Torres Vicente E, Sweeney William E, Wang Xiaofang, Qian Qi, Harris Peter C, Frost Philip, Avner Ellis D
Mayo Foundation, Rochester, Minnesota, USA.
Kidney Int. 2004 Nov;66(5):1766-73. doi: 10.1111/j.1523-1755.2004.00952.x.
Advances in the understanding of cystogenesis, identification of the PKHD1 gene and availability of a rat model (the PCK rat) caused by a Pkhd1 mutation facilitate testing of therapies for autosomal-recessive polycystic kidney disease (ARPKD). Considerable support exists for the importance of the epidermal growth factor (EGF)/transforming growth factor-alpha (TGF-alpha)/EGF receptor (EGFR) axis and of the adenylyl cyclase-adenosine 3',5'-cyclic monophosphate (cAMP) pathway in the pathogenesis of cyst formation and progressive enlargement.
To determine whether EGFR tyrosine kinase inhibition is protective in the PCK rat, male and female animals were treated with EKI-785 or EKB-569 or with vehicle alone between 3 and 10 weeks of age. Biochemical and histomorphometric analysis, immunohistochemistry, immunoblotting, enzyme immunoassay, and quantitative reverse transcription-polymerase chain reaction (RT-PCR) were used to ascertain the effects of treatment.
Contrary to other murine models of ARPKD, overexpression and apical mislocalization of EGFR were not detected in the PCK rats. Consistent with these expression results, EKI-785 or EKB-569 administration had no effect or worsened PKD, and had no effect on the development of fibrocystic liver disease. Increased renal cAMP and vasopressin V2 receptor expression were observed in the EKI-785-treated animals.
EGFR tyrosine kinase inhibition did not protect PCK rats from the development of PKD. This may be due to effects on collecting duct cAMP that counteract possible beneficial effects on the extracellular-regulated protein kinase (ERK)/mitogen-activated protein kinase (MAPK) pathway, particularly in the absence of EGFR overexpression or mislocalization. The relevance of these observations to the treatment of human cystic kidney diseases deserves further study.
对囊肿发生机制的认识进展、PKHD1基因的鉴定以及由Pkhd1突变引起的大鼠模型(PCK大鼠)的出现,有助于对常染色体隐性多囊肾病(ARPKD)的治疗方法进行测试。表皮生长因子(EGF)/转化生长因子-α(TGF-α)/EGF受体(EGFR)轴以及腺苷酸环化酶-3',5'-环磷酸腺苷(cAMP)途径在囊肿形成和逐渐增大的发病机制中的重要性得到了相当多的支持。
为了确定EGFR酪氨酸激酶抑制在PCK大鼠中是否具有保护作用,在3至10周龄之间,对雄性和雌性动物用EKI-785或EKB-569或仅用赋形剂进行治疗。使用生化和组织形态计量分析、免疫组织化学、免疫印迹、酶免疫测定以及定量逆转录-聚合酶链反应(RT-PCR)来确定治疗效果。
与其他ARPKD小鼠模型相反,在PCK大鼠中未检测到EGFR的过表达和顶端错位。与这些表达结果一致,给予EKI-785或EKB-569对PKD没有影响或使其恶化,并且对纤维囊性肝病的发展没有影响。在接受EKI-785治疗的动物中观察到肾cAMP和血管加压素V2受体表达增加。
EGFR酪氨酸激酶抑制不能保护PCK大鼠免于PKD的发展。这可能是由于对集合管cAMP的影响抵消了对细胞外调节蛋白激酶(ERK)/丝裂原活化蛋白激酶(MAPK)途径可能的有益作用,特别是在没有EGFR过表达或错位的情况下。这些观察结果与人类囊性肾病治疗的相关性值得进一步研究。