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10.1038/cddis.2015.39

http://scihub22266oqcxt.onion/10.1038/cddis.2015.39
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C4385918!4385918!25766322
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suck abstract from ncbi


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pmid25766322      Cell+Death+Dis 2015 ; 6 (3): e1683-
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  • Plasma membrane poration by opioid neuropeptides: a possible mechanism of pathological signal transduction #MMPMID25766322
  • Maximyuk O; Khmyz V; Lindskog CJ; Vukojevi? V; Ivanova T; Bazov I; Hauser KF; Bakalkin G; Krishtal O
  • Cell Death Dis 2015[Mar]; 6 (3): e1683- PMID25766322show ga
  • Neuropeptides induce signal transduction across the plasma membrane by acting through cell-surface receptors. The dynorphins, endogenous ligands for opioid receptors, are an exception; they also produce non-receptor-mediated effects causing pain and neurodegeneration. To understand non-receptor mechanism(s), we examined interactions of dynorphins with plasma membrane. Using fluorescence correlation spectroscopy and patch-clamp electrophysiology, we demonstrate that dynorphins accumulate in the membrane and induce a continuum of transient increases in ionic conductance. This phenomenon is consistent with stochastic formation of giant (~2.7?nm estimated diameter) unstructured non-ion-selective membrane pores. The potency of dynorphins to porate the plasma membrane correlates with their pathogenic effects in cellular and animal models. Membrane poration by dynorphins may represent a mechanism of pathological signal transduction. Persistent neuronal excitation by this mechanism may lead to profound neuropathological alterations, including neurodegeneration and cell death.
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