Search from over 60,000 research works

Advanced Search

How to perform aggregometry and lumi-aggregometry in mouse platelets

[thumbnail of Mouse platelets review Platelets 2018 REVISION v1.pdf]
Preview
[thumbnail of Figures]
Preview
Platelets review figs REVISION.pdf - Accepted Version (109kB) | Preview
Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email

Hughes, C. E. orcid id iconORCID: https://orcid.org/0000-0002-9790-5820 (2018) How to perform aggregometry and lumi-aggregometry in mouse platelets. Platelets, 29 (7). pp. 638-643. ISSN 0953-7104 doi: 10.1080/09537104.2018.1478074

Abstract/Summary

Light transmission aggregometry (LTA) and lumi-aggregometry are the gold standard platelet assays both clinically and for basic research. The availability of different strains of genetically modified mice, and mouse models of human disease means that often laboratories need to use mouse platelets in these assays. Overall, performing aggregometry and lumi-aggregometry with mouse platelets is similar to with human platelets, although methods need be adapted to accommodate their small size, reduced blood volume and different protein levels. This review aims to highlight these key considerations when planning aggregometry experiments with mouse platelets. These include the method of taking blood, including the use of anticoagulants, as well as the method of platelet preparation, and how to maximise yields. This review also covers how to maximise the number of aggregations that can be performed, both by understanding the minimum requirements of your aggregometer, or by considering new approaches. These include employing high throughput plate-based aggregometry (Optimul), or the use of TPO-mimetics to stimulate platelet production in mice to boost their platelet counts. Finally, phenotypic differences between mouse and human platelets, such as protein expression or sensitivity to agonists is discussed as an important consideration when planning experiments.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/77089
Item Type Article
Refereed Yes
Divisions Life Sciences > School of Biological Sciences > Biomedical Sciences
Publisher Taylor & Francis
Download/View statistics View download statistics for this item

Downloads

Downloads per month over past year

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar