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Cells ; 10(4)2021 03 24.
Article in English | MEDLINE | ID: mdl-33805168

ABSTRACT

The growth factor TGFß and the mechanosensitive calcium-permeable cation channel TRPV4 are both important for the development and maintenance of many tissues. Although TRPV4 and TGFß both affect core cellular functions, how their signals are integrated is unknown. Here we show that pharmacological activation of TRPV4 significantly increased the canonical response to TGFß stimulation in chondrocytes. Critically, this increase was only observed when TRPV4 was activated after, but not before TGFß stimulation. The increase was prevented by pharmacological TRPV4 inhibition or knockdown and is calcium/CamKII dependent. RNA-seq analysis after TRPV4 activation showed enrichment for the TGFß signalling pathway and identified JUN and SP1 as key transcription factors involved in this response. TRPV4 modulation of TGFß signalling represents an important pathway linking mechanical signalling to tissue development and homeostasis.


Subject(s)
Chondrocytes/metabolism , Signal Transduction , TRPV Cation Channels/metabolism , Transforming Growth Factor beta/metabolism , Animals , Calcium/metabolism , Calmodulin/metabolism , Cattle , Chondrocytes/drug effects , Gene Expression Regulation/drug effects , Genes, Reporter , Humans , Leucine/analogs & derivatives , Leucine/pharmacology , Mice , Proto-Oncogene Proteins c-jun/metabolism , RNA-Seq , Signal Transduction/drug effects , Signal Transduction/genetics , Sp1 Transcription Factor/metabolism , Sulfonamides/pharmacology , Time Factors
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