The Mg2+ transporter MagT1 partially rescues cell growth and Mg2+ uptake in cells lacking the channel-kinase TRPM7.

Abstract:

:Magnesium (Mg(2+)) transport across membranes plays an essential role in cellular growth and survival. TRPM7 is the unique fusion of a Mg(2+) permeable pore with an active cytosolic kinase domain, and is considered a master regulator of cellular Mg(2+) homeostasis. We previously found that the genetic deletion of TRPM7 in DT40 B cells results in Mg(2+) deficiency and severe growth impairment, which can be rescued by supplementation with excess extracellular Mg(2+). Here, we show that gene expression of the Mg(2+) selective transporter MagT1 is upregulated in TRPM7(-/-) cells. Furthermore, overexpression of MagT1 in TRPM7(-/-) cells augments their capacity to uptake Mg(2+), and improves their growth behavior in the absence of excess Mg(2+).

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Deason-Towne F,Perraud AL,Schmitz C

doi

10.1016/j.febslet.2011.05.052

subject

Has Abstract

pub_date

2011-07-21 00:00:00

pages

2275-8

issue

14

eissn

0014-5793

issn

1873-3468

pii

S0014-5793(11)00418-2

journal_volume

585

pub_type

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