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Regulation of Kv2.1 channel inactivation by phosphatidylinositol 4,5-bisphosphate.
Delgado-Ramírez, Mayra; De Jesús-Pérez, José J; Aréchiga-Figueroa, Iván A; Arreola, Jorge; Adney, Scott K; Villalba-Galea, Carlos A; Logothetis, Diomedes E; Rodríguez-Menchaca, Aldo A.
Afiliação
  • Delgado-Ramírez M; Departamento de Fisiología y Biofísica, Facultad de Medicina, Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP 78210, Mexico.
  • De Jesús-Pérez JJ; Instituto de Física, Universidad Autónoma de San Luis Potosí, Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP 78290, Mexico.
  • Aréchiga-Figueroa IA; CONACYT, Facultad de Medicina, Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP 78210, Mexico.
  • Arreola J; Instituto de Física, Universidad Autónoma de San Luis Potosí, Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP 78290, Mexico.
  • Adney SK; Department of Physiology and Biophysics, Virginia Commonwealth University School of Medicine, Richmond, VA, 23298, USA.
  • Villalba-Galea CA; Department of Neurology, Northwestern University, Chicago, IL, 60611, USA.
  • Logothetis DE; Department of Physiology and Pharmacology, Thomas J. Long School of Pharmacy & Health Sciences, University of the Pacific, Stockton, CA, 95211, USA.
  • Rodríguez-Menchaca AA; Department of Physiology and Biophysics, Virginia Commonwealth University School of Medicine, Richmond, VA, 23298, USA. d.logothetis@northeastern.edu.
Sci Rep ; 8(1): 1769, 2018 01 29.
Article em En | MEDLINE | ID: mdl-29379118
Phosphatidylinositol 4,5-bisphosphate (PIP2) is a membrane phospholipid that regulates the function of multiple ion channels, including some members of the voltage-gated potassium (Kv) channel superfamily. The PIP2 sensitivity of Kv channels is well established for all five members of the Kv7 family and for Kv1.2 channels; however, regulation of other Kv channels by PIP2 remains unclear. Here, we investigate the effects of PIP2 on Kv2.1 channels by applying exogenous PIP2 to the cytoplasmic face of excised membrane patches, activating muscarinic receptors (M1R), or depleting endogenous PIP2 using a rapamycin-translocated 5-phosphatase (FKBP-Inp54p). Exogenous PIP2 rescued Kv2.1 channels from rundown and partially prevented the shift in the voltage-dependence of inactivation observed in inside-out patch recordings. Native PIP2 depletion by the recruitment of FKBP-Insp54P or M1R activation in whole-cell experiments, induced a shift in the voltage-dependence of inactivation, an acceleration of the closed-state inactivation, and a delayed recovery of channels from inactivation. No significant effects were observed on the activation mechanism by any of these treatments. Our data can be modeled by a 13-state allosteric model that takes into account that PIP2 depletion facilitates inactivation of Kv2.1. We propose that PIP2 regulates Kv2.1 channels by interfering with the inactivation mechanism.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfatidilinositol 4,5-Difosfato / Canais de Potássio Shab Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfatidilinositol 4,5-Difosfato / Canais de Potássio Shab Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido