Kilpatrick Bethan S, Yates Elizabeth, Grimm Christian, Schapira Anthony H, Patel Sandip
Department of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK.
Center for Integrated Protein Science CIPSM and Department of Pharmacy - Center for Drug Research, Ludwig-Maximilians-Universität München, München 81377, Germany.
J Cell Sci. 2016 Oct 15;129(20):3859-3867. doi: 10.1242/jcs.190322. Epub 2016 Aug 30.
Transient receptor potential (TRP) mucolipins (TRPMLs), encoded by the MCOLN genes, are patho-physiologically relevant endo-lysosomal ion channels crucial for membrane trafficking. Several lines of evidence suggest that TRPMLs mediate localised Ca release but their role in Ca signalling is not clear. Here, we show that activation of endogenous and recombinant TRPMLs with synthetic agonists evoked global Ca signals in human cells. These signals were blocked by a dominant-negative TRPML1 construct and a TRPML antagonist. We further show that, despite a predominant lysosomal localisation, TRPML1 supports both Ca release and Ca entry. Ca release required lysosomal and ER Ca stores suggesting that TRPMLs, like other endo-lysosomal Ca channels, are capable of 'chatter' with ER Ca channels. Our data identify new modalities for TRPML1 action.
瞬时受体电位(TRP)黏脂素(TRPMLs)由MCOLN基因编码,是病理生理学相关的内溶酶体离子通道,对膜运输至关重要。多项证据表明,TRPMLs介导局部钙释放,但其在钙信号传导中的作用尚不清楚。在此,我们表明,用合成激动剂激活内源性和重组TRPMLs会在人类细胞中引发全局钙信号。这些信号被显性负性TRPML1构建体和TRPML拮抗剂阻断。我们进一步表明,尽管TRPML1主要定位于溶酶体,但它支持钙释放和钙内流。钙释放需要溶酶体和内质网钙库,这表明TRPMLs与其他内溶酶体钙通道一样,能够与内质网钙通道“交流”。我们的数据确定了TRPML1作用的新模式。