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Cardiovascular Diabetology | 2006

Human epicardial adipose tissue expresses a pathogenic profile of adipocytokines in patients with cardiovascular disease

Adam R. Baker; Nancy F. da Silva; David W. Quinn; A. L. Harte; Domenico Pagano; Robert S. Bonser; S. Kumar; Philip G. McTernan

IntroductionInflammation contributes to cardiovascular disease and is exacerbated with increased adiposity, particularly omental adiposity; however, the role of epicardial fat is poorly understood.MethodsFor these studies the expression of inflammatory markers was assessed in epicardial fat biopsies from coronary artery bypass grafting (CABG) patients using quantitative RT-PCR. Further, the effects of chronic medications, including statins, as well as peri-operative glucose, insulin and potassium infusion, on gene expression were also assessed. Circulating resistin, CRP, adiponectin and leptin levels were determined to assess inflammation.ResultsThe expression of adiponectin, resistin and other adipocytokine mRNAs were comparable to that in omental fat. Epicardial CD45 expression was significantly higher than control depots (p < 0.01) indicating significant infiltration of macrophages. Statin treated patients showed significantly lower epicardial expression of IL-6 mRNA, in comparison with the control abdominal depots (p < 0.001). The serum profile of CABG patients showed significantly higher levels of both CRP (control: 1.28 ± 1.57 μg/mL vs CABG: 9.11 ± 15.7 μg/mL; p < 0.001) and resistin (control: 10.53 ± 0.81 ng/mL vs CABG: 16.8 ± 1.69 ng/mL; p < 0.01) and significantly lower levels of adiponectin (control: 29.1 ± 14.8 μg/mL vs CABG: 11.9 ± 6.0 μg/mL; p < 0.05) when compared to BMI matched controls.ConclusionEpicardial and omental fat exhibit a broadly comparable pathogenic mRNA profile, this may arise in part from macrophage infiltration into the epicardial fat. This study highlights that chronic inflammation occurs locally as well as systemically potentially contributing further to the pathogenesis of coronary artery disease.


Proceedings of the National Academy of Sciences of the United States of America | 2012

Genome sequence of the button mushroom Agaricus bisporus reveals mechanisms governing adaptation to a humic-rich ecological niche

Emmanuelle Morin; Annegret Kohler; Adam R. Baker; Marie Foulongne-Oriol; Vincent Lombard; László G. Nagy; Robin A. Ohm; Aleksandrina Patyshakuliyeva; Annick Brun; Andrea Aerts; Andy M. Bailey; Christophe Billette; Pedro M. Coutinho; Greg Deakin; Harshavardhan Doddapaneni; Dimitrios Floudas; Jane Grimwood; Kristiina Hildén; Ursula Kües; Kurt LaButti; Alla Lapidus; Erika Lindquist; Susan Lucas; Claude Murat; Robert Riley; Asaf Salamov; Jeremy Schmutz; Venkataramanan Subramanian; Han A. B. Wösten; Jianping Xu

Agaricus bisporus is the model fungus for the adaptation, persistence, and growth in the humic-rich leaf-litter environment. Aside from its ecological role, A. bisporus has been an important component of the human diet for over 200 y and worldwide cultivation of the “button mushroom” forms a multibillion dollar industry. We present two A. bisporus genomes, their gene repertoires and transcript profiles on compost and during mushroom formation. The genomes encode a full repertoire of polysaccharide-degrading enzymes similar to that of wood-decayers. Comparative transcriptomics of mycelium grown on defined medium, casing-soil, and compost revealed genes encoding enzymes involved in xylan, cellulose, pectin, and protein degradation are more highly expressed in compost. The striking expansion of heme-thiolate peroxidases and β-etherases is distinctive from Agaricomycotina wood-decayers and suggests a broad attack on decaying lignin and related metabolites found in humic acid-rich environment. Similarly, up-regulation of these genes together with a lignolytic manganese peroxidase, multiple copper radical oxidases, and cytochrome P450s is consistent with challenges posed by complex humic-rich substrates. The gene repertoire and expression of hydrolytic enzymes in A. bisporus is substantially different from the taxonomically related ectomycorrhizal symbiont Laccaria bicolor. A common promoter motif was also identified in genes very highly expressed in humic-rich substrates. These observations reveal genetic and enzymatic mechanisms governing adaptation to the humic-rich ecological niche formed during plant degradation, further defining the critical role such fungi contribute to soil structure and carbon sequestration in terrestrial ecosystems. Genome sequence will expedite mushroom breeding for improved agronomic characteristics.


The Journal of Clinical Endocrinology and Metabolism | 2009

Epicardial Adipose Tissue as a Source of Nuclear Factor-κB and c-Jun N-Terminal Kinase Mediated Inflammation in Patients with Coronary Artery Disease

Adam R. Baker; A. L. Harte; N. Howell; D. C. Pritlove; Aaron M. Ranasinghe; N. F. da Silva; E. M. Youssef; Kamlesh Khunti; Melanie J. Davies; Robert S. Bonser; S. Kumar; Domenico Pagano; P. G. McTernan

CONTEXT Visceral adipose tissue (AT) is known to confer a significantly higher risk of type 2 diabetes and cardiovascular disease. Epicardial AT has been shown to be related to cardiovascular disease and myocardial function through unidentified mechanisms. Epicardial AT expresses an inflammatory profile of proteins; however, the mechanisms responsible are yet to be elucidated. OBJECTIVES The objectives of the study were to: 1) examine key mediators of the nuclear factor-kappaB (NFkappaB) and c-Jun N-terminal kinase (JNK) pathways in paired epicardial and gluteofemoral (thigh) AT from coronary artery disease (CAD) and control patients and 2) investigate circulating endotoxin levels in CAD and control subjects. DESIGN Serums and AT biopsies (epicardial and thigh) were obtained from CAD (n = 16) and non-CAD (n = 18) patients. Inflammation was assessed in tissue and serum samples through Western blot, real-time PCR, ELISAs, and activity studies. RESULTS Western blotting showed epicardial AT had significantly higher NFkappaB, inhibitory-kappaB kinase (IKK)-gamma, IKKbeta, and JNK-1 and -2 compared with thigh AT. Epicardial mRNA data showed strong correlations between CD-68 and toll-like receptor-2, toll-like receptor-4, and TNF-alpha. Circulating endotoxin was elevated in patients with CAD compared with matched controls [CAD: 6.80 +/- 0.28 endotoxin unit(EU)/ml vs. controls: 5.52 +/- 0.57 EU/ml; P<0.05]. CONCLUSION Epicardial AT from patients with CAD shows increased NFkappaB, IKKbeta, and JNK expression compared with both CAD thigh AT and non-CAD epicardial AT, suggesting a depot-specific as well as a disease-linked response to inflammation. These studies implicate both NFkappaB and JNK pathways in the inflammatory profile of epicardial AT and highlight the role of the macrophage in the inflammation within this tissue.


BMC Genomics | 2013

Carbohydrate utilization and metabolism is highly differentiated in Agaricus bisporus

Aleksandrina Patyshakuliyeva; Edita Jurak; Annegret Kohler; Adam R. Baker; Evy Battaglia; Wouter J.C. de Bruijn; Kerry S. Burton; Michael P. Challen; Pedro M. Coutinho; Daniel C. Eastwood; Birgit S. Gruben; Miia R. Mäkelä; Francis L. Martin; Marina Nadal; Joost van den Brink; Ad Wiebenga; Miaomiao Zhou; Bernard Henrissat; Mirjam A. Kabel; Harry Gruppen; Ronald P. de Vries

BackgroundAgaricus bisporus is commercially grown on compost, in which the available carbon sources consist mainly of plant-derived polysaccharides that are built out of various different constituent monosaccharides. The major constituent monosaccharides of these polysaccharides are glucose, xylose, and arabinose, while smaller amounts of galactose, glucuronic acid, rhamnose and mannose are also present.ResultsIn this study, genes encoding putative enzymes from carbon metabolism were identified and their expression was studied in different growth stages of A. bisporus. We correlated the expression of genes encoding plant and fungal polysaccharide modifying enzymes identified in the A. bisporus genome to the soluble carbohydrates and the composition of mycelium grown compost, casing layer and fruiting bodies.ConclusionsThe compost grown vegetative mycelium of A. bisporus consumes a wide variety of monosaccharides. However, in fruiting bodies only hexose catabolism occurs, and no accumulation of other sugars was observed. This suggests that only hexoses or their conversion products are transported from the vegetative mycelium to the fruiting body, while the other sugars likely provide energy for growth and maintenance of the vegetative mycelium. Clear correlations were found between expression of the genes and composition of carbohydrates. Genes encoding plant cell wall polysaccharide degrading enzymes were mainly expressed in compost-grown mycelium, and largely absent in fruiting bodies. In contrast, genes encoding fungal cell wall polysaccharide modifying enzymes were expressed in both fruiting bodies and vegetative mycelium, but different gene sets were expressed in these samples.


Archive | 2007

The effects adiposity, diabetic status and depot-specificity on the activation of NFKB on JNK in human abdominal adipose tissue

Christine M. Kusminski; N. F. da Silva; Anne E. Fowler; S. J. Creely; A. L. Harte; Adam R. Baker; Thomas Billyard; J. Paul O'Hare; S. Kumar; P. G. McTernan

The President reported that ‘The case for a UN resolution’ had been prepared by the IDF to highlight the need for a United Nations Resolution on diabetes in order to focus attention on the need to stop the growing diabetes epidemic. Dr. Ferrannini reported that ISPAD was a small, but enthusiastic organisation which had recently held a very well-attended meeting in Cambridge, UK. Following information that pediatricians are not attending the EASD Annual Meetings, discussions to organise a pediatric track in the programme of the Annual Meeting have been put forward. Dr. DahlJørgensen has also suggested organising a joint EASD/ ISPAD Postgraduate Course on Pediatric Diabetes in Europe in 2008. The President reported that a joint statement with ADA on guidelines on the treatment of type 2 diabetes was simultaneously published in August in both Diabetologia and Diabetes Care. Drs. R.J. Heine and R. Holman lead an ad-hoc committee from the EASD which also included Dr. S. del Prato and Dr. U. Smith. More details on EASD and EFSD activities were reported in the President’s Address given before the Minkowski Lecture, which is available on the internet under: http://www.easd-lectures.org/copenhagen/index. php?menu=lectures&id=66 and in his speech before the 38th Claude Bernard Lecture, available under: http://www.easd-lectures.org/copenhagen/index. php?menu=lectures&id=72 The President welcomed everyone to the 42nd General Assembly.Type III phosphatidylinositol 4-kinases mediate plasma membrane PIP2 synthesis in insulin-secreting cells


Proceedings of the National Academy of Sciences of the United States of America | 2012

Correction for Genome sequence of the button mushroom Agaricus bisporus reveals mechanisms governing adaptation to a humic-rich ecological niche (vol 109, pg 17501, 2012)

Emmanuelle Morin; Annegret Kohler; Adam R. Baker; Marie Foulongne Oriol; Julien Lombard; László Nagy; Robin A. Ohm; Aleksandrina Patyshakuliyeva; Annick Brun-Jacob; Andrea Aerts; Andy M. Bailey; Christophe Billette; Pedro M. Coutinho; Greg Deakin; Harshavardhan Doddapaneni; Dimitrios Floudas; Jane Grimwood; Kristiina Hildén; Ursula Kües; Kurt LaButti; Alla Lapidus; Erika Lindquist; Susan Lucas; Claude Murat-Furminieux; Robert Riley; Asaf Salamov; Jeremy Schmutz; Venkataramanan Subramanian; Han A. B. Wösten; Jianping Xu


Mushroom biology and mushroom products. Proceedings of the 7th International Conference on Mushroom Biology and Mushroom Products, Arcachon, France, 4-7 October, 2011. Volume 1. Oral presentations. | 2011

MUSHROOM VIRUS X - THE IDENTIFICATION OF BROWN CAP MUSHROOM VIRUS AND A NEW HIGHLY SENSITIVE DIAGNOSTIC TEST FOR PHASE III COMPOST

Kerry S. Burton; Julian Green; Adam R. Baker; Daniel C. Eastwood; Helen Grogan


Archive | 2008

Epicardial adipose tissue as a source of NFκB and JNK mediated inflammation in patients with coronary artery disease.

Adam R. Baker; Al Harte; N Howell; Dc Pritlove; Em Youssef; K Khunti; S Kumar; D Pagano


Archive | 2007

DPP-IV inhibitors influence fat metabolism through modulation of NPY's paracrine antilipolytic action in adipose tissue

Katarina Kos; Adam R. Baker; A. L. Harte; J. Paul O'Hare; P. G. McTernan; S. Kumar


Archive | 2009

Disease N-Terminal Kinase Mediated Inflammation in Patients with Coronary Artery Epicardial Adipose Tissue as a Source of Nuclear Factor-{kappa}B and c-Jun

S. Kumar; Domenico Pagano; P. G. McTernan; Adam R. Baker; A. L. Harte; N. Howell; D. C. Pritlove; Aaron M. Ranasinghe; N. F. da Silva; E. M. Youssef; Kamlesh Khunti

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S. Kumar

University of Warwick

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Sudhesh Kumar

Queen Elizabeth Hospital Birmingham

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