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Synaptic localisation of SRF coactivators, MKL1 and MKL2, and their role in dendritic spine morphology

The megakaryoblastic leukaemia (MKL) family are serum response factor (SRF) coactivators, which are highly expressed in the brain. Accordingly, MKL plays important roles in dendritic morphology, neuronal migration, and brain development. Further, nucleotide substitutions in the MKL1 and MKL2 genes a...

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Autores principales: Kaneda, Marisa, Sakagami, Hiroyuki, Hida, Yamato, Ohtsuka, Toshihisa, Satou, Natsumi, Ishibashi, Yuta, Fukuchi, Mamoru, Krysiak, Anna, Ishikawa, Mitsuru, Ihara, Daisuke, Kalita, Katarzyna, Tabuchi, Akiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768758/
https://www.ncbi.nlm.nih.gov/pubmed/29335431
http://dx.doi.org/10.1038/s41598-017-18905-7
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author Kaneda, Marisa
Sakagami, Hiroyuki
Hida, Yamato
Ohtsuka, Toshihisa
Satou, Natsumi
Ishibashi, Yuta
Fukuchi, Mamoru
Krysiak, Anna
Ishikawa, Mitsuru
Ihara, Daisuke
Kalita, Katarzyna
Tabuchi, Akiko
author_facet Kaneda, Marisa
Sakagami, Hiroyuki
Hida, Yamato
Ohtsuka, Toshihisa
Satou, Natsumi
Ishibashi, Yuta
Fukuchi, Mamoru
Krysiak, Anna
Ishikawa, Mitsuru
Ihara, Daisuke
Kalita, Katarzyna
Tabuchi, Akiko
author_sort Kaneda, Marisa
collection PubMed
description The megakaryoblastic leukaemia (MKL) family are serum response factor (SRF) coactivators, which are highly expressed in the brain. Accordingly, MKL plays important roles in dendritic morphology, neuronal migration, and brain development. Further, nucleotide substitutions in the MKL1 and MKL2 genes are found in patients with schizophrenia and autism spectrum disorder, respectively. Thus, studies on the precise synaptic localisation and function of MKL in neurons are warranted. In this study, we generated and tested new antibodies that specifically recognise endogenously expressed MKL1 and MKL2 proteins in neurons. Using these reagents, we biochemically and immunocytochemically show that MKL1 and MKL2 are localised at synapses. Furthermore, shRNA experiments revealed that postsynaptic deletion of MKL1 or MKL2 reduced the percentage of mushroom- or stubby-type spines in cultured neurons. Taken together, our findings suggest that MKL1 and MKL2 are present at synapses and involved in dendritic spine maturation. This study may, at least in part, contribute to better understanding of the molecular mechanisms underlying MKL-mediated synaptic plasticity and neurological disorders.
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spelling pubmed-57687582018-01-25 Synaptic localisation of SRF coactivators, MKL1 and MKL2, and their role in dendritic spine morphology Kaneda, Marisa Sakagami, Hiroyuki Hida, Yamato Ohtsuka, Toshihisa Satou, Natsumi Ishibashi, Yuta Fukuchi, Mamoru Krysiak, Anna Ishikawa, Mitsuru Ihara, Daisuke Kalita, Katarzyna Tabuchi, Akiko Sci Rep Article The megakaryoblastic leukaemia (MKL) family are serum response factor (SRF) coactivators, which are highly expressed in the brain. Accordingly, MKL plays important roles in dendritic morphology, neuronal migration, and brain development. Further, nucleotide substitutions in the MKL1 and MKL2 genes are found in patients with schizophrenia and autism spectrum disorder, respectively. Thus, studies on the precise synaptic localisation and function of MKL in neurons are warranted. In this study, we generated and tested new antibodies that specifically recognise endogenously expressed MKL1 and MKL2 proteins in neurons. Using these reagents, we biochemically and immunocytochemically show that MKL1 and MKL2 are localised at synapses. Furthermore, shRNA experiments revealed that postsynaptic deletion of MKL1 or MKL2 reduced the percentage of mushroom- or stubby-type spines in cultured neurons. Taken together, our findings suggest that MKL1 and MKL2 are present at synapses and involved in dendritic spine maturation. This study may, at least in part, contribute to better understanding of the molecular mechanisms underlying MKL-mediated synaptic plasticity and neurological disorders. Nature Publishing Group UK 2018-01-15 /pmc/articles/PMC5768758/ /pubmed/29335431 http://dx.doi.org/10.1038/s41598-017-18905-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kaneda, Marisa
Sakagami, Hiroyuki
Hida, Yamato
Ohtsuka, Toshihisa
Satou, Natsumi
Ishibashi, Yuta
Fukuchi, Mamoru
Krysiak, Anna
Ishikawa, Mitsuru
Ihara, Daisuke
Kalita, Katarzyna
Tabuchi, Akiko
Synaptic localisation of SRF coactivators, MKL1 and MKL2, and their role in dendritic spine morphology
title Synaptic localisation of SRF coactivators, MKL1 and MKL2, and their role in dendritic spine morphology
title_full Synaptic localisation of SRF coactivators, MKL1 and MKL2, and their role in dendritic spine morphology
title_fullStr Synaptic localisation of SRF coactivators, MKL1 and MKL2, and their role in dendritic spine morphology
title_full_unstemmed Synaptic localisation of SRF coactivators, MKL1 and MKL2, and their role in dendritic spine morphology
title_short Synaptic localisation of SRF coactivators, MKL1 and MKL2, and their role in dendritic spine morphology
title_sort synaptic localisation of srf coactivators, mkl1 and mkl2, and their role in dendritic spine morphology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768758/
https://www.ncbi.nlm.nih.gov/pubmed/29335431
http://dx.doi.org/10.1038/s41598-017-18905-7
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