DIFFERENTIAL EXPRESSION OF HYPERPOLARIZATION-ACTIVATED CURRENTS REVEALS DISTINCT CLASSES OF VISUAL CORTICAL PROJECTION NEURONS

Citation
Js. Solomon et al., DIFFERENTIAL EXPRESSION OF HYPERPOLARIZATION-ACTIVATED CURRENTS REVEALS DISTINCT CLASSES OF VISUAL CORTICAL PROJECTION NEURONS, The Journal of neuroscience, 13(12), 1993, pp. 5082-5091
Citations number
27
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
02706474
Volume
13
Issue
12
Year of publication
1993
Pages
5082 - 5091
Database
ISI
SICI code
0270-6474(1993)13:12<5082:DEOHCR>2.0.ZU;2-D
Abstract
Combining in vivo retrograde labeling and in vitro electrophysiologica l recording techniques, we examined the distributions, densities, and biophysical properties of hyperpolarization-activated inward currents in two types of isolated, identified visual cortical projection neuron s, superior colliculus-projecting (SCP) and callosal-projecting (CP) c ells. In SCP cells, two kinetically distinct time-dependent hyperpolar ization-activated inward current components are present. We have terme d these I(h,f) and I(h,s) to denote the fast and slow components, resp ectively, of I(h) activation. In CP cells, in contrast, I(h,f) and I(h ,s) are differentially expressed. In 59% of the CP cells examined, for example, both I(h,f) and I(h,s) were present. The properties of the c urrents are indistinguishable from those recorded from SCP cells, alth ough both I(h,f) and I(h,s) are expressed at significantly lower densi ties in this subset of CP cells (as compared to the current densities in SCP cells). Of the remaining 41% of the CP cells studied, 26% were found to express only I(h,s), and 12% of the cells expressed neither I (h,f) nor I(h,s). Taken together, these results reveal that the electr ical properties of CP visual cortical neurons are considerably more he terogeneous than those of SCP cells. The differential expression of I( h,f) and I(h,s) is expected to influence the integrated responses of d ifferent types of cortical projection neurons to excitatory and inhibi tory synaptic inputs.