TRPM7 channel-kinase in immunity: new frontiers of an emerging therapeutic target
The cation channel and protein kinase transient receptor potential cation channel subfamily M member 7 (TRPM7) has been linked to immune homeostasis, immune cell signaling and differentiation, and inflammatory diseases. Its importance in guiding ion-mediated cellular responses, funneling discrete kinase signal transduction events, and contributing to complex membrane-localized protein networks positions the channel-kinase as a promising pharmacological target. Diseases with underlying exacerbation of ion-coupled cellular responses are in focus. Undoubtedly, the manifold cells of the immune system undertake a key position in their demand for a smoothly adaptable molecular performance, reacting to incorporate environmental and nutritional triggers to guide diverse cellular states. We here discuss a current view of the molecular principles underlying TRPM7 function in immunity and provide a grasping outlook on open questions and research topics we expect to emerge in the upcoming years, positioning TRPM7 as an unattended player at the forefront of immune regulation.
Authors
- Birgit Hoeger (ORCID: https://orcid.org/0000-0001-7491-9405)
- Anna Madlmayr (ORCID: https://orcid.org/0000-0002-4518-147X)
- Susanna Zierler (ORCID: https://orcid.org/0000-0002-4684-0385)
Institutions
- Johannes Kepler University of Linz (AT)
- Ludwig-Maximilians-Universität München (DE)
Publication Details
- Journal
- Current Opinion in Immunology
- Published
- 2026-02-13
- DOI
- https://doi.org/10.1016/j.coi.2026.102734
- Primary Topic
- Magnesium in Health and Disease
- Type
- article
- Field-Weighted Citation Impact
- 0.00