Oulu Center for Cell-Matrix Research, Biocenter Oulu, Finland.
Blood. 2012 Oct 18;120(16):3336-44. doi: 10.1182/blood-2012-07-441824. Epub 2012 Sep 5.
An endoplasmic reticulum transmembrane prolyl 4-hydroxylase (P4H-TM) is able to hydroxylate the α subunit of the hypoxia-inducible factor (HIF) in vitro and in cultured cells, but nothing is known about its roles in mammalian erythropoiesis. We studied such roles here by administering a HIF-P4H inhibitor, FG-4497, to P4h-tm(-/-) mice. This caused larger increases in serum Epo concentration and kidney but not liver Hif-1α and Hif-2α protein and Epo mRNA levels than in wild-type mice, while the liver Hepcidin mRNA level was lower in the P4h-tm(-/-) mice than in the wild-type. Similar, but not identical, differences were also seen between FG-4497-treated Hif-p4h-2 hypomorphic (Hif-p4h-2(gt/gt)) and Hif-p4h-3(-/-) mice versus wild-type mice. FG-4497 administration increased hemoglobin and hematocrit values similarly in the P4h-tm(-/-) and wild-type mice, but caused higher increases in both values in the Hif-p4h-2(gt/gt) mice and in hematocrit value in the Hif-p4h-3(-/-) mice than in the wild-type. Hif-p4h-2(gt/gt)/P4h-tm(-/-) double gene-modified mice nevertheless had increased hemoglobin and hematocrit values without any FG-4497 administration, although no such abnormalities were seen in the Hif-p4h-2(gt/gt) or P4h-tm(-/-) mice. Our data thus indicate that P4H-TM plays a role in the regulation of EPO production, hepcidin expression, and erythropoiesis.
内质网跨膜脯氨酰 4-羟化酶(P4H-TM)能够在体外和培养细胞中使缺氧诱导因子(HIF)的α亚基羟化,但对于其在哺乳动物红细胞生成中的作用尚不清楚。我们通过给 P4h-tm(-/-) 小鼠施用 HIF-P4H 抑制剂 FG-4497 来研究其在红细胞生成中的作用。这导致血清 Epo 浓度和肾脏而非肝脏 Hif-1α 和 Hif-2α 蛋白和 Epo mRNA 水平的增加大于野生型小鼠,而 P4h-tm(-/-) 小鼠的肝脏 Hepcidin mRNA 水平低于野生型。在 FG-4497 处理的 Hif-p4h-2 低功能(Hif-p4h-2(gt/gt))和 Hif-p4h-3(-/-) 小鼠与野生型小鼠之间也观察到类似但不完全相同的差异。FG-4497 给药同样增加 P4h-tm(-/-) 和野生型小鼠的血红蛋白和血细胞比容值,但在 Hif-p4h-2(gt/gt) 小鼠中增加了这两个值,在 Hif-p4h-3(-/-) 小鼠中增加了血细胞比容值。然而,Hif-p4h-2(gt/gt)/P4h-tm(-/-) 双基因修饰小鼠即使没有 FG-4497 给药也会增加血红蛋白和血细胞比容值,而在 Hif-p4h-2(gt/gt) 或 P4h-tm(-/-) 小鼠中则没有观察到这种异常。因此,我们的数据表明 P4H-TM 在调节 EPO 产生、hepcidin 表达和红细胞生成中发挥作用。