Ion channel compartments in photoreceptors: evidence from salamander rods with intact and ablated terminals.
نویسندگان
چکیده
Vertebrate photoreceptors are highly polarized sensory cells in which several different ionic currents have been characterized. In the present study we used whole cell voltage-clamp and optical imaging techniques, the former combined with microsurgical manipulations, and simultaneous recording of membrane current and intracellular calcium signals to investigate the spatial distribution of ion channels within isolated salamander rods. In recordings from intact rods with visible terminals, evidence for five previously identified ionic currents was obtained. These include two Ca(2+)-dependent, i.e., a Ca(2+)-dependent chloride current [I(Cl(Ca))] and a large-conductance Ca(2+)- and voltage-dependent K(+) or BK current [I(K(Ca))], and three voltage-dependent currents, i.e., a delayed-rectifier type current [I(K(V))], a hyperpolarization-activated cation current (I(h)), and a dihydropyridine-sensitive L-type calcium current (I(Ca)). Of these, I(Cl(Ca)) was highly correlated with the presence of a terminal; rods with visible terminals expressed I(Cl(Ca)) without exception (n = 125), whereas approximately 71% of rods (40/56) without visible terminals lacked I(Cl(Ca)). More significantly, I(Cl(Ca)) was absent from all rods (n = 33) that had their terminals ablated, and recordings from the same cell before and after terminal ablation led, in all cases (n =10), to the loss of I(Cl(Ca)). In contrast, I(K(Ca)), I(K(V)), and I(h) remained largely intact after terminal ablation, suggesting that they arose principally from ion channels located in the soma and/or inner segment. The outward I(K)((Ca)) in terminal-ablated rods was reversibly suppressed on "puffing" a Ca(2+)-free extracellular solution over the soma and was appreciably enhanced by the L-type Ca(2+) channel agonist, Bay K 8644 (0.1-2 microM). These data indicate that rod photoreceptors possess discrete targeting mechanisms that preferentially sort ion channels mediating I(Cl(Ca)) to the terminal.
منابع مشابه
Imaging of Ca2+ dynamics within the presynaptic terminals of salamander rod photoreceptors.
Although the overall importance of Ca(2+) as a mediator of cell signaling and neurotransmitter release has long been appreciated, the details of Ca(2+) dynamics within the inner segments of vertebrate rod photoreceptors are just beginning to be elucidated. Even less is known regarding Ca(2+) dynamics within the rod presynaptic terminal compartment. Using fura-2 to report changes in intracellula...
متن کاملImaging of Ca Dynamics Within the Presynaptic Terminals of Salamander Rod Photoreceptors
Steele, Ernest C., Jr., Xiaoming Chen, P. Michael Iuvone, and Peter R. MacLeish. Imaging of Ca dynamics within the presynaptic terminals of salamander rod photoreceptors. J Neurophysiol 94: 4544–4553, 2005. First published August 17, 2005; doi:10.1152/jn.01193.2004. Although the overall importance of Ca as a mediator of cell signaling and neurotransmitter release has long been appreciated, the ...
متن کاملCannabinoid receptor activation differentially modulates ion channels in photoreceptors of the tiger salamander.
Cannabinoid CB1 receptors have been detected in retinas of numerous species, with prominent labeling in photoreceptor terminals of the chick and monkey. CB1 labeling is well-conserved across species, suggesting that CB1 receptors might also be present in photoreceptors of the tiger salamander. Synaptic transmission in vertebrate photoreceptors is mediated by L-type calcium currents-currents tha...
متن کاملIn Intact Cone Photoreceptors, a Ca2+-dependent, Diffusible Factor Modulates the cGMP-gated Ion Channels Differently than in Rods
We investigated the modulation of cGMP-gated ion channels in single cone photoreceptors isolated from a fish retina. A new method allowed us to record currents from an intact outer segment while controlling its cytoplasmic composition by superfusion of the electropermeabilized inner segment. The sensitivity of the channels to agonists in the intact outer segment differs from that measured in me...
متن کاملWeak endogenous Ca2+ buffering supports sustained synaptic transmission by distinct mechanisms in rod and cone photoreceptors in salamander retina
Differences in synaptic transmission between rod and cone photoreceptors contribute to different response kinetics in rod- versus cone-dominated visual pathways. We examined Ca(2+) dynamics in synaptic terminals of tiger salamander photoreceptors under conditions that mimicked endogenous buffering to determine the influence on kinetically and mechanistically distinct components of synaptic tran...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Journal of neurophysiology
دوره 98 1 شماره
صفحات -
تاریخ انتشار 2007