高铁与低铁环境对成骨细胞hFOB1.19膜铁转运蛋白1表达的影响

被引:3
作者
赵国阳 [1 ]
张伟 [1 ]
何银锋 [1 ]
李光飞 [1 ]
林华 [2 ]
徐又佳 [1 ]
机构
[1] 苏州大学附属第二医院骨科
[2] 南京大学医学院附属鼓楼医院骨病中心
关键词
成骨细胞; 铁代谢; 膜铁转运蛋白;
D O I
暂无
中图分类号
R363 [病理生理学];
学科分类号
100103 [病原生物学];
摘要
目的观察细胞培养液中加入铁离子或铁离子螯合剂后成骨细胞(hFOB1.19)膜铁转运蛋白1(FPN1)表达的变化,探讨铁离子浓度对成骨细胞FPN1表达的影响。方法将不同浓度的枸橼酸铁铵(FAC,50、100、200μmol/L)和去铁胺(DFO,5、10、20μmol/L)分别加入人hFOB1.19培养基,24h后用共聚焦显微镜(CLSM)测定细胞内铁离子浓度,用定量PCR、Westernblotting和免疫荧光法测定不同组别成骨细胞FPN1的表达并进行统计比较。结果用不同浓度的FAC和DFO干预20h后,成骨细胞内铁离子浓度随FAC浓度增加而增加,随DFO浓度增加而降低,组间差异有统计学意义(P<0.05);FPN1基因和蛋白表达随FAC浓度增加而增加,随DFO浓度增加而降低,组间差异有统计学意义(P<0.05)。结论高铁环境可上调FPN1表达,低铁环境可下调FPN1表达。FPN1表达量的改变可有效维持成骨细胞内铁离子浓度的平衡。
引用
收藏
页码:264 / 270
页数:7
相关论文
共 17 条
[1]
Iron homeostasis in osteoporosis and its clinical implications [J].
Li, G. F. ;
Pan, Y. Z. ;
Sirois, P. ;
Li, K. ;
Xu, Y. J. .
OSTEOPOROSIS INTERNATIONAL, 2012, 23 (10) :2403-2408
[2]
Nrf2 regulates ferroportin 1-mediated iron efflux and counteracts lipopolysaccharide-induced ferroportin 1 mRNA suppression in macrophages [J].
Harada, Nobuhiko ;
Kanayama, Masaya ;
Maruyama, Atsushi ;
Yoshida, Aruto ;
Tazumi, Kyoko ;
Hosoya, Tomonori ;
Mimura, Junsei ;
Toki, Tsutomu ;
Maher, Jonathan M. ;
Yamamoto, Masayuki ;
Itoh, Ken .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2011, 508 (01) :101-109
[3]
Iron chelator deferoxamine alters iron-regulatory genes and proteins and suppresses osteoblast phenotype in fetal rat calvaria cells [J].
Messer, Jonathan G. ;
Cooney, Paula T. ;
Kipp, Deborah E. .
BONE, 2010, 46 (05) :1408-1415
[4]
Iron overload alters iron-regulatory genes and proteins, down-regulates osteoblastic phenotype, and is associated with apoptosis in fetal rat calvaria cultures [J].
Messer, Jonathan G. ;
Kilbarger, Amy K. ;
Erikson, Keith M. ;
Kipp, Deborah E. .
BONE, 2009, 45 (05) :972-979
[5]
Excess iron inhibits osteoblast metabolism.[J].Kanako Yamasaki;Hiromi Hagiwara.Toxicology Letters.2009, 2
[6]
Differing expression of genes involved in non-transferrin iron transport across plasma membrane in various cell types under iron deficiency and excess [J].
Kamila Balusikova ;
Jitka Neubauerova ;
Marketa Dostalikova-Cimburova ;
Jiri Horak ;
Jan Kovar .
Molecular and Cellular Biochemistry, 2009, 321 :123-133
[7]
Therapeutic Effects of an Oral Chelator Targeting Skeletal Tissue Damage in Experimental Postmenopausal Osteoporosis in Rats*.[J].Gang Liu;Ping Men;Gerry H. Kenner;Scott C. Miller.Hemoglobin.2008, 1-2
[8]
Age-associated iron accumulation in bone: Implications for postmenopausal osteoporosis and a new target for prevention and treatment by chelation [J].
Liu, Gang ;
Men, Ping ;
Kenner, Gerry H. ;
Miller, Scott C. .
BIOMETALS, 2006, 19 (03) :245-251
[9]
Iron loading: a risk factor for osteoporosis [J].
Weinberg, E. D. .
BIOMETALS, 2006, 19 (06) :633-635
[10]
Iron restriction negatively affects bone in female rats and mineralization of hFOB osteoblast cells [J].
Parelman, M ;
Stoecker, B ;
Baker, A ;
Medeiros, D .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2006, 231 (04) :378-386