Department of Medical Research and Education, National Yang-Ming University Hospital, Yilan, Taiwan, Republic of China.
J Biomed Sci. 2012 Jul 9;19(1):63. doi: 10.1186/1423-0127-19-63.
Dysmorphogenesis and multiple organ defects are well known in zebrafish (Danio rerio) embryos with T-box transcription factor 5 (tbx5) deficiencies, mimicking human Holt-Oram syndrome.
Using an oligonucleotide-based microarray analysis to study the expression of special genes in tbx5 morphants, we demonstrated that GH and some GH-related genes were markedly downregulated. Zebrafish embryos microinjected with tbx5-morpholino (MO) antisense RNA and mismatched antisense RNA in the 1-cell stage served as controls, while zebrafish embryos co-injected with exogenous growth hormone (GH) concomitant with tbx5-MO comprised the treatment group.
The attenuating effects of GH in tbx5-MO knockdown embryos were quantified and observed at 24, 30, 48, 72, and 96 h post-fertilization. Though the understanding of mechanisms involving GH in the tbx5 functioning complex is limited, exogenous GH supplied to tbx5 knockdown zebrafish embryos is able to enhance the expression of downstream mediators in the GH and insulin-like growth factor (IGF)-1 pathway, including igf1, ghra, and ghrb, and signal transductors (erk1, akt2), and eventually to correct dysmorphogenesis in various organs including the heart and pectoral fins. Supplementary GH also reduced apoptosis as determined by a TUNEL assay and decreased the expression of apoptosis-related genes and proteins (bcl2 and bad) according to semiquantitative reverse-transcription polymerase chain reaction and immunohistochemical analysis, respectively, as well as improving cell cycle-related genes (p27 and cdk2) and cardiomyogenetic genes (amhc, vmhc, and cmlc2).
Based on our results, tbx5 knockdown causes a pseudo GH deficiency in zebrafish during early embryonic stages, and supplementation of exogenous GH can partially restore dysmorphogenesis, apoptosis, cell growth inhibition, and abnormal cardiomyogenesis in tbx5 knockdown zebrafish in a paracrine manner.
T 盒转录因子 5(tbx5)缺陷的斑马鱼胚胎中存在畸形发生和多个器官缺陷,类似于人类 Holt-Oram 综合征。
我们使用基于寡核苷酸的微阵列分析来研究 tbx5 形态发生缺陷体中特殊基因的表达,结果表明 GH 和一些 GH 相关基因显著下调。在 1 细胞期用 tbx5 反义 RNA 的寡核苷酸(MO)显微注射的斑马鱼胚胎和用错配的反义 RNA 显微注射的斑马鱼胚胎作为对照,而用外源性生长激素(GH)与 tbx5-MO 共同显微注射的斑马鱼胚胎作为处理组。
在受精后 24、30、48、72 和 96 小时,对 GH 在 tbx5-MO 敲低胚胎中的抑制作用进行了量化和观察。尽管对 GH 参与 tbx5 功能复合物的机制的了解有限,但外源性 GH 供给 tbx5 敲低斑马鱼胚胎能够增强 GH 和胰岛素样生长因子(IGF)-1 途径中的下游介质的表达,包括 igf1、ghra 和 ghrb 以及信号转导物(erk1、akt2),最终纠正包括心脏和胸鳍在内的各种器官的畸形发生。补充 GH 还通过 TUNEL 测定减少了凋亡,并根据半定量逆转录聚合酶链反应和免疫组织化学分析分别降低了凋亡相关基因和蛋白(bcl2 和 bad)的表达,以及改善了细胞周期相关基因(p27 和 cdk2)和心肌发生基因(amhc、vmhc 和 cmlc2)的表达。
根据我们的结果,tbx5 敲低导致早期胚胎阶段的斑马鱼假性 GH 缺乏,外源性 GH 的补充可以以旁分泌的方式部分恢复 tbx5 敲低斑马鱼的畸形发生、凋亡、细胞生长抑制和异常心肌发生。