David M. Thomson

ORCID: 0000-0002-3318-7137
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About
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Research Areas
  • Metabolism, Diabetes, and Cancer
  • Adipose Tissue and Metabolism
  • Immunotherapy and Immune Responses
  • Monoclonal and Polyclonal Antibodies Research
  • Muscle Physiology and Disorders
  • Pancreatic function and diabetes
  • Immune Cell Function and Interaction
  • Glycosylation and Glycoproteins Research
  • Mitochondrial Function and Pathology
  • Muscle metabolism and nutrition
  • Diet and metabolism studies
  • Macrophage Migration Inhibitory Factor
  • Cancer Immunotherapy and Biomarkers
  • RNA Interference and Gene Delivery
  • Neuroscience and Neuropharmacology Research
  • Cancer Research and Treatments
  • Exercise and Physiological Responses
  • Phagocytosis and Immune Regulation
  • Pancreatic and Hepatic Oncology Research
  • Asthma and respiratory diseases
  • Receptor Mechanisms and Signaling
  • Pneumocystis jirovecii pneumonia detection and treatment
  • Radiopharmaceutical Chemistry and Applications
  • T-cell and B-cell Immunology
  • Genetics and Neurodevelopmental Disorders

Brigham Young University
2014-2025

University of Strathclyde
2010-2023

Montreal General Hospital
1985-2019

McGill University
1982-2019

Edinburgh Royal Infirmary
2015

University of Edinburgh
2015

University of Glasgow
2010

East Carolina University
2005-2008

Piedmont International University
2006

H.T. Harvey & Associates
2001

A radioimmunoassay has been developed for determining the serum levels of carcinoembryonic antigen human digestive system in patients with cancer colon and rectum. The assay is simple to perform a high degree reproducibility specificity. test detects concentration 2.5 ng per ml this provided first demonstration circulating tumor-specific sera patients.

10.1073/pnas.64.1.161 article EN Proceedings of the National Academy of Sciences 1969-09-01

AMP-activated protein kinase (AMPK) has been identified as a regulator of gene transcription, increasing mitochondrial proteins oxidative metabolism well hexokinase expression in skeletal muscle. In mice, muscle-specific knockout LKB1, component the upstream AMPK, prevents contraction- and 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR)-induced activation AMPK muscle, increase II that is normally observed with chronic AICAR AMPK. Since previous reports show cAMP response...

10.1152/japplphysiol.00900.2007 article EN Journal of Applied Physiology 2007-12-07

Regulation of protein translation through Akt and the downstream mammalian target rapamycin (mTOR) pathway is an important component cellular response to hypertrophic stimuli. It has been proposed that 5'-AMP-activated kinase (AMPK) activation during muscle contraction may limit resistance-type exercise by inhibiting translational signaling. However, experimental manipulation AMPK activity such a stimulus not attempted. Therefore, we investigated whether can attenuate signaling Akt/mTOR...

10.1152/japplphysiol.00915.2007 article EN Journal of Applied Physiology 2008-01-11

A unique property of skeletal muscle is its ability to adapt mass changes in activity. Inactivity, as disuse or aging, causes atrophy, the loss and strength, leading physical incapacity poor quality life. Here, through a combination transcriptomics transgenesis, we identify sestrins, family stress-inducible metabolic regulators, protective factors against wasting. Sestrin expression decreases during inactivity genetic deficiency exacerbates wasting; conversely, sestrin overexpression...

10.1038/s41467-019-13832-9 article EN cc-by Nature Communications 2020-01-13

14-3-3ζ promotes cell survival via dynamic interactions with a vast network of binding partners, many which are involved in stress regulation. We show here that hypoxia (low glucose and oxygen) triggers rearrangement the interactome to favor an interaction core autophagy regulator Atg9A. Our data suggest localization mammalian Atg9A autophagosomes requires phosphorylation on C terminus at S761, creates docking site. Under basal conditions, this is maintained low level dependent both ULK1...

10.1128/mcb.00740-14 article EN Molecular and Cellular Biology 2014-09-30

LKB1 has been identified as a component of the major upstream kinase AMP-activated protein (AMPK) in skeletal muscle. To investigate roles muscle, we used muscle-specific knockout (MLKB1KO) mice that exhibit low expression heart and but not other tissues. The importance muscle physiology was demonstrated by observation electrical stimulation situ increased AMPK phosphorylation activity wild-type (WT) LKB1KO mice. Likewise, acetyl-CoA carboxylase (ACC) markedly attenuated KO had difficulty...

10.1152/ajpendo.00366.2006 article EN AJP Endocrinology and Metabolism 2006-08-23

Skeletal muscle mass declines with age, as does the potential for overload-induced fast-twitch skeletal hypertrophy. Because 5′-AMP-activated protein kinase (AMPK) activity is thought to inhibit synthesis and may therefore modulate hypertrophy, purpose of this investigation was examine AMPK phosphorylation status (a marker activity) its association attenuated hypertrophy observed in aged muscle. One-week overload plantaris slow-twitch soleus muscles achieved young adult (8 mo; n = 7) old (30...

10.1152/japplphysiol.00811.2004 article EN Journal of Applied Physiology 2005-01-12

Abstract The peripheral blood monocyte is the reactive cell in tube LAI assay. loses its properties of adherence to glass upon exposure specific antigen. Two different experiments determine if lymphocytes, when they reacted with tumour, released mediators that were responsible for inhibiting adherence, gave negative results. mechanism whereby tumour antigen appeared be recognized was binding cytophilic IgG anti‐tumour antibody receptors on surface monocyte. results indicate normal monocytes...

10.1002/ijc.2910180108 article EN International Journal of Cancer 1976-07-15

Lipid metabolism is important for health and insulin action, yet the fundamental process of regulating lipid during muscle contraction incompletely understood. Here, we show that liver kinase B1 (LKB1) muscle-specific knockout (LKB1 MKO) mice display decreased fatty acid (FA) oxidation treadmill exercise. LKB1 MKO also SIK3 activity, increased histone deacetylase 4 expression, NAD+ concentration SIRT1 expression genes involved in FA oxidation. In AMP-activated protein (AMPK)α2 KO mice,...

10.2337/db12-1160 article EN cc-by-nc-nd Diabetes 2013-01-25

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10.1177/003591571400700505 article EN Proceedings of the Royal Society of Medicine 1914-04-01

Impaired overload-induced protein synthesis and growth in aged fast-twitch skeletal muscle may result from diminished responsiveness of signalling intermediates controlling translation. Yet, potential age-related decrements have never been examined direct parallel with impaired any model. To this end, we used Western blotting to examine the contents phosphorylation states mammalian target rapamycin (mTOR) its downstream translational intermediates, 70 kDa ribosomal S6 kinase (S6k), (rpS6),...

10.1113/jphysiol.2006.107490 article EN The Journal of Physiology 2006-04-21

Abstract Leukocytes from patients with limited cancer display LAI reactivity whereas leukocytes metastatic frequently demonstrate no in the tube assay. The (monocytes) of reactive react tumour antigen through specific cytophilic anti‐tumour IgG antibody bound to monocyte's Fc cell surface receptors. non‐reactive monocytes advanced lacked ability bind free antibody. Moreover, serum patient contained capable “arming” normal leukocytes. large burdens antigenic determinants absorbing or when...

10.1002/ijc.2910180109 article EN International Journal of Cancer 1976-07-15

Abstract Peripheral blood leukocytes (PBL) from breast cancer patients with early or localized fail to adhere glass in the presence of extract. The same do not react unrelated tumour extracts. Enrichment and depletion certain PBL populations apparently indicated that indicator and/or reactive cell manifesting non‐adherence appropriate antigen was phagocytic, adherent absence had surface Fc‐receptors. involved, therefore, appears be circulating monocyte. These results show tube LAI assay,...

10.1002/ijc.2910180107 article EN International Journal of Cancer 1976-07-15

10.1177/003591571400700509 article EN Proceedings of the Royal Society of Medicine 1914-04-01
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