Overexpression of tau downregulated the mRNA levels of Kv channels and improved proliferation in N2A cells.

Microtubule binding protein tau has a crucial function in promoting the assembly and stabilization of microtubule. Besides tuning the action potentials, voltage-gated K+ channels (Kv) are important for cell proliferation and appear to play a role in the development of cancer. However, little is know...

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Main Authors: Xiantao Li, Ximu Hu, Xiaoqing Li, Xuran Hao
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4295873?pdf=render
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spelling doaj-fe6a52f6baba4a0485b2d9263dd35a112020-11-25T01:20:37ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01101e011662810.1371/journal.pone.0116628Overexpression of tau downregulated the mRNA levels of Kv channels and improved proliferation in N2A cells.Xiantao LiXimu HuXiaoqing LiXuran HaoMicrotubule binding protein tau has a crucial function in promoting the assembly and stabilization of microtubule. Besides tuning the action potentials, voltage-gated K+ channels (Kv) are important for cell proliferation and appear to play a role in the development of cancer. However, little is known about the possible interaction of tau with Kv channels in various tissues. In the present study, tau plasmids were transiently transfected into mouse neuroblastoma N2A cells to explore the possible linkages between tau and Kv channels. This treatment led to a downregulation of mRNA levels of several Kv channels, including Kv2.1, Kv3.1, Kv4.1, Kv9.2, and KCNH4, but no significant alteration was observed for Kv5.1 and KCNQ4. Furthermore, the macroscopic currents through Kv channels were reduced by 36.5% at +60 mV in tau-transfected N2A cells. The proliferation rates of N2A cells were also improved by the induction of tau expression and the incubation of TEA (tetraethylammonium) for 48 h by 120.9% and 149.3%, respectively. Following the cotransfection with tau in HEK293 cells, the mRNA levels and corresponding currents of Kv2.1 were significantly declined compared with single Kv2.1 transfection. Our data indicated that overexpression of tau declined the mRNA levels of Kv channels and related currents. The effects of tau overexpression on Kv channels provided an alternative explanation for low sensitivity to anti-cancer chemicals in some specific cancer tissues.http://europepmc.org/articles/PMC4295873?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Xiantao Li
Ximu Hu
Xiaoqing Li
Xuran Hao
spellingShingle Xiantao Li
Ximu Hu
Xiaoqing Li
Xuran Hao
Overexpression of tau downregulated the mRNA levels of Kv channels and improved proliferation in N2A cells.
PLoS ONE
author_facet Xiantao Li
Ximu Hu
Xiaoqing Li
Xuran Hao
author_sort Xiantao Li
title Overexpression of tau downregulated the mRNA levels of Kv channels and improved proliferation in N2A cells.
title_short Overexpression of tau downregulated the mRNA levels of Kv channels and improved proliferation in N2A cells.
title_full Overexpression of tau downregulated the mRNA levels of Kv channels and improved proliferation in N2A cells.
title_fullStr Overexpression of tau downregulated the mRNA levels of Kv channels and improved proliferation in N2A cells.
title_full_unstemmed Overexpression of tau downregulated the mRNA levels of Kv channels and improved proliferation in N2A cells.
title_sort overexpression of tau downregulated the mrna levels of kv channels and improved proliferation in n2a cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Microtubule binding protein tau has a crucial function in promoting the assembly and stabilization of microtubule. Besides tuning the action potentials, voltage-gated K+ channels (Kv) are important for cell proliferation and appear to play a role in the development of cancer. However, little is known about the possible interaction of tau with Kv channels in various tissues. In the present study, tau plasmids were transiently transfected into mouse neuroblastoma N2A cells to explore the possible linkages between tau and Kv channels. This treatment led to a downregulation of mRNA levels of several Kv channels, including Kv2.1, Kv3.1, Kv4.1, Kv9.2, and KCNH4, but no significant alteration was observed for Kv5.1 and KCNQ4. Furthermore, the macroscopic currents through Kv channels were reduced by 36.5% at +60 mV in tau-transfected N2A cells. The proliferation rates of N2A cells were also improved by the induction of tau expression and the incubation of TEA (tetraethylammonium) for 48 h by 120.9% and 149.3%, respectively. Following the cotransfection with tau in HEK293 cells, the mRNA levels and corresponding currents of Kv2.1 were significantly declined compared with single Kv2.1 transfection. Our data indicated that overexpression of tau declined the mRNA levels of Kv channels and related currents. The effects of tau overexpression on Kv channels provided an alternative explanation for low sensitivity to anti-cancer chemicals in some specific cancer tissues.
url http://europepmc.org/articles/PMC4295873?pdf=render
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AT xiaoqingli overexpressionoftaudownregulatedthemrnalevelsofkvchannelsandimprovedproliferationinn2acells
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