TABLE OF CONTENTS |
March 2016 Volume 18, Issue 3 |
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 | Editorial Commentary Reviews News and Views Articles Letters Resource Corrigenda Erratum
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The Geoffrey Beene Cancer Research Center at Memorial Sloan Kettering Cancer Center, Nature, Nature Cell Biology and Nature Reviews Cancer present: CANCER AS AN EVOLVING AND SYSTEMIC DISEASE March 12-15, 2016 | New York, NY, USA REGISTER NOW! |  | | |
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Editorial | Top |
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Stem cells in the limelight p235 doi:10.1038/ncb3315 Stem cell biology has emerged as one of the most exciting areas of basic and biomedical research. This month, we launch a series of specially commissioned articles that discuss recent advances and challenges in this field.
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Commentary | Top |
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Raising the standards of stem cell line quality pp236 - 237 Michael P. Yaffe, Scott A. Noggle and Susan L. Solomon doi:10.1038/ncb3313 Yaffe and colleagues discuss the issues surrounding the authentication and quality of induced pluripotent stem cells.
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Reviews | Top |
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Stem cells versus plasticity in liver and pancreas regeneration pp238 - 245 Janel L. Kopp, Markus Grompe and Maike Sander doi:10.1038/ncb3309 Sander and colleagues discuss recent evidence for and against the roles of stem cells versus the plasticity of mature cell types in response to injury during regeneration of the adult liver and pancreas.
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Organoids as an in vitro model of human development and disease pp246 - 254 Aliya Fatehullah, Si Hui Tan and Nick Barker doi:10.1038/ncb3312 Barker and colleagues review the history and recent developments of organoid cultures derived from pluripotent stem cells and adult epithelia, and discuss how the technology can be used for basic research as well as translational applications.
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News and Views | Top |
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Roles for mesenchymal stem cells as medicinal signaling cells Understanding the in vivo identity and function of mesenchymal stem cells (MSCs) is vital to fully exploit their therapeutic potential. This poster summarizes current thinking regarding the role of MSCs in vivo and also describes how to isolate MSCs and grow them in vitro. Download the poster free online.
Produced with support from: STEMCELL Technologies | | | |
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Articles | Top |
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Modular activation of Rho1 by GPCR signalling imparts polarized myosin II activation during morphogenesis pp261 - 270 Stephen Kerridge, Akankshi Munjal, Jean-Marc Philippe, Ankita Jha, Alain Garcia de las Bayonas et al. doi:10.1038/ncb3302 Lecuit and colleagues show that, depending on its interaction partner, the G-protein-coupled receptor Smog regulates myosin II activation in different locations during Drosophila morphogenesis.
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EXD2 promotes homologous recombination by facilitating DNA end resection pp271 - 280 Ronan Broderick, Jadwiga Nieminuszczy, Hannah T. Baddock, Rajashree A. Deshpande, Opher Gileadi et al. doi:10.1038/ncb3303 DNA resection is the first step of double-strand break repair by homologous recombination. Broderick et al. find that EXD2 plays a key role in this process by acting as an essential cofactor for the MRN complex.
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DNA damage signalling targets the kinetochore to promote chromatin mobility pp281 - 290 Jonathan Strecker, Gagan D. Gupta, Wei Zhang, Mikhail Bashkurov, Marie-Claude Landry et al. doi:10.1038/ncb3308 Durocher and colleagues find that in budding yeast, the movement of chromosomes induced by DNA breaks is due to the loss of attachment of kinetochores to spindle pole bodies and of telomeres to the nuclear periphery, and may promote checkpoint arrest.
See also: News and Views by Nakajima & Haber |
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CHIP controls necroptosis through ubiquitylation- and lysosome-dependent degradation of RIPK3 pp291 - 302 Jinho Seo, Eun-Woo Lee, Hyerim Sung, Daehyeon Seong, Yves Dondelinger et al. doi:10.1038/ncb3314 Receptor-interacting protein kinase 3 (RIPK3) is a key regulator of necroptosis. Seo et al. show that the E3 ligase CHIP mediates ubiquitylation and lysosomal degradation of RIPK3, thus regulating both necrosome formation and necroptosis.
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Two NO COST pilot projects to be awarded. Register for our webcast on Building Better Therapeutics with Metabolomics and be eligible to submit your abstract for 1 of 2 50 sample projects using metabolomics. Register for the webcast free online. | | | |
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Letters | Top |
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β-Arrestin drives MAP kinase signalling from clathrin-coated structures after GPCR dissociation pp303 - 310 K. Eichel, D. Jullié and M. von Zastrow doi:10.1038/ncb3307 Eichel et al. show that β-arrestin-mediated MAPK activation by GPCRs involves dissociation of β-arrestin from its activating GPCR, and accumulation of β-arrestin in clathrin-coated structures, where it promotes MAPK signalling.
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Extracellular matrix scaffolding guides lumen elongation by inducing anisotropic intercellular mechanical tension pp311 - 318 Qiushi Li, Yue Zhang, Perrine Pluchon, Jeffrey Robens, Keira Herr et al. doi:10.1038/ncb3310 By culturing rat hepatocyte doublets in microwells with controlled ECM environments, Viasnoff and colleagues show that the lumen between the cells extends anisotropically towards regions of lower intercellular tension.
See also: News and Views by Wee & Yap |
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Secreted IGFBP5 mediates mTORC1-dependent feedback inhibition of IGF-1 signalling pp319 - 327 Ming Ding, Richard K. Bruick and Yonghao Yu doi:10.1038/ncb3311 By proteomics analysis of conditioned media from cells with constitutive mTORC1 activity, Yu and colleagues identify IGF binding protein 5 (IGFBP5) as a protein that is induced by mTORC1 through HIF1 and that blocks IGF-1 signalling.
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Dicer1–miR-328–Bace1 signalling controls brown adipose tissue differentiation and function pp328 - 336 Matteo Oliverio, Elena Schmidt, Jan Mauer, Catherina Baitzel, Nils Hansmeier et al. doi:10.1038/ncb3316 Kornfeld and colleagues identify miRNAs that are dysregulated in brown adipose tissue in mouse models of obesity and ageing, and show that miR-328 targets Bace1 to promote brown adipogenesis.
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Resource | Top |
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A combined binary interaction and phenotypic map of C. elegans cell polarity proteins pp337 - 346 Thijs Koorman, Diana Klompstra, Monique van der Voet, Irma Lemmens, João J. Ramalho et al. doi:10.1038/ncb3300 Boxem and colleagues perform a yeast two-hybrid screen to identify interactions between C. elegans polarity genes, followed by an RNAi screen to identify the functions of interaction pairs in the establishment and maintenance of cell polarity in various tissues.
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Corrigenda | Top |
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Corrigendum: Independent and coordinate trafficking of single Drosophila germ plasm mRNAs p347 Shawn C. Little, Kristina S. Sinsimer, Jack J. Lee, Eric F. Wieschaus and Elizabeth R. Gavis doi:10.1038/ncb3317
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Corrigendum: Systematic proteomics of the VCP–UBXD adaptor network identifies a role for UBXN10 in regulating ciliogenesis p347 Malavika Raman, Mikhail Sergeev, Maija Garnaas, John R. Lydeard, Edward L. Huttlin et al. doi:10.1038/ncb3318
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Erratum | Top |
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Erratum: Actin puts the squeeze on Drosophila glue secretion p347 Christien J. Merrifield doi:10.1038/ncb3322
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