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- How cell and tissue humanized mice are generated
- The application of humanized models in basic and applied research
- And, read an evaluation of the available super immunodeficient models for cell and tissue
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TABLE OF CONTENTS
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December 2014 Volume 15, Issue 12 |
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 | Obituary Commentary News and Views Research Highlights Review Articles Resource | |
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Obituary | Top |
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Ray D. Owen 1915-2014 p1091 Michael P Cancro doi:10.1038/ni.3033 |
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Commentary | Top |
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The physician scientist: balancing clinical and research duties pp1092 - 1094 Penelope A Morel and Gillian Ross doi:10.1038/ni.3010 Physician scientists bridge the gap between biomedical research and clinical practice. However, the continuing decrease in number of people who choose this career path poses a threat to the advancement of biomedical science and the translation of research findings to clinical practice. |
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News and Views | Top |
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Research Highlights | Top |
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Fatty acid regulation of TH17 cells | IL-37 as an adaptive dampener | Computational toolbox | Neurotrophic receptors in HSCs | TH1 identity | Inflammation super-enhancers |
Review | Top |
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Molecular regulation of effector and memory T cell differentiation pp1104 - 1115 John T Chang, E John Wherry and Ananda W Goldrath doi:10.1038/ni.3031 |
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Articles | Top |
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Chitinase-like proteins promote IL-17-mediated neutrophilia in a tradeoff between nematode killing and host damage pp1116 - 1125 Tara E Sutherland, Nicola Logan, Dominik Ruckerl, Alison A Humbles, Stuart M Allan et al. doi:10.1038/ni.3023 Type 2 immune responses are often associated with the expression of chitinase-like Ym proteins, but their role is unclear. Allen and colleagues show that Ym1 and Ym2 act on γδ T cells to increase their expression of IL-17A and enhance the recruitment of neutrophils.
See also: News and Views by Muallem & Hunter |
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RNA viruses promote activation of the NLRP3 inflammasome through a RIP1-RIP3-DRP1 signaling pathway pp1126 - 1133 Xiaqiong Wang, Wei Jiang, Yiqing Yan, Tao Gong, Jiahuai Han et al. doi:10.1038/ni.3015 The mechanisms by which viruses activate the NLRP3 inflammasome remain unclear. Zhou and colleagues show that RNA viruses initiate a RIP1-RIP3 complex that drives mitochondrial damage and activation of the NLRP3 inflammasome independently of necrosis.
See also: News and Views by Rayamajhi & Miao |
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A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4 pp1134 - 1142 Laia Alsina, Elisabeth Israelsson, Matthew C Altman, Kristen K Dang, Pegah Ghandil et al. doi:10.1038/ni.3028 People with loss of function of MyD88 or IRAK4 have a surprisingly limited altered phenotype. Chaussabel and colleagues use a systems approach to identify defined signaling modules that are altered in such people.
See also: News and Views by Tough |
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A central role for Notch in effector CD8+ T cell differentiation pp1143 - 1151 Ronald A Backer, Christina Helbig, Rebecca Gentek, Andrew Kent, Brian J Laidlaw et al. doi:10.1038/ni.3027 Activated CD8+ T cells must 'choose' between the terminal effector cell fate or the memory precursor cell fate. Amsen and colleagues find that the cell surface receptor Notch controls this 'choice'. |
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Autophagy is essential for effector CD8+ T cell survival and memory formation pp1152 - 1161 Xiaojin Xu, Koichi Araki, Shuzhao Li, Jin-Hwan Han, Lilin Ye et al. doi:10.1038/ni.3025 Autophagy has essential roles in cellular energy mobilization and homeostasis, but its role in T cell memory formation is remains poorly understood. Ahmed and colleagues demonstrate that autophagy is critical for the survival of cytotoxic memory cells. |
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A microRNA upregulated in asthma airway T cells promotes TH2 cytokine production pp1162 - 1170 Laura J Simpson, Sana Patel, Nirav R Bhakta, David F Choy, Hans D Brightbill et al. doi:10.1038/ni.3026 miRNAs 'tune' gene expression to orchestrate cell activity. Ansel and colleagues show that miR-19 modulates TH2 cytokine production by targeting TH2-specific as well as general T cell-activation pathways. |
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The transcription repressors Bach2 and Bach1 promote B cell development by repressing the myeloid program pp1171 - 1180 Ari Itoh-Nakadai, Reina Hikota, Akihiko Muto, Kohei Kometani, Miki Watanabe-Matsui et al. doi:10.1038/ni.3024 The role of the repressors Bach1 and Bach2 in early B cell development is unclear. Igarashi and colleagues have now found these Bach factors directly repress various myeloid genes in common lymphoid progenitors to restrict a B cell lineage fate. |
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Resource | Top |
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High-dimensional analysis of the murine myeloid cell system pp1181 - 1189 Burkhard Becher, Andreas Schlitzer, Jinmiao Chen, Florian Mair, Hermi R Sumatoh et al. doi:10.1038/ni.3006 Myeloid cells show great phenotypic and functional diversity. Newell and colleagues use mass cytometry with a panel of 38 mouse myeloid markers to describe myeloid cell phenotypic diversity in unprecedented depth within eight different tissues.
See also: News and Views by Irish |
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