Hada Hiroshi, Shiraki Takuma, Watanabe-Matsui Miki, Igarashi Kazuhiko
Department of Biochemistry, and Center for Regulatory Epigenome and Disease, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan; CREST, Japan Science and Technology Agency, Sendai 980-8575, Japan.
Faculty of Biology-Oriented Science and Technology, Kinki University, Nishimitani, Kinokawashi, Wakayama 649-6493, Japan.
Biochim Biophys Acta. 2014 Jul;1840(7):2351-60. doi: 10.1016/j.bbagen.2014.02.029. Epub 2014 Mar 5.
Intracellular heme plays versatile roles in a variety of physiological processes including mitochondrial respiration. Heme also induces the expression of genes such as heme oxygenase-1 (HO-1) by inactivating the transcription repressor Bach1 through direct binding. However, the source of heme for the regulation of the Bach1-HO-1 axis has been unclear. Considering that extracellular heme exists as a complex with hemopexin (Hx) in serum under the physiological conditions, heme-Hx complex may deliver heme for the gene regulation.
Using a mammalian expression system, high secretory recombinant Hx (rHx) was developed. We examined the effects of rHx-bound heme on HO-1 expression and Bach1 in Hepa-1c1c7 liver cells and THP-1 macrophage cells. We investigated the uptake pathway of rHx-bound heme by treating cells with chlorpromazine (CPZ).
rHx-bound heme induced the expression of HO-1 and decreased the level of Bach1 protein. CPZ inhibited the induction of the HO-1 expression by rHx-bound heme.
rHx-bound heme was internalized into the cells via endocytosis, resulting in HO-1 expression and inactivation of Bach1.
The Bach1-dependent repression of the HO-1 expression is under the control of the Hx-dependent uptake of extracellular heme. Heme may regulate Bach1 as an extracellular signaling molecule.
细胞内血红素在包括线粒体呼吸在内的多种生理过程中发挥着多种作用。血红素还通过直接结合使转录抑制因子Bach1失活,从而诱导血红素加氧酶-1(HO-1)等基因的表达。然而,调节Bach1-HO-1轴的血红素来源尚不清楚。考虑到在生理条件下,细胞外血红素在血清中与血红素结合蛋白(Hx)形成复合物,血红素-Hx复合物可能为基因调控传递血红素。
利用哺乳动物表达系统,开发了高分泌性重组Hx(rHx)。我们检测了rHx结合的血红素对Hepa-1c1c7肝细胞和THP-1巨噬细胞中HO-1表达和Bach1的影响。我们通过用氯丙嗪(CPZ)处理细胞来研究rHx结合的血红素的摄取途径。
rHx结合的血红素诱导HO-1的表达,并降低Bach1蛋白水平。CPZ抑制rHx结合的血红素对HO-1表达的诱导。
rHx结合的血红素通过内吞作用内化到细胞中,导致HO-1表达和Bach1失活。
HO-1表达的Bach1依赖性抑制受细胞外血红素的Hx依赖性摄取的控制。血红素可能作为一种细胞外信号分子调节Bach1。