Tuesday, February 17, 2015

Nature Immunology Contents: March 2015 Volume 16 pp 215 - 326

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TABLE OF CONTENTS

March 2015 Volume 16, Issue 3

Commentary
News and Views
Research Highlights
Review
Articles
Resources
Corrigenda
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  • The utilization of spontaneous immune deficient mice
  • GEM model application in Oncology research
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Nature Insight Frontiers in biology

This year's Frontiers in Biology Insight covers the amygdala and how technology is helping us to understand its complex connectivity, innate lymphoid cells, nutrient-sensing mechanisms in mammals, a form of cell death called necroptosis, and the regulation and function of DNA methylation and its use as a cellular marker. 

Access the Insight online.
 
 

Commentary

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Feeding immunity: skepticism, delicacies and delights   pp215 - 219
Marc Veldhoen and Henrique Veiga-Fernandes
doi:10.1038/ni.3100
There are clear epidemiological links between nutrition and immunological function, but a dearth of mechanistic insights has made this topic controversial. Veldhoen and Veiga-Fernandes discuss this controversy and explore ways to take this research forward.

News and Views

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LincRNA signatures in human lymphocytes   pp220 - 222
Benoit T Roux and Mark A Lindsay
doi:10.1038/ni.3106
Sequencing studies have provided a comprehensive catalog of the expression of intergenic long noncoding RNAs (lincRNAs) in 13 subsets of human T cells and B cells. Subtype-selective lincRNAs are among those identified, including linc-MAF-4, that might regulate T cell differentiation.

See also: Resource by Ranzani et al.

Profiling the diversity of innate lymphoid cells   pp222 - 224
Andreas Diefenbach
doi:10.1038/ni.3107
Genome-wide transcriptional profiling of tissue-resident innate lymphoid cells (ILCs) has provided important insight not only into their developmental relationships and phenotypic plasticity but also into previously unknown functions.

See also: Resource by Robinette et al.

It takes CK2 to suppress TH2   pp224 - 225
Deepali V Sawant and Alexander L Dent
doi:10.1038/ni.3104
Optimal immunosuppression by regulatory T cells (Treg cells) relies on gene-expression and signaling modules that are customized to the target cell. The kinase CK2 is upregulated in Treg cells and controls a newly identified Treg cell subset that acts on dendritic cells to suppress T helper type 2 inflammatory responses in the lungs.

See also: Article by Ulges et al.

IL-1 watches the watchmen   pp226 - 227
Alejandro V Villarino and Arian Laurence
doi:10.1038/ni.3105
Direct antagonism between interleukin1 (IL-1) and the vitamin A metabolite retinoic acid tips the balance between differentiation into the TH17 subset of helper T cells or into regulatory T cells by influencing the transcription factors STAT3 and STAT5.

See also: Article by Basu et al.

Immunology
JOBS of the week
Postdoctoral Fellow in Cellular Immunology
University of Crete, Medical School
Postdoctoral Researcher in Immunology
United Arab Emiraes University
Postdoctoral Position in Cancer Immunology
Universität Basel
Faculty, Immunology Research / Immunotherapy
University of Virginia
Open Rank Faculty Position
University of North Carolina at Chapel Hill
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Nutritional Immunology: Role in Health and Disease
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Research Highlights

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Profiling carbohydrate recognition | Dopamine controls NLRP3 | Healing the CNS | Immunological complementation | Venom activity | A20 inhibits the inflammasome

Review

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Innate immunity in Alzheimer's disease   pp229 - 236
Michael T Heneka, Douglas T Golenbock and Eicke Latz
doi:10.1038/ni.3102
Alzheimer's disease is the most common dementing illness. Heneka, Golenbock and Latz review the inflammatory basis of this disease and the important role played by cells of the innate immune system.

Articles

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Mycobacterium tuberculosis suppresses innate immunity by coopting the host ubiquitin system   pp237 - 245
Jing Wang, Bing-Xi Li, Pu-Pu Ge, Jie Li, Qi Wang et al.
doi:10.1038/ni.3096
PtpA is a secreted mycobacterial protein and virulence factor. Liu and colleagues demonstrate that PtpA suppresses signaling by cells of the innate immune system by coopting the activity of host ubiquitin.

The kinase MST4 limits inflammatory responses through direct phosphorylation of the adaptor TRAF6   pp246 - 257
Shi Jiao, Zhen Zhang, Chuanchuan Li, Min Huang, Zhubing Shi et al.
doi:10.1038/ni.3097
Inflammation needs to be carefully controlled to prevent immunopathology. Zhou and colleagues demonstrate that the kinase MST4 dampens inflammation in a nonredundant way by targeting the activity of the key proinflammatory signaling molecule TRAF6.

αβ T cell antigen receptor recognition of CD1a presenting self lipid ligands   pp258 - 266
Richard W Birkinshaw, Daniel G Pellicci, Tan-Yun Cheng, Andrew N Keller, Maria Sandoval-Romero et al.
doi:10.1038/ni.3098
CD1a presents a broad repertoire of lipid-based antigens. Rossjohn and colleagues show that the TCR docks over CD1a in a manner that precludes contact with permissive antigens, while nonpermissive antigens disrupt the TCR-CD1a contact.

Protein kinase CK2 enables regulatory T cells to suppress excessive TH2 responses in vivo   pp267 - 275
Alexander Ulges, Matthias Klein, Sebastian Reuter, Bastian Gerlitzki, Markus Hoffmann et al.
doi:10.1038/ni.3083
The mechanisms that control the suppressive function of Treg cells in specific tissues are unclear. Bopp and colleagues show that Treg cells have high expression of kinase CK2 and this is critical for their ability to suppress type 2 responses in the lungs.

See also: News and Views by Sawant & Dent

The transcriptional regulators IRF4, BATF and IL-33 orchestrate development and maintenance of adipose tissue-resident regulatory T cells   pp276 - 285
Ajithkumar Vasanthakumar, Kazuyo Moro, Annie Xin, Yang Liao, Renee Gloury et al.
doi:10.1038/ni.3085
Obesity-associated inflammation is restrained by regulatory T cells present in visceral fat. Kallies and colleagues show interleukin 33 and the transcription factors BATF and IRF4 are necessary to maintain visceral adipose tissue Treg cells.

IL-1 signaling modulates activation of STAT transcription factors to antagonize retinoic acid signaling and control the TH17 cell-iTreg cell balance   pp286 - 295
Rajatava Basu, Sarah K Whitley, Suniti Bhaumik, Carlene L Zindl, Trenton R Schoeb et al.
doi:10.1038/ni.3099
iTreg cells and TH17 cells share developmental steps, but their cellular fate depends on environmental cues. Weaver and colleagues show that IL-1 signaling alters the STAT3-STAT5 balance to skew cellular differentiation towards TH17 CD4+ T cells.

See also: News and Views by Villarino & Laurence

Class-switched memory B cells remodel BCRs within secondary germinal centers   pp296 - 305
Louise J McHeyzer-Williams, Pierre J Milpied, Shinji L Okitsu and Michael G McHeyzer-Williams
doi:10.1038/ni.3095
The mechanisms of secondary changes in antibody repertoires remain unclear. McHeyzer-Williams and colleagues define the stages of reentry of class-switched memory B cells into germinal centers to remodel existing antibody specificities.

Resources

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Transcriptional programs define molecular characteristics of innate lymphoid cell classes and subsets   pp306 - 317
Michelle L Robinette, Anja Fuchs, Victor S Cortez, Jacob S Lee, Yaming Wang et al.
doi:10.1038/ni.3094
The classification of some subsets of innate lymphoid cells (ILCs) is unclear. Colonna and colleagues use transcriptional profiling to show unique gene-expression patterns for some ILCs and overlapping patterns between ILC1 and NK cells.

See also: News and Views by Diefenbach

The long intergenic noncoding RNA landscape of human lymphocytes highlights the regulation of T cell differentiation by linc-MAF-4   pp318 - 325
Valeria Ranzani, Grazisa Rossetti, Ilaria Panzeri, Alberto Arrigoni, Raoul J P Bonnal et al.
doi:10.1038/ni.3093
Long intergenic noncoding RNAs (lincRNAs) contribute to the regulation of gene expression. Pagani and colleagues identify hundreds of unique lincRNAs expressed in human lymphocytes and demonstrate a role for the lincRNA linc-MAF-4 in the differentiation of CD4+ T cells.

See also: News and Views by Roux & Lindsay

Corrigenda

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Corrigendum: Intestinal immune homeostasis is regulated by the crosstalk between epithelial cells and dendritic cells   p326
Monica Rimoldi, Marcello Chieppa, Valentina Salucci, Francesca Avogadri, Angelica Sonzogni et al.
doi:10.1038/ni0315-326a

Corrigendum: Direct extracellular interaction between the early secreted antigen ESAT-6 of Mycobacterium tuberculosis and TLR2 inhibits TLR signaling in macrophages   p326
Sushil Kumar Pathak, Sanchita Basu, Kunal Kumar Basu, Anirban Banerjee, Shresh Pathak et al.
doi:10.1038/ni0315-326b

Corrigendum: The RIP1-RIP3 complex initiates mitochondrial fission to fuel NLRP3   p326
Manira Rayamajhi and Edward A Miao
doi:10.1038/ni0315-326c

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