Tian W X, Zhang W P, Li J K, Bi D R, Guo D Z, Pan S Y, Zhang Y H, Qin P
State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.
Avian Pathol. 2009 Apr;38(2):161-6. doi: 10.1080/03079450902737789.
Tibial dyschondroplasia (TD) is characterized by expansion of the proximal growth plates of the tibiotarsus that fail to form bone, lack blood vessels, and contain non-viable cells. Thiram (a carbamate pesticide), when fed to young broiler chicks, induces TD with high regularity and precision. We used this experimental model to understand the cause of the defects associated with TD by selecting and identifying the genes differentially expressed in the TD growth plate of broiler chickens. Broiler chicks at 7 days of age were randomly divided into two groups. After fasting overnight, they were fed with regular diet (control) or the same diet containing 100 mg/kg thiram for 96 h to induce TD (thiram-fed). mRNA was purified from the growth plates of control and thiram-fed broilers. Forward and reverse-subtracted cDNA libraries were generated by suppression subtractive hybridization technology. Ten selected genes from cDNA libraries were identified by real-time quantitative polymerase chain reaction. All were differentially expressed in TD growth plates (P<0.05 or P<0.01). The levels of collagen type X (Col X), pro-alpha-1 collagen type I (Col I alpha1), collagen type IX (Col IX), NADH dehydrogenase (NADH DH), cytochrome C oxidase subunit III (COX III), enolase 1, alpha (ENO1), carbonic anhydrase II (CA2) and heat shock protein 90 (Hsp90) mRNA transcripts were up-regulated, while the expression levels of Matrilin 3 (MATN3) and chondromodulin-I (ChM-I) were down-regulated. Col I and Hsp90 were detected by immunohistochemistry at different stages. Given that these genes are involved in matrix formation, endochondral ossification, developmental regulation, electron transport in the mitochondrial respiratory chain and vascularization, our findings may provide new insights into understanding the pathogenesis of TD.
胫骨软骨发育不良(TD)的特征是胫跗骨近端生长板扩张,该生长板无法形成骨骼,缺乏血管且含有无活力的细胞。福美双(一种氨基甲酸酯类农药)喂给幼龄肉鸡时,会以高规律性和精确性诱发TD。我们利用这个实验模型,通过选择和鉴定在肉鸡TD生长板中差异表达的基因,来了解与TD相关的缺陷的原因。7日龄的肉鸡随机分为两组。禁食过夜后,一组喂常规饲料(对照组),另一组喂含100 mg/kg福美双的相同饲料96小时以诱发TD(福美双喂养组)。从对照组和福美双喂养组肉鸡的生长板中纯化mRNA。通过抑制性消减杂交技术构建正向和反向消减cDNA文库。通过实时定量聚合酶链反应鉴定cDNA文库中选出的10个基因。所有这些基因在TD生长板中均差异表达(P<0.05或P<0.01)。X型胶原(Col X)、I型前α1胶原(Col I alpha1)、IX型胶原(Col IX)、NADH脱氢酶(NADH DH)、细胞色素C氧化酶亚基III(COX III)、烯醇化酶1α(ENO1)、碳酸酐酶II(CA2)和热休克蛋白90(Hsp90)的mRNA转录水平上调,而基质金属蛋白酶3(MATN3)和软骨调节素-I(ChM-I)的表达水平下调。在不同阶段通过免疫组织化学检测Col I和Hsp90。鉴于这些基因参与基质形成、软骨内骨化、发育调控、线粒体呼吸链中的电子传递和血管生成,我们的研究结果可能为理解TD的发病机制提供新的见解。