume: 167 start-page: 866 issn: 0022-1767 issue: 2 year: 2001 ident: 6 publication-title: J Immunol doi: 10.4049/jimmunol.167.2.866 contributor: fullname: MAEES J – ident: 7 doi: 10.1038/ni0703-616 – ident: 29 doi: 10.1016/S0925-4773(02)00242-3 – ident: 9 doi: 10.1016/S0168-9525(03)00115-X |
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SubjectTerms | Animals Anti-Mullerian Hormone Apoptosis Cell Differentiation - drug effects Cell Division - drug effects CHROMATIN Chromatin - metabolism DNA (Cytosine-5-)-Methyltransferases - biosynthesis Dose-Response Relationship, Drug ENZYME INHIBITORS Enzyme Inhibitors - pharmacology Female GAMETES GENITALIA Germ cell Germ Cells - drug effects Glycoproteins - metabolism Gonad Gonads - cytology Gonads - metabolism Histone acetylation Histone Deacetylase Inhibitors Hydroxamic Acids - pharmacology IN VITRO EXPERIMENTATION Male MICE Mice, Inbred ICR Organ Culture Techniques Reverse Transcriptase Polymerase Chain Reaction RNA - metabolism Sertoli Cells - cytology Sertoli Cells - ultrastructure Sex determination SEX DIFFERENTIATION Sex Factors Testicular Hormones - metabolism Testis - drug effects Testis - metabolism Testis - ultrastructure Time Factors Transcription, Genetic Trichostatin A |
Title | Effects of trichostatin A, a histone deacetylase inhibitor, on mouse gonadal development in vitro |
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