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.

Pharmacological Research
|September 13, 2012
PubMed

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.

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