Publications by authors named "Heather Mathie"

Article Synopsis
  • The article discusses the coexpression of CCR1 and CCR2 on monocytes, highlighting that this combination is essential in identifying a unique subpopulation of these immune cells.
  • The authors acknowledge that Fabian Schuette was omitted from the initial author list and have corrected this oversight in the online version of the article.
  • The research was conducted by a team from the Chemokine Research Group at the University of Glasgow, focusing on the role of chemokines in immune response.
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The interactions between chemokines and their receptors, particularly in the context of inflammation, are complex, with individual receptors binding multiple ligands and individual ligands interacting with multiple receptors. In addition, there are numerous reports of simultaneous coexpression of multiple inflammatory chemokine receptors on individual inflammatory leukocyte subtypes. Overall, this has previously been interpreted as redundancy and proposed as a protective mechanism to ensure that the inflammatory response is robust.

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The bovine afferent lymphatic cannulation model allows collection of large volumes of afferent lymph and provides an opportunity to study lymphatic cells trafficking from the periphery directly ex-vivo. The technique requires surgical intervention, but influence of the procedure or time post-surgery on cells trafficking in the lymph has not been well documented. Here, we measured the volume of lymph and number of cells/mL collected daily over a two week time-course.

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Article Synopsis
  • Cattle in Scotland serve as a reservoir for Shiga toxin-producing (STEC) pathogens, contributing to higher rates of STEC infections among humans compared to the European average.
  • A study collected and analyzed fecal samples from 110 herds, revealing varying herd-level prevalence rates for non-O157 serogroups O26, O103, O111, and O145, with O26 being the most common.
  • Seasonal and regional differences were noted, with higher prevalence of certain serogroups in the South West during autumn, and a lack of positive herds associated with Central Scotland and winter.
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Quantification of Mycobacterium avium subspecies paratuberculosis (MAP) during in vitro infection experiments is challenging due to limitations of currently utilised methods, such as colony counting. Here we describe quantifying MAP infection of bovine macrophages (Mφ) using confocal microscopy. Bovine monocyte derived macrophages were infected with MAP at a high or low dose and the number of intracellular bacteria calculated at 2 h post infection using confocal microscopy.

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