Anti-Kir4.1 Antibodies in Multiple Sclerosis: Specificity and Pathogenicity.
Michie ImamuraOsamu HiguchiYasuhiro MaedaAkihiro MukainoMitsuharu UedaHidenori MatsuoShunya NakanePublished in: International journal of molecular sciences (2020)
The glial cells in the central nervous system express diverse inward rectifying potassium channels (Kir). They express multiple Kir channel subtypes that are likely to have distinct functional roles related to their differences in conductance, and sensitivity to intracellular and extracellular factors. Dysfunction in a major astrocyte potassium channel, Kir4.1, appears as an early pathological event underlying neuronal phenotypes in several neurological diseases. The autoimmune effects on the potassium channel have not yet been fully described in the literature. However, several research groups have reported that the potassium channels are an immune target in patients with various neurological disorders. In 2012, Srivastava et al. reported about Kir4.1, a new immune target for autoantibodies in patients with multiple sclerosis (MS). Follow-up studies have been conducted by several research groups, but no clear conclusion has been reached. Most follow-up studies, including ours, have reported that the prevalence of Kir4.1-seropositive patients with MS was lower than that in the initial study. Therefore, we extensively review studies on the method of antibody testing, seroprevalence of MS, and other neurological diseases in patients with MS. Finally, based on the role of Kir4.1 in MS, we consider whether it could be an immune target in this disease.
Keyphrases
- multiple sclerosis
- mass spectrometry
- ms ms
- case control
- systematic review
- induced apoptosis
- oxidative stress
- spinal cord injury
- risk factors
- spinal cord
- cell proliferation
- staphylococcus aureus
- cell death
- subarachnoid hemorrhage
- cell cycle arrest
- endoplasmic reticulum stress
- cerebrospinal fluid
- blood brain barrier
- pseudomonas aeruginosa