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Published on: December 9, 2022
Opening/blocking actions of pyruvate kinase antibodies on neuronal and muscular KATP channels
Antonietta Mele1, Maura Buttiglione, Gianluigi Cannone
1Unit of Pharmacology, Department of Pharmacy, via Orabona no. 4, University of Bari, I-70126 Bari, Italy.
Insights
Autoantibodies against pyruvate kinase (PK) impact ATP-sensitive potassium (KATP) channels. Short-term exposure enhances KATP currents, while long-term exposure causes atrophy and neuronal death, suggesting a novel therapeutic target for autoimmune diseases.
Area of Science:
- Cellular physiology
- Neuroscience
- Immunology
Background:
- ATP-sensitive potassium (KATP) channels link cellular metabolism to electrical activity.
- Pyruvate kinase (PK) is implicated in PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders) due to autoantibody production.
- The interaction between PK and KATP channels in muscle and neurons is not fully understood.
Purpose of the Study:
- To investigate the effects of anti-pyruvate kinase antibodies (anti-PK-ab) on muscle and neuronal KATP channels.
- To explore the physical and functional coupling between PK and KATP channel subunits (Kir6.1/Kir6.2).
- To assess the potential of the KATP/PK complex as a therapeutic target in autoimmune diseases.
Main Methods:
- Patch-clamp electrophysiology on rat skeletal muscle fibers and human neuroblastoma cell lines (SH-SY5Y).
- Co-immunoprecipitation experiments in mouse brain to investigate protein interactions.
- Short-term (1h) and long-term (24h) incubations with anti-PK-ab at varying dilutions.
Main Results:
- Short-term anti-PK-ab exposure enhanced KATP currents in muscle fibers (up to 33.5%) and potentiated neuronal KATP currents without affecting survival.
- Long-term anti-PK-ab exposure reduced muscle KATP currents (up to 24%), induced fiber atrophy, and caused neuronal death by reducing KATP currents.
- Direct application of anti-PK-ab blocked KATP channels without ATP but opened them in the presence of ATP, demonstrating functional coupling between PK and Kir subunits in neurons.
Conclusions:
- Anti-PK antibodies exert dual effects on KATP channels, with short-term exposure enhancing and long-term exposure inhibiting channel activity, leading to cellular damage.
- PK and KATP channel subunits (Kir) are physically and functionally coupled in neurons.
- The KATP/PK complex represents a potential novel therapeutic target for autoimmune conditions associated with anti-PK antibodies, such as PANDAS.
Abstract:
ATP-sensitive-K(+) (KATP) channels couple metabolism to the electrical activity of the cells. This channel is associated with glycolytic enzymes to form complexes regulating the channel activity in various tissues. The pyruvate-kinase (PK) enzyme is an antigen in the Paediatric Autoimmune Neuropsychiatric Disorders Associated Streptococcal infection known as PANDAS which is characterized by an abnormal production of auto-antibodies against PK. Here, the effects of the anti-pyruvate kinase antibody (anti-PK-ab) on the muscle and neuronal KATP channels were investigated in native rat skeletal muscle fibres and human neuroblastoma cell-line (SH-SY5Y), respectively. Furthermore, the interaction of PK with the inwardly rectifier potassium channel (Kir6.1/Kir6.2) subunits of the KATP channels was investigated by co-immunoprecipitation experiments in mouse brain using the anti-PK-ab. Patch-clamp experiments showed that the short-term incubation (1h) of the fibres with the anti-PK-ab at the dilutions of 1:500 and 1:300 enhanced the KATP current of 19.6% and 33.5%, respectively. As opposite, the long-term incubation (24h) of the fibres with the anti-PK-ab at the dilutions of 1:500 and 1:300 reduced the KATP current of 16% and 24%, respectively, reducing the diameter with atrophy. The direct application of the anti-PK-ab to the excised patches in the absence of intracellular ATP caused channel block, while in the presence of nucleotide channel opened. In neuronal cell line, in the short-term the anti-PK-ab potentiated KATP currents without affecting survival, while in the long-term the anti-PK-ab reduced KATP currents inducing neuronal death. Opening/blocking actions of the anti-PK antibodies on the KATP channels were observed, the blocking action causes fibre atrophy and neuronal death. We demonstrated that PK and Kir subunits are physically/functionally coupled in neurons. The KATP/PK complex can be proposed a novel target in the autoimmune diseases associated with anti-PK production as in PANDAS.
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