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Morten Lundh Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark
Chemical Biology and Therapeutics Program, Broad Institute of Harvard and MIT, Boston, Massachusetts, USA

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Marco Bugliani Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy

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Tina Dahlby Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark

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Danny Hung-Chieh Chou Chemical Biology and Therapeutics Program, Broad Institute of Harvard and MIT, Boston, Massachusetts, USA

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Bridget Wagner Chemical Biology and Therapeutics Program, Broad Institute of Harvard and MIT, Boston, Massachusetts, USA

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Seyed Mojtaba Ghiasi Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark

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Vincenzo De Tata Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark

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Zhifei Chen Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark

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Marianne Nissan Lund Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark
Department of Food Science, University of Copenhagen, Copenhagen, Denmark

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Michael J Davies Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark

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Piero Marchetti Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy

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Thomas Mandrup-Poulsen Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark

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-proteasome sequences between human and rodents (Ferrington & Gregerson 2012). IFNγ was the driver of i-proteasome expression ( Fig. 2 ) with no detectable potentiation by IL-1β. Accordingly, the Psmb8 and Psmb9 promotors contain interferon consensus sequence 2- and

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-17-0110
Volume/Issue:
Volume 233: Issue 3
Free access
Ashley Patton Department of Specialty Medicine, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA
Diabetes Institute, Ohio University, Athens, Ohio, USA
Department of Biological Sciences, Ohio University, Athens, Ohio, USA
Molecular & Cellular Biology Program, College of Arts and Sciences, Ohio University, Athens, Ohio, USA

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Tyler Church Department of Specialty Medicine, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA
Diabetes Institute, Ohio University, Athens, Ohio, USA

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Caroline Wilson Department of Chemical and Biomolecular Engineering, Russ College of Engineering and Technology, Ohio University, Athens, Ohio, USA

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Jean Thuma Department of Specialty Medicine, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA
Diabetes Institute, Ohio University, Athens, Ohio, USA

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Douglas J Goetz Department of Chemical and Biomolecular Engineering, Russ College of Engineering and Technology, Ohio University, Athens, Ohio, USA
Molecular & Cellular Biology Program, College of Arts and Sciences, Ohio University, Athens, Ohio, USA
Biomedical Engineering Program, Ohio University, Athens, Ohio, USA

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Darlene E Berryman Diabetes Institute, Ohio University, Athens, Ohio, USA
Department of Biomedical Sciences, Ohio University, Athens, Ohio, USA
The Edison Biotechnology Institute, Ohio University, Athens, Ohio, USA

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Edward O List Department of Specialty Medicine, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA
Diabetes Institute, Ohio University, Athens, Ohio, USA
The Edison Biotechnology Institute, Ohio University, Athens, Ohio, USA

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Frank Schwartz Department of Specialty Medicine, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA
Diabetes Institute, Ohio University, Athens, Ohio, USA

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Kelly D McCall Department of Specialty Medicine, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA
Diabetes Institute, Ohio University, Athens, Ohio, USA
Department of Biological Sciences, Ohio University, Athens, Ohio, USA
Molecular & Cellular Biology Program, College of Arts and Sciences, Ohio University, Athens, Ohio, USA
Biomedical Engineering Program, Ohio University, Athens, Ohio, USA
Department of Biomedical Sciences, Ohio University, Athens, Ohio, USA

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-associated membrane protein 1/TIR-domain-containing adapter-inducing interferon-β (TRIF) ( Holland et al . 2011 ). In the MyD88-dependent pathway, MyD88 signals the activation of IL-1 receptor-associated kinases (IRAK4/IRAK1) and TNF receptor-associated factor (TRAF6

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-18-0078
Volume/Issue:
Volume 237: Issue 3
Open access
Shisan Xu Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Fangjing Xie Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Li Tian Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Samane Fallah Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Fatemeh Babaei Department of Chemistry, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Sinai H C Manno Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Francis A M Manno III School of Biomedical Engineering, Faculty of Engineering, University of Sydney, Sydney, New South Wales, Australia

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Lina Zhu Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Kin Fung Wong Department of Biomedical Engineering, Polytechnic University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Yimin Liang Department of Chemistry, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Rajkumar Ramalingam Department of Chemistry, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Lei Sun Department of Biomedical Engineering, Polytechnic University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Xin Wang Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Robert Plumb Waters Technologies Corporation, Milford, Massachusetts, USA

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Lee Gethings Waters Technologies Corporation, Milford, Massachusetts, USA

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Yun Wah Lam Department of Chemistry, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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Shuk Han Cheng Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Hong Kong SAR, People’s Republic of China
State Key Laboratory of Marine Pollution (SKLMP) at City University of Hong Kong, Hong Kong SAR, People’s Republic of China
Department of Materials Science and Engineering, College of Science and Engineering, City University of Hong Kong, Hong Kong SAR, People’s Republic of China

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and neutrophil chemotaxis were upregulated in estrogen-treated males. Among the genes whose expression level in injured hearts were sexually dimorphic, and/or reciprocally regulated by E2 and tamoxifen, were interferon-gamma ( ifn-γ ), interferon

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-19-0413
Volume/Issue:
Volume 245: Issue 1
Open access
Toyoshi Endo Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo City, Yamanashi 409-3898, Japan

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Tetsuro Kobayashi Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo City, Yamanashi 409-3898, Japan

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infiltration in the thyroid ( Dayan & Daniels 1996 ). The appearance of MHC class II molecules on thyroid cells which has been correlated with γ-interferon-containing T cells ( Bottazzo et al . 1983 ), has been thought to be the initiating factor in chronic

Article Type:
Research Article
DOI:
https://doi.org/10.1677/JOE-09-0089
Volume/Issue:
Volume 202: Issue 2
Open access
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Jessica D Bishop Department of Biochemistry and Molecular Biology and
Department of Obstetrics and Gynecology, Dalhousie University, 5850 College Street, Halifax, Nova Scotia, B3H 1X5 Canada

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Wei Lun Nien Department of Biochemistry and Molecular Biology and
Department of Obstetrics and Gynecology, Dalhousie University, 5850 College Street, Halifax, Nova Scotia, B3H 1X5 Canada

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Shauna M Dauphinee Department of Biochemistry and Molecular Biology and
Department of Obstetrics and Gynecology, Dalhousie University, 5850 College Street, Halifax, Nova Scotia, B3H 1X5 Canada

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Catherine K L Too Department of Biochemistry and Molecular Biology and
Department of Obstetrics and Gynecology, Dalhousie University, 5850 College Street, Halifax, Nova Scotia, B3H 1X5 Canada

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interferon regulatory factor-1 (IRF-1) promoter activity ( Boudreau et al. 2002 ). IRF-1 is an immediate-early PRL-responsive gene in lymphoid cells ( Yu-Lee et al. 1990 ). PRL signals primarily through the PRLR-associated Jak2 tyrosine kinase

Article Type:
Research Article
DOI:
https://doi.org/10.1677/joe.1.06368
Volume/Issue:
Volume 190: Issue 2
Free access
Emmely M de Vries Department of Endocrinology and Metabolism, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands

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Eric Fliers Department of Endocrinology and Metabolism, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands

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Anita Boelen Department of Endocrinology and Metabolism, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands

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6 knock out mice show a less pronounced drop in serum T 3 during illness ( Boelen et al . 1996 ). However, acute injection of cytokines failed to induce NTIS like features, except for interferon gamma (IFNγ) which reduces serum T 3 and T 4

Article Type:
Review Article
DOI:
https://doi.org/10.1530/JOE-15-0133
Volume/Issue:
Volume 225: Issue 3
Free access
Marnix Gorissen Department of Organismal Animal Physiology, The Clayton Foundation Laboratories for Peptide Biology, Faculty of Science, Radboud University Nijmegen, Heyendaalseweg 135, 6525AJ Nijmegen, The Netherlands

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Erik de Vrieze Department of Organismal Animal Physiology, The Clayton Foundation Laboratories for Peptide Biology, Faculty of Science, Radboud University Nijmegen, Heyendaalseweg 135, 6525AJ Nijmegen, The Netherlands

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Gert Flik Department of Organismal Animal Physiology, The Clayton Foundation Laboratories for Peptide Biology, Faculty of Science, Radboud University Nijmegen, Heyendaalseweg 135, 6525AJ Nijmegen, The Netherlands

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Mark O Huising Department of Organismal Animal Physiology, The Clayton Foundation Laboratories for Peptide Biology, Faculty of Science, Radboud University Nijmegen, Heyendaalseweg 135, 6525AJ Nijmegen, The Netherlands
Department of Organismal Animal Physiology, The Clayton Foundation Laboratories for Peptide Biology, Faculty of Science, Radboud University Nijmegen, Heyendaalseweg 135, 6525AJ Nijmegen, The Netherlands

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/signal transducer and activator of transcription (JAK/STAT) pathway, ultimately leading to changes in gene expression. Since its discovery as a regulator of interferon (IFN) responses in the immune system ( Schindler et al . 1992 , Darnell et al . 1994 ), JAK

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-11-0033
Volume/Issue:
Volume 209: Issue 2
Free access
Sarah J Richardson Islet Biology Group, Exeter Centre for Excellence in Diabetes (EXCEED), Institute of Biomedical and Clinical Sciences (IBCS), University of Exeter, RILD Level 4, Exeter, UK

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Alberto Pugliese Division of Diabetes Endocrinology and Metabolism, Departments of Medicine, Microbiology and Immunology, Diabetes Research Institute, Leonard Miller School of Medicine, University of Miami, Miami, Florida, USA

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in the T1D pancreas, but not in IDIs or in control pancreas ( Colli et al. 2018 , Osum et al. 2018 ). PDL1 expression in beta cells has been linked to interferon alpha and gamma, in the context of alterations induced by islet inflammation, and is

Article Type:
Review Article
Collections:
100 years of insulin: A special collection, Top-cited articles of 2023
DOI:
https://doi.org/10.1530/JOE-21-0358
Volume/Issue:
Volume 252: Issue 2
Free access
Richard R Almon Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of
Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of
Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of

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Debra C DuBois Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of
Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of

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William Lai Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of

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Bai Xue Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of

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Jing Nie Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of

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William J Jusko Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of
Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics and Life Sciences, Departments of

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examined. Adding to the picture of chronic inflammation in the GK rats are the expression patterns of two interferon-induced genes: Fig. 6 B, interferon-induced protein with tetratricopeptide repeats 1 ( Ifit1 ) and Fig. 6 C, interferon-inducible GTPase

Article Type:
Research Article
DOI:
https://doi.org/10.1677/JOE-08-0404
Volume/Issue:
Volume 200: Issue 3
Free access
Mark O Huising Department of Animal Physiology, Institute for Neuroscience, Radboud University, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands
Department of Cell Biology and Immunology, Wageningen University, Wageningen, The Netherlands

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Corine P Kruiswijk Department of Animal Physiology, Institute for Neuroscience, Radboud University, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands
Department of Cell Biology and Immunology, Wageningen University, Wageningen, The Netherlands

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Gert Flik Department of Animal Physiology, Institute for Neuroscience, Radboud University, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands
Department of Cell Biology and Immunology, Wageningen University, Wageningen, The Netherlands

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-helices, designated helix A–D (Fig. 1 ); their primary amino acid sequences share little to no sequence similarity. Their common fold separates class-I helical cytokines from other cytokines. For example, class-II helical cytokine molecules (interferons (IFNs

Article Type:
Review Article
DOI:
https://doi.org/10.1677/joe.1.06591
Volume/Issue:
Volume 189: Issue 1
Free access