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Molecular Bases of Disease
2 Results
- JBC ReviewsOpen Access
Brain manganese and the balance between essential roles and neurotoxicity
Journal of Biological ChemistryVol. 295Issue 19p6312–6329Published online: March 18, 2020- Rekha C. Balachandran
- Somshuvra Mukhopadhyay
- Danielle McBride
- Jennifer Veevers
- Fiona E. Harrison
- Michael Aschner
- and others
Cited in Scopus: 91Manganese (Mn) is an essential micronutrient required for the normal development of many organs, including the brain. Although its roles as a cofactor in several enzymes and in maintaining optimal physiology are well-known, the overall biological functions of Mn are rather poorly understood. Alterations in body Mn status are associated with altered neuronal physiology and cognition in humans, and either overexposure or (more rarely) insufficiency can cause neurological dysfunction. The resultant balancing act can be viewed as a hormetic U-shaped relationship for biological Mn status and optimal brain health, with changes in the brain leading to physiological effects throughout the body and vice versa. - Molecular Bases of DiseaseOpen Access
Hypothyroidism induced by loss of the manganese efflux transporter SLC30A10 may be explained by reduced thyroxine production
Journal of Biological ChemistryVol. 292Issue 40p16605–16615Published online: August 31, 2017- Chunyi Liu
- Steven Hutchens
- Thomas Jursa
- William Shawlot
- Elena V. Polishchuk
- Roman S. Polishchuk
- and others
Cited in Scopus: 37SLC30A10 and SLC39A14 are manganese efflux and influx transporters, respectively. Loss-of-function mutations in genes encoding either transporter induce hereditary manganese toxicity. Patients have elevated manganese in the blood and brain and develop neurotoxicity. Liver manganese is increased in patients lacking SLC30A10 but not SLC39A14. These organ-specific changes in manganese were recently recapitulated in knockout mice. Surprisingly, Slc30a10 knockouts also had elevated thyroid manganese and developed hypothyroidism.