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Pei Jin Lim

DPhil Student

I am interested in the molecular mechanisms regulating iron homeostasis. I study how the body senses excess iron and converts that into a danger signal to regulate iron absorption. Our work shows that the transcription factor Nrf2, the master regulator of antioxidant response, is a molecular sensor of iron that upregulates the Bmp/Smad signalling pathway to induce hepcidin synthesis and block further iron uptake and recycling. Nrf2-deficiency causes defective Bmp6 and hepcidin responses, and causes iron over-accumulation. In haemochromatosis patients, a SNP in the NRF2 promoter is predicted to reduce NRF2 activity and is associated with increased disease burden. Pharmacological activation of Nrf2 rescues iron accumulation in a haemochromatosis mouse model. These findings may translate into new therapeutic options for treating iron overload diseases via activating Nrf2.

Before my DPhil, I did my B.Sc degree at the University of Singapore. I studied the replication of Chikungunya virus at the Department of Microbiology in the lab of Dr Justin Chu. I came to Oxford in 2013 and joined the Drakesmith lab as a DPhil student.

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Latest Publications


Lim PJ. et al, (2017), AMERICAN JOURNAL OF HEMATOLOGY, 92, E189 - E189

Hepcidin is regulated by promoter-associated histone acetylation and HDAC3

Pasricha SR. et al, (2017), Nat Commun, 8

Induced Disruption of the Iron-Regulatory Hormone Hepcidin Inhibits Acute Inflammatory Hypoferraemia.

Armitage AE. et al, (2016), J Innate Immun, 8, 517 - 528