Richard W. McLaughlin
McGill University
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Publication
Featured researches published by Richard W. McLaughlin.
Journal of Clinical Microbiology | 2002
Richard W. McLaughlin; Hojatollah Vali; Peter C. K. Lau; Roger G. E. Palfree; Angela De Ciccio; Marc Sirois; Darakhshan Ahmad; Richard Villemur; Marcel Desrosiers; Eddie C. S. Chan
ABSTRACT Dark-field microscopy of blood from healthy individuals revealed the existence of pleomorphic microorganisms. These bacteria exhibited limited growth and susceptibility to antibiotics and could be detected by fluorescent in situ hybridization and flow cytometry. They were further characterized by analysis of their 16S rRNA and gyrB genes.
Neurobiology of Aging | 2006
Giovanna Sebastiani; Céline Morissette; Caroline Lagacé; Marie Boulé; Marie-Josée Ouellette; Richard W. McLaughlin; Diane Lacombe; Francine Gervais; Patrick Tremblay
Microglial activation is a key player in the degenerative process that accompanies the deposition of amyloid-beta (Abeta) peptide into senile plaques in Alzheimers disease (AD) patients. The goal of this study is to identify novel genes involved in microglial activation in response to Abeta peptide. Prompted by the fact that soluble Abeta(1-42) (sAbeta(1-42))-stimulated primary rat microglia produce more tumor necrosis factor-alpha (TNF-alpha) than fibrillar Abeta(1-42) (fAbeta(1-42))-stimulated microglia, we examined gene expression in these cells following stimulation using cDNA arrays. This analysis confirms the upregulation caused by both sAbeta(1-42) and fAbeta(1-42) of pro-inflammatory molecules such as TNF-alpha, interleukin-1beta and macrophage inflammatory protein-1alpha. In addition, other transcripts not previously described in the context of Abeta-induced microglial activation were identified. The modulation of some of these genes within microglial cells seems to be specific to sAbeta(1-42) as compared to fAbeta(1-42) suggesting that different forms of Abeta may activate distinct pathways during the progression of AD. Importantly, we demonstrate that Pde4B, a cAMP-specific phosphodiesterase, is upregulated by Abeta and results in an increased production of TNF-alpha. Inhibition of Pde4B reduces by up to 70% the release of TNF-alpha from sAbeta-stimulated microglial cells, implicating cAMP as an important mediator of Abeta-induced microglial activation.
Journal of Clinical Microbiology | 2002
Dalius J. Briedis; Ali Khamessan; Richard W. McLaughlin; Hojatollah Vali; Maria Panaritou; Eddie C. S. Chan
ABSTRACT Campylobacter fetus subsp. fetus is a gram-negative, slender, spirally curved bacterial pathogen. It has been isolated from human blood, spinal fluid, and abscesses, but cellulitis associated with bacteremia is rare. We report its isolation from a blood culture of a human patient with cellulitis as well as difficulties encountered in determining the identity of the subspecies of C. fetus.
Neuroreport | 1999
Richard W. McLaughlin; N. M. K. Ng Ying Kin; Moy Fong Chen; N. P. V. Nair; Eddie C. S. Chan
It has been reported previously that spirochetes could be one of the causes of Alzheimers disease (AD). In this study, we have attempted to reproduce these findings by examining fresh blood samples from 22 patients diagnosed with early stage (n = 16) and late stage (n = 6) AD. The patients were participants in a clinical drug trial. Fresh necropsy brain cortical specimens from AD patients (n = 7) were also examined. Spirochetes were observed microscopically in the blood of only one late-stage AD patient. None of the brain tissues showed the presence of spirochetes. Our results suggest that spirochetes are probably not associated with AD.
Microscopy and Microanalysis | 2014
Neal Magdefrau; Julie Wittenzellner; Daniel G. Goberman; Richard W. McLaughlin; Sreenivas Bhattiprolu
The introduction of improved, large area silicon drift detector (SDD) technology for energy dispersive spectrometry (EDS) along with advances in focused ion beam (FIB) techniques provides for a unique opportunity to perform chemical analysis of fine structures in 3-D. The improvements in data collection efficiency, increased count rates and better computing power enables routine collection of 3D EDS datasets for materials science applications.
Journal of Biological Chemistry | 2003
Robert Chalifour; Richard W. McLaughlin; Louis Lavoie; Céline Morissette; Nadine Tremblay; Marie Boulé; Philippe Sarazin; Dino Stéa; Diane Lacombe; Patrick Tremblay; Francine Gervais
Oral Microbiology and Immunology | 2000
Eddie C. S. Chan; Richard W. McLaughlin
Archive | 2004
Patrick Tremblay; Richard W. McLaughlin
Oral Microbiology and Immunology | 1999
A. De Ciccio; Richard W. McLaughlin; Eddie C. S. Chan
Archive | 2004
Patrick Tremblay; Richard W. McLaughlin