ABSTRACT
As an essential trace element, copper can be toxic in mammalian cells when present in excess. Metallothioneins (MTs) are small, cysteine-rich proteins that avidly bind copper and thus play an important role in detoxification. Yeast CUP1 is a member of the MT gene family. The aim of this study was to determine whether yeast CUP1 could bind copper effectively and protect cells against copper stress. In this study, CUP1 expression was determined by quantitative real-time PCR, and copper content was detected by inductively coupled plasma mass spectrometry. Production of intracellular reactive oxygen species (ROS) was evaluated using the 2',7'-dichlorofluorescein-diacetate (DCFH-DA) assay. Cellular viability was detected using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, and the cell cycle distribution of CUP1 was analyzed by fluorescence-activated cell sorting. The data indicated that overexpression of yeast CUP1 in HeLa cells played a protective role against copper-induced stress, leading to increased cellular viability (P<0.05) and decreased ROS production (P<0.05). It was also observed that overexpression of yeast CUP1 reduced the percentage of G1 cells and increased the percentage of S cells, which suggested that it contributed to cell viability. We found that overexpression of yeast CUP1 protected HeLa cells against copper stress. These results offer useful data to elucidate the mechanism of the MT gene on copper metabolism in mammalian cells.
Subject(s)
Animals , Humans , Mammals/physiology , Pheromones/physiology , Behavior, Animal/physiology , Behavior/physiology , Odorants , Olfactory Bulb/physiology , Olfactory Mucosa/physiology , Olfactory Pathways/anatomy & histology , Olfactory Pathways/physiology , Olfactory Receptor Neurons/physiology , Pheromones, Human/physiology , Smell/physiologyABSTRACT
The rodent preputial gland is one of the major sources of odours and is reported to be involved in several behavioural activities. However, how the preputial gland initiates the olfactory response to manifest the effects is not known. Olfactory receptor neurons (ORNs) present in the olfactory epithelium are involved in the perception of odorant/pheromonal compounds. In the present study, the response of rat ORNs to preputial gland extract was evaluated by calcium imaging analysis. We found that some rat ORNs responded to the preputial gland extract by exhibiting an intracellular calcium response. By contrast, the ORNs did not respond at all to the foot pad extract (control). The results indicated that the substances contained in the preputial gland might interact with a type of receptor expressed in the female rat ORNs, suggested to manifest the behavioural responses, such as social and sexual interactions. This study provided the first evidence of activation of ORNs by the preputial gland extract.
Subject(s)
Action Potentials/physiology , Animals , Calcium Signaling/physiology , Exocrine Glands/physiology , Female , Male , Microscopy, Confocal/methods , Olfactory Receptor Neurons/cytology , Olfactory Receptor Neurons/physiology , Rats , Rats, Wistar , Voltage-Sensitive Dye Imaging/methodsABSTRACT
Based on indirect evidence, a role for synaptically released copper and zinc as modulators of neuronal activity has been proposed. To test this proposal directly, we studied the effect of copper, zinc, and other divalent cations on voltage-dependent currents in dissociated toad olfactory neurons and on their firing rate induced by small depolarizing currents. Divalent cations in the nanomolar range sped up the activation kinetics and increased the amplitude of the inward sodium current. In the micromolar range, they caused a dose dependent inhibition of the inward Na+ and Ca2+ currents (INa and ICa) and reduced de amplitude of the Ca2+-dependent K+ outward current (ICa-K). On the other hand, the firing rate of olfactory neurons increased when exposed to nanomolar concentration of divalent cations and decreased when exposed to micromolar concentrations. This biphasic effect of divalent cations on neuronal excitability may be explained by the interaction of these ions with high and low affinity sites in voltage-gated channels. Our results support the idea that these ions are normal modulators of neuronal excitability.
Subject(s)
Animals , Copper/pharmacology , Olfactory Receptor Neurons/drug effects , Zinc/pharmacology , Anura , Action Potentials/drug effects , Action Potentials/physiology , Cell Membrane , Cations, Divalent/pharmacology , Electric Stimulation , Membrane Potentials/drug effects , Membrane Potentials/physiology , Olfactory Receptor Neurons/physiology , Signal Transduction/physiologyABSTRACT
Odorant detection takes place at the receptor neurons of the olfactory epithelium and odorant discrimination relies in an important degree on these chemosensory cells. Here we review the evidence for the participation of multiple transduction pathways in the mechanisms of odor recognition in olfactory neurons