Citation

BibTex format

@article{Zhao:2015:10.1038/nature14620,
author = {Zhao, L and Oliver, E and Maratou, K and Atanur, SS and Dubois, OD and Cotroneo, E and Chen, CN and Wang, L and Arce, C and Chabosseau, PL and Ponsa-Cobas, J and Frid, MG and Moyon, B and Webster, Z and Aldashev, A and Ferrer, J and Rutter, GA and Stenmark, KR and Aitman, TJ and Wilkins, MR},
doi = {10.1038/nature14620},
journal = {Nature},
pages = {356--360},
title = {The zinc transporter, ZIP12, regulates the pulmonary vascular response to chronic hypoxia},
url = {http://dx.doi.org/10.1038/nature14620},
volume = {524},
year = {2015}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - The typical response of the adult mammalian pulmonary circulation to a low oxygen environment is vasoconstriction and structural remodelling of pulmonary arterioles, leading to chronic elevation of pulmonary artery pressure (pulmonary hypertension) and right ventricular hypertrophy. Some mammals, however, exhibit genetic resistance to hypoxia-induced pulmonary hypertension1, 2, 3. We used a congenic breeding program and comparative genomics to exploit this variation in the rat and identified the gene Slc39a12 as a major regulator of hypoxia-induced pulmonary vascular remodelling. Slc39a12 encodes the zinc transporter ZIP12. Here we report that ZIP12 expression is increased in many cell types, including endothelial, smooth muscle and interstitial cells, in the remodelled pulmonary arterioles of rats, cows and humans susceptible to hypoxia-induced pulmonary hypertension. We show that ZIP12 expression in pulmonary vascular smooth muscle cells is hypoxia dependent and that targeted inhibition of ZIP12 inhibits the rise in intracellular labile zinc in hypoxia-exposed pulmonary vascular smooth muscle cells and their proliferation in culture. We demonstrate that genetic disruption of ZIP12 expression attenuates the development of pulmonary hypertension in rats housed in a hypoxic atmosphere. This new and unexpected insight into the fundamental role of a zinc transporter in mammalian pulmonary vascular homeostasis suggests a new drug target for the pharmacological management of pulmonary hypertension.
AU - Zhao,L
AU - Oliver,E
AU - Maratou,K
AU - Atanur,SS
AU - Dubois,OD
AU - Cotroneo,E
AU - Chen,CN
AU - Wang,L
AU - Arce,C
AU - Chabosseau,PL
AU - Ponsa-Cobas,J
AU - Frid,MG
AU - Moyon,B
AU - Webster,Z
AU - Aldashev,A
AU - Ferrer,J
AU - Rutter,GA
AU - Stenmark,KR
AU - Aitman,TJ
AU - Wilkins,MR
DO - 10.1038/nature14620
EP - 360
PY - 2015///
SN - 0028-0836
SP - 356
TI - The zinc transporter, ZIP12, regulates the pulmonary vascular response to chronic hypoxia
T2 - Nature
UR - http://dx.doi.org/10.1038/nature14620
UR - http://hdl.handle.net/10044/1/31147
VL - 524
ER -
Faculty of MedicineDepartment of Metabolism, Digestion and Reproduction

General enquiries


Beta Cell Genome Regulation Lab
ICTEM Building, 5th floor
Hammersmith Campus
Du Cane Road
London
W12 0NN

Enquiries
d.cieslak-jones@imperial.ac.uk
+44 (0)20 7594 2739