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Volume 270, Number 38, Issue of September 22, pp. 22406-22411, 1995
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
Identification of Kv1.1 Expression by Murine CD4CD8 Thymocytes
A ROLE FOR VOLTAGE-DEPENDENT K CHANNELS IN MURINE THYMOCYTE DEVELOPMENT

(Received for publication, April 17, 1995; and in revised form, June 20, 1995)

Bruce D. Freedman ,&nbsp;<WBR> Bernd K. Fleischmann ,&nbsp;<WBR> Jennifer A. Punt ,&nbsp;<WBR> Glen Gaulton ,&nbsp;<WBR> Yasuhiro Hashimoto ,&nbsp;<WBR> Michael I. Kotlikoff

The patch-clamp recording technique and RNApolymerase chain reaction were used to identify the voltage-dependent K channels expressed by murine fetal and adult CD4CD8 thymocytes. Two distinct currents, encoded by the genes Kv1.1 and Kv1.3 were identified based upon their biophysical and pharmacologic characteristics and confirmed with RNA-polymerase chain reaction. Peptide blockers of Kv1.1 and Kv1.3 gene products were also applied to a murine fetal thymic organ culture system to investigate the developmental role of these K channels. Dendrotoxin (DTX) and charybdotoxin (CTX), antagonists of Kv1.1 and Kv1.3 channels, respectively, decreased thymocyte yields in organ culture without affecting thymocyte viability. DTX-treated thymi contained 56 ± 8% (n = 8 experiments), and CTX-treated thymi contained 74 ± 4% (n = 7 experiments) as many thymocytes as untreated lobes. DTX and CTX also altered the developmental progression of thymocytes in fetal organ culture. These data provide the first evidence of Kv1.1 expression in a lymphoid cell and indicate that thymocyte voltage-dependent K channels are critical to thymocyte preclonal expansion and/or maturation.




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