Endothelial ZIP8 plays a minor role in BMP6 regulation by iron in mice

被引:4
|
作者
Fisher, Allison L. [1 ,2 ]
Phillips, Sydney [1 ,2 ]
Wang, Chia-Yu [1 ,2 ]
Paulo, Joao A. [3 ]
Xiao, Xia [1 ,2 ]
Moschetta, Gillian A. [1 ,2 ]
Sridhar, Adhvaith [1 ,2 ]
Mancias, Joseph D. [4 ]
Babitt, Jodie L. [1 ,2 ,5 ,6 ]
机构
[1] Massachusetts Gen Hosp, Nephrol Div, Boston, MA USA
[2] Massachusetts Gen Hosp, Endocrine Unit, Boston, MA USA
[3] Harvard Med Sch, Dept Cell Biol, Boston, MA 02114 USA
[4] Harvard Med Sch, Dana Farber Canc Inst, Dept Radiat Oncol, Div Radiat & Genome Stabil, Boston, MA 02114 USA
[5] Harvard Med Sch, Massachusetts Gen Hosp, Nephrol Div, Thier Res Bldg 1123A,50 Blossom St, Boston, MA 02114 USA
[6] Harvard Med Sch, Massachusetts Gen Hosp, Endocrine Unit, Thier Res Bldg 1123A,50 Blossom St, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
LIVER; HOMEOSTASIS; EXPRESSION; OVERLOAD; SERUM;
D O I
10.1182/blood.2023023385
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Iron-mediated induction of bone morphogenetic protein (BMP)6 expression by liver endothelial cells is essential for iron homeostasis regulation. We used multiple dietary and genetic mouse cohorts to demonstrate a minor functional role for the metal-ion transporter ZIP8 in regulating BMP6 expression under high-iron conditions.
引用
收藏
页码:2433 / 2437
页数:5
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