Science and Research

Mg(2+) Supplementation Mitigates Metabolic Deficits Associated With TRPM7 Disruption

Transient receptor potential channel subfamily M member 7 (TRPM7) regulates cellular and systemic Mg(2+) homeostasis through its channel domain and induces protein phosphorylation via its kinase domain. We recently found that mice with selective deletion of Trpm7 in

  • Boulassel, S.
  • Schreier, P. C. F.
  • Melyshi, A. M.
  • Berger, J.
  • Reinach, P. S.
  • Jacob, K.
  • Boekhoff, I.
  • Breit, A.
  • Müller, T. D.
  • Zierler, S.
  • Gudermann, T.
  • Khajavi, N.

Keywords

  • Animals
  • *TRPM Cation Channels/genetics/metabolism/deficiency
  • *Magnesium/pharmacology
  • Insulin-Secreting Cells/metabolism/drug effects
  • Mice
  • Cell Proliferation/drug effects
  • *Protein Serine-Threonine Kinases/genetics/metabolism
  • Dietary Supplements
  • Insulin/metabolism
  • *Glucose Intolerance/genetics/metabolism/drug therapy
  • Insulin Secretion/drug effects
  • Male
  • Insulin Resistance
  • Mice, Knockout
  • Diet, High-Fat
  • Mice, Inbred C57BL
  • Phosphorylation
  • Homeodomain Proteins/metabolism/genetics
  • Trans-Activators
  • Mg2+ supplementation
  • Trpm7
  • glucose metabolism
  • pancreatic β‐cell
  • proliferation
Publication details
DOI: 10.1002/jcp.70042
Journal: J Cell Physiol
Pages: e70042 
Number: 4
Work Type: Original
Location: CPC-M
Disease Area: General Lung and Other
Partner / Member: LMU
Access-Number: 40275767


chevron-down