Nesbitt T, Drezner M K
Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA.
Am J Physiol. 1997 Jul;273(1 Pt 2):F113-9. doi: 10.1152/ajprenal.1997.273.1.F113.
Although current theory holds that the murine homologs of X-linked hypophosphatemia represent mutations of two closely linked genes with distinct pathophysiological consequences, insufficient data are available to support this hypothesis. We investigated whether an intrinsic defect in renal sodium (Na+)-dependent Pi cotransport truly distinguishes gy from hyp mice. We compared Pi transport in immortalized cells from S1 and S2 segments of the renal proximal convoluted tubule (PCT) of normal and gy mice. Cells from both murine models exhibit characteristics of differentiated PCT cells including gluconeogenesis, alkaline phosphatase activity, and parathyroid hormone (PTH)- and thyrocalcitonin (TCT)-dependent adenosine 3',5'-cyclic monophosphate production. More importantly, kinetic studies reveal that cells from the PCT of gy mice have intrinsically normal Pi transport and support the hypothesis that, as in hyp mice, a humoral abnormality is likely responsible for the renal Pi wasting in this mouse model. These observations are consistent with the conclusion that gy and hyp mice do not represent mutations of two closely linked genes but rather two separate mutations of the same gene.
尽管目前的理论认为,X连锁低磷血症的小鼠同源基因代表两个紧密连锁基因的突变,具有不同的病理生理后果,但尚无足够的数据支持这一假说。我们研究了肾钠(Na+)依赖性磷共转运的内在缺陷是否真的能区分gy小鼠和hyp小鼠。我们比较了正常小鼠和gy小鼠肾近端曲管(PCT)S1和S2段永生化细胞中的磷转运。两种小鼠模型的细胞均表现出分化的PCT细胞的特征,包括糖异生、碱性磷酸酶活性以及甲状旁腺激素(PTH)和甲状腺降钙素(TCT)依赖性环磷酸腺苷的产生。更重要的是,动力学研究表明,gy小鼠PCT的细胞具有内在正常的磷转运,并支持这样的假说,即与hyp小鼠一样,体液异常可能是该小鼠模型中肾性磷消耗的原因。这些观察结果与以下结论一致,即gy小鼠和hyp小鼠并不代表两个紧密连锁基因的突变,而是同一基因的两个独立突变。