| Autor: |
Davenport P; Division of Newborn Medicine., Lorenz V; Division of Newborn Medicine., Liu ZJ; Division of Newborn Medicine., Feldman HA; Institutional Centers for Clinical and Translational Research, Boston Children's Hospital, Boston, MA, USA., Canas J; Division of Newborn Medicine., Nolton E; Division of Newborn Medicine., Badur CA; Division of Newborn Medicine., Do TM; Division of Newborn Medicine., Sola-Visner M; Division of Newborn Medicine. |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc [J Vet Diagn Invest] 2021 Sep; Vol. 33 (5), pp. 913-919. Date of Electronic Publication: 2021 Jul 05. |
| DOI: |
10.1177/10406387211027899 |
| Abstrakt: |
The immature platelet fraction (IPF) is a measure of newly released platelets, which has been used as a marker of platelet production in multiple human studies but is not widely available in multispecies analyzers. We developed gates to measure the IPF in diluted and undiluted murine blood samples on the Sysmex XN-1000V multispecies hematology analyzer. IPF gates were created using undiluted and diluted (1/10) blood samples obtained from adult and newborn (postnatal day 10, P10) C57BL/6J wild-type (WT) mice, and from 3 murine models of thrombocytopenia: c-MPL -/- mice, which lack the thrombopoietin receptor (hyporegenerative); antibody-mediated thrombocytopenia; and acute inflammation-induced thrombocytopenia. P10 mice were chosen because, at their size, we could consistently obtain (by terminal phlebotomy) the blood volume needed to run an undiluted sample. The undiluted blood IPF gate successfully differentiated between mechanisms of thrombocytopenia in both adult and P10 mice. For diluted samples, 2 IPF gates were generated: a thrombocytopenic (T) gate, which performed well in samples with platelet counts (PCs) <800 × 10 9 /L in adult mice and <500 × 10 9 /L in newborn mice, and a non-thrombocytopenic (NT) gate, which performed well in samples with PCs above these thresholds. PCs and IPFs measured in diluted blood using these gates agreed well with those measured in undiluted blood and had good reproducibility. These diluted gates allow for the accurate measurement of PCs and IPFs in small (10 µL) blood volumes, which can be obtained easily from adult and newborn mice as small as P1 to assess platelet production serially. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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