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Biology subjects

Herold, K. F.

Publications and source records attributed to Herold, K. F..

5 recordsLinked to original sources

Genetically engineered rapamycin responsive K2P channels

Establishment of electrical potentials across biological membranes is a universal feature of all cells. Tandem pore domain (K2P) potassium ion channels play pivotal roles in maintaining cellular membrane potentials, shaping physiological responses across a diverse range of cell types. With only a limited repertoire of high-aAinity and subtype-selective K2P modulators available for experimental or therapeutic use, we devised a strategy to genetically engineer K2P channels that are potently activated by rapamycin or non-immunomodulatory rapamycin analogs. Insertion of the FRB domain of mTOR into a short flexible cytoplasmic loop between the second and third transmembrane (TM) domains of the TREK1 K2P channel yielded fusion channels that are activated by nanomolar concentrations of rapamycin. Rapamycin-induced potentiation requires recruitment of an FKBP binding partner, from either the endogenous pool of FKBP within the cell or through fusion of FKBP to the C-terminus of TREK1. Formation of an FRB/rapamycin/FKBP ternary complex within the core of the TREK1 channel leads to an increase in TREK1 single-channel open probability and unitary current, mimicking positive modulatory eAects of conventional TREK1 activating cues. Cryo-EM structures demonstrate that rapamycin-induced ternary complex formation rigidifies the position of the FRB and stabilizes the TM2/TM3 loop in an active channel conformation. We demonstrate that FRB fusion can be employed to successfully activate several K2P channel isoforms, providing chemogenetically targetable tools for direct manipulation of cellular membrane potential.

bioengineering↗

Presynaptic NMDA receptors on mouse mossy fiber terminals mediate rapid BDNF release by ketamine and hydroxynorketamine

Major depressive disorder is associated with deficits in hippocampal synaptic plasticity that depend on brain-derived neurotrophic factor (BDNF) release from both axonal and dendritic compartments. Antidepressant efficacy requires enhanced BDNF signaling, thought to be mediated by drug-induced BDNF release from postsynaptic dendritic spines. Here, we show that fast-acting antidepressants rapidly trigger BDNF secretion from presynaptic terminals in hippocampal area CA3. At antidepressant-relevant concentrations, ketamine and its metabolite (2R,6R)-hydroxynorketamine (HNK) induced BDNF release within minutes from mossy fiber terminals of dentate granule neurons in rat hippocampal cultures, with no detectable secretion from dendritic spines. This antidepressant-evoked BDNF release required presynaptic NMDA receptors (preNMDARs). Conditional genetic deletion of preNMDARs from granule neurons abolished ketamine- and HNK-induced BDNF exocytosis in acute mouse hippocampal slices, establishing a presynaptic receptor mechanism for antidepressant-induced neurotrophin release. In CA3 pyramidal neurons that receive mossy fiber input, both compounds induced rapid remodeling of dendritic spines, resulting in increased spine density. Together, these findings identify presynaptic terminals as a previously unrecognized source of antidepressant-evoked BDNF release and establish a new cellular mechanism for the rapid synaptic effects of fast-acting antidepressants.

neuroscience↗

Sevoflurane inhibition of the developmentally expressed neuronal sodium channel Nav1.3

Neuronal voltage-gated sodium channels (Nav) are major targets for the neurophysiological actions of general anesthetics. In the adult brain, cell type-specific effects on synaptic transmission are attributed to the differential sensitivity to volatile anesthetics of specific Nav subtypes preferentially expressed in mature neurons (Nav1.1, Nav1.2, Nav1.6). Compared to mature neurons, neurons in the developing CNS are more excitable. Since the subtype-selective effects of volatile anesthetics on Nav during early development are unknown, we determined volatile anesthetic effects on Na+ currents mediated by Nav1.3, the principal Nav subtype expressed in developing neurons. Sevoflurane at clinically relevant concentrations inhibited peak Na+ current (INa) of human Nav1.3 heterologously expressed in HEK293T cells in a voltage- dependent manner, induced a -6.1 mV hyperpolarizing shift in the voltage dependence of steady- state inactivation, and slowed recovery from fast inactivation. Nav1.3-mediated Na+ currents also exhibited distinct activation properties associated with neuronal hyperexcitability, including prominent persistent currents and ramp currents, both of which were significantly reduced by sevoflurane. The major neuronal subtype Nav1.2 showed a more hyperpolarized voltage dependence of steady-state inactivation than Nav1.3. Consistent with its lower propensity for sustained repetitive firing, Nav1.2 exhibited minimal persistent and ramp currents, and these were unaffected by sevoflurane. These findings identify subtype-specific effects of the volatile anesthetic sevoflurane on neuronal Nav subtypes and suggest a mechanistic basis for increased anesthetic sensitivity in early neuronal differentiation and maturation.

pharmacology and toxicology↗

Functionally important binding site for a volatile anesthetic in a voltage-gated sodium channel identified by X-ray crystallography

Voltage-gated sodium channels (VGSCs), key mediators of excitability and synaptic transmission, are established and functionally relevant targets for volatile anaesthetic (VA) action. Using the structurally homologous prokaryotic VGSCs NavMs and NaChBac as models, we present a structure-function analysis of VGSC-VA interactions. We report that multiple VAs compete for binding sites on NavMs, and that these direct interactions mediate functional effects of sevoflurane on NavMs that mirror those attributed to VA effects in eukaryotic VGSCs, including human isoforms. Using X-ray crystallography, we determined the first atomic-resolution structure of a VA bound to a VGSC, showing sevoflurane displacing lipids to bind in an intramembranous hydrophobic pocket of NavMs. A conserved tyrosine residue within this binding site is critical for channel gating, and its substitution with alanine abolishes sevoflurane binding and selectively eliminates the characteristic anaesthetic-induced hyperpolarising shift of steady-state inactivation that reduces neuronal excitability at physiological membrane potentials. Finally, we provide evidence supporting VA action at the conserved sites in human VGSC isoforms. These findings define the first VA binding site in a VGSC. A membrane-mediated access pathway to the binding site leads to negative modulation of channel function that reduces neuronal activity and excitatory synaptic transmission in general anaesthesia.

biophysics↗

Nonspecific membrane bilayer perturbations by ivermectin underlie SARS-CoV-2 in vitro activity

Since it was proposed as a potential host-directed antiviral agent for SARS-CoV-2, the antiparasitic drug ivermectin has been investigated thoroughly in clinical trials, which have provided insufficient support for its clinical efficacy. To examine the potential for ivermectin to be repurposed as an antiviral agent, we therefore undertook a series of preclinical studies. Consistent with early reports, ivermectin decreased SARS-CoV-2 viral burden in in vitro models at low micromolar concentrations, five-to ten-fold higher than the reported toxic clinical concentration. At similar concentrations, ivermectin also decreased cell viability and increased biomarkers of cytotoxicity and apoptosis. Further mechanistic and profiling studies revealed that ivermectin nonspecifically perturbs membrane bilayers at the same concentrations where it decreases the SARS-CoV-2 viral burden, resulting in nonspecific modulation of membrane-based targets such as G-protein coupled receptors and ion channels. These results suggest that a primary molecular mechanism for the in vitro antiviral activity of ivermectin may be nonspecific membrane perturbation, indicating that ivermectin is unlikely to be translatable into a safe and effective antiviral agent. These results and experimental workflow provide a useful paradigm for performing preclinical studies on (pandemic-related) drug repurposing candidates. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=61 SRC="FIGDIR/small/563088v1_ufig1.gif" ALT="Figure 1"> View larger version (18K): org.highwire.dtl.DTLVardef@a21f94org.highwire.dtl.DTLVardef@1c76751org.highwire.dtl.DTLVardef@500930org.highwire.dtl.DTLVardef@8b6c05_HPS_FORMAT_FIGEXP M_FIG Graphical abstract C_FIG

pharmacology and toxicology↗