Kwon Dae Jin, Lee Yu Mi, Hwang In Sun, Park Choon Keun, Yang Boo Keun, Cheong Hee Tae
College of Veterinary Medicine and Institute of Veterinary Science, Kangwon National University, Chuncheon 200-701, Korea.
J Vet Sci. 2010 Jun;11(2):93-101. doi: 10.4142/jvs.2010.11.2.93.
This study was conducted to evaluate the microtubule distribution following control of nuclear remodeling by treatment of bovine somatic cell nuclear transfer (SCNT) embryos with caffeine or roscovitine. Bovine somatic cells were fused to enucleated oocytes treated with either 5 mM caffeine or 150 microM roscovitine to control the type of nuclear remodeling. The proportion of embryos that underwent premature chromosome condensation (PCC) was increased by caffeine treatment but was reduced by roscovitine treatment (p < 0.05). The microtubule organization was examined by immunostaining beta- and gamma-tubulins at 15 min, 3 h, and 20 h of fusion using laser scanning confocal microscopy. The gamma-tubulin foci inherited from the donor centrosome were observed in most of the SCNT embryos at 15 min of fusion (91.3%) and most of them did not disappear until 3 h after fusion, regardless of treatment (82.9-87.2%). A significantly high proportion of embryos showing an abnormal chromosome or microtubule distribution was observed in the roscovitinetreated group (40.0%, p < 0.05) compared to the caffeinetreated group (22.1%). In conclusion, PCC is a favorable condition for the normal organization of microtubules, and inhibition of PCC can cause abnormal mitotic division of bovine SCNT embryos by causing microtubule dysfunction.
本研究旨在通过用咖啡因或罗哌卡因处理牛体细胞核移植(SCNT)胚胎来控制核重塑后,评估微管分布。将牛体细胞与用5 mM咖啡因或150 microM罗哌卡因处理的去核卵母细胞融合,以控制核重塑的类型。咖啡因处理增加了经历早熟染色体凝聚(PCC)的胚胎比例,但罗哌卡因处理降低了该比例(p < 0.05)。在融合后15分钟、3小时和20小时,使用激光扫描共聚焦显微镜通过免疫染色β-和γ-微管蛋白来检查微管组织。在融合后15分钟,大多数SCNT胚胎(91.3%)中观察到从供体中心体遗传的γ-微管蛋白焦点,并且无论处理如何,大多数焦点在融合后3小时之前都不会消失(82.9 - 87.2%)。与咖啡因处理组(22.1%)相比,罗哌卡因处理组中观察到异常染色体或微管分布的胚胎比例显著更高(40.0%,p < 0.05)。总之,PCC是微管正常组织的有利条件,抑制PCC可通过导致微管功能障碍引起牛SCNT胚胎的异常有丝分裂。