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咖啡因、冈田酸和染料木黄酮对经X射线照射而停滞于G2期的单细胞小鼠胚胎的形态学影响。

Morphological effects of caffeine, okadaic acid and genistein in one-cell mouse embryos blocked in G2 by X-irradiation.

作者信息

Jacquet P, de Saint-Georges L, Barrio S, Baugnet-Mahieu L

机构信息

Laboratory of Radiobiology, Department of Radioprotection, Mol, Belgium.

出版信息

Int J Radiat Biol. 1995 Mar;67(3):347-58. doi: 10.1080/09553009514550401.

Abstract

One-cell mouse embryos of the Balb/c strain normally divide at 18.5 h p.c. (post conception), but they suffer an extremely long G2 arrest when irradiated with 2 Gy X-rays 8 h p.c. at the early pronuclear stage. This could be an indirect effect of radiation on tyrosine dephosphorylation of the p34cdc2 subunit of a maturation or mitosis promoting factor (MPF), which normally occurs at the end of G2. This, in turn, would maintain MPF in an inactivated form and block entry into mitosis. Preliminary studies were undertaken at the morphological level to assess indirectly the validity of this hypothesis. For this purpose, irradiated and control embryos were exposed to different compounds, which are known to interfere, directly or indirectly, with the state of phosphorylation/dephosphorylation of p34cdc2. Caffeine (CAF; 2 mM) did not affect the time of first division of control embryos, but it completely suppressed the radiation-induced G2 arrest of embryos exposed to this compound from 17 h p.c., i.e. 1.5 h before the normal time of first cleavage. Under the same conditions, okadaic acid (OA; 3 microM), a specific inhibitor of phosphatases I and IIA, induced a rapid pronuclear membrane breakdown and a block of all control and irradiated embryos at metaphase. Genistein (GEN; 92 or 185 microM). A potent inhibitor of tyrosine kinases, increased the radiation-induced G2 arrest and even induced a dose-dependent G2 arrest in the control embryos. Embryos were exposed at different times following irradiation to a mixture of either CAF (2 or 5 mM) or OA (3 or 10 microM), and cycloheximide (CH; 5 micrograms/ml), a potent protein synthesis inhibitor. Reversion of G2-arrest by CAF was still seen in embryos exposed to CAF+CH from 17 h p.c. However, the proportion of irradiated embryos eventually able to cleave was lower than that obtained under the conditions of exposure to CAF alone. Embryos exposed to CAF+CH before 17 h p.c. were not able to cleave, regardless of the concentration of CAF used. Nuclear envelope breakdown still occurred in 100% control and irradiated embryos, following exposure to 3 microM OA+CH from 10 h p.c., or to 10 microM OA+CH from 8.5 p.c.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

Balb/c品系的单细胞小鼠胚胎通常在受孕后18.5小时分裂,但在原核早期受孕后8小时用2 Gy X射线照射时,它们会经历极长的G2期阻滞。这可能是辐射对成熟或有丝分裂促进因子(MPF)的p34cdc2亚基酪氨酸去磷酸化的间接影响,这种去磷酸化通常发生在G2期末。反过来,这会使MPF维持在失活状态并阻止进入有丝分裂。在形态学水平上进行了初步研究,以间接评估该假设的有效性。为此,将受照射和对照胚胎暴露于不同的化合物中,已知这些化合物会直接或间接干扰p34cdc2的磷酸化/去磷酸化状态。咖啡因(CAF;2 mM)不影响对照胚胎的首次分裂时间,但它完全抑制了从受孕后17小时(即正常首次分裂时间前1.5小时)暴露于该化合物的胚胎的辐射诱导的G2期阻滞。在相同条件下,冈田酸(OA;3 microM),一种磷酸酶I和IIA的特异性抑制剂,诱导原核膜快速破裂,并使所有对照和受照射胚胎在中期阻滞。染料木黄酮(GEN;92或185 microM),一种酪氨酸激酶的有效抑制剂,增加了辐射诱导并使对照胚胎出现剂量依赖性的G2期阻滞。在照射后的不同时间,将胚胎暴露于CAF(2或5 mM)或OA(3或10 microM)与环己酰亚胺(CH;5微克/毫升)的混合物中,环己酰亚胺是一种有效的蛋白质合成抑制剂。从受孕后17小时开始暴露于CAF+CH的胚胎中,仍可观察到CAF对G2期阻滞的逆转。然而,最终能够分裂的受照射胚胎的比例低于仅暴露于CAF的条件下获得的比例。无论使用的CAF浓度如何,在受孕后17小时之前暴露于CAF+CH的胚胎都无法分裂。从受孕后10小时开始暴露于3 microM OA+CH,或从受孕后8.5小时开始暴露于10 microM OA+CH后,100%的对照和受照射胚胎仍会发生核膜破裂。(摘要截断于400字)

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