Extended storage and glucose exhaustion are associated with apoptotic changes in platelets stored in additive solution
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作者:
Johnson, Lacey
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Australian Red Cross Blood Serv, Res & Dev, Sydney, NSW, Australia
Canadian Blood Serv, Ctr Innovat, Vancouver, BC, Canada
Univ British Columbia, Ctr Blood Res, Vancouver, BC V5Z 1M9, CanadaAustralian Red Cross Blood Serv, Res & Dev, Sydney, NSW, Australia
Johnson, Lacey
[1
,2
,3
]
Schubert, Peter
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Canadian Blood Serv, Ctr Innovat, Vancouver, BC, Canada
Univ British Columbia, Ctr Blood Res, Vancouver, BC V5Z 1M9, CanadaAustralian Red Cross Blood Serv, Res & Dev, Sydney, NSW, Australia
Schubert, Peter
[2
,3
]
Tan, Shereen
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Australian Red Cross Blood Serv, Res & Dev, Sydney, NSW, AustraliaAustralian Red Cross Blood Serv, Res & Dev, Sydney, NSW, Australia
Tan, Shereen
[1
]
Devine, Dana V.
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Canadian Blood Serv, Ctr Innovat, Vancouver, BC, Canada
Univ British Columbia, Ctr Blood Res, Vancouver, BC V5Z 1M9, CanadaAustralian Red Cross Blood Serv, Res & Dev, Sydney, NSW, Australia
Devine, Dana V.
[2
,3
]
Marks, Denese C.
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Australian Red Cross Blood Serv, Res & Dev, Sydney, NSW, AustraliaAustralian Red Cross Blood Serv, Res & Dev, Sydney, NSW, Australia
Marks, Denese C.
[1
]
机构:
[1] Australian Red Cross Blood Serv, Res & Dev, Sydney, NSW, Australia
[2] Canadian Blood Serv, Ctr Innovat, Vancouver, BC, Canada
[3] Univ British Columbia, Ctr Blood Res, Vancouver, BC V5Z 1M9, Canada
BACKGROUNDThe storage of platelets (PLTs) in additive solution (AS) may facilitate improved PLT quality and possibly extension of the PLT shelf life. A minimum amount of plasma is required when PLTs are stored in AS, as a source of glucose. The aim of this study was to assess the effect of reducing the plasma carryover to 20% on PLT quality when stored in SSP+ for an extended period. STUDY DESIGN AND METHODSUsing a pool-and-split design, buffy coat-derived PLTs were stored in either 30% plasma/SSP+ or 20% plasma/SSP+. In vitro analyses were carried out to Day 10. Metabolites and markers of PLT activation and apoptosis were measured using a blood gas analyzer and flow cytometry. PLT apoptotic protein expression was investigated by Western blotting. RESULTSGlucose exhaustion occurred in the 20% plasma group between Day 7 and Day 10. The surface expression of P-selectin and PAC-1 was comparable on Day 10 in both groups, suggesting that the PLTs were not activated. However, the exposure of phosphatidylserine and the number of phosphatidylserine-positive microparticles were significantly higher in the 20% group on Day 10. The expression of the proapoptotic proteins Bak, Bax, and cleaved caspase-3 were higher in the 20% plasma group by Day 7 of storage, compared to the 30% plasma group. CONCLUSIONExhaustion of glucose was associated with a proapoptotic phenotype. Results such as these should be considered before extending the PLT shelf life beyond 7 days, particularly when stored in ASs lacking glucose with low plasma carryover.
机构:
US Army Inst Surg Res, Blood & Shock Resuscitat, Ft Sam Houston, TX USA
US Army Inst Surg Res, Blood & Shock Resuscitat, Ft Sam Houston, TX 78234 USAUS Army Inst Surg Res, Blood & Shock Resuscitat, Ft Sam Houston, TX USA
Reddoch-Cardenas, Kristin M.
McIntosh, Colby
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US Army Inst Surg Res, Blood & Shock Resuscitat, Ft Sam Houston, TX USAUS Army Inst Surg Res, Blood & Shock Resuscitat, Ft Sam Houston, TX USA
McIntosh, Colby
Barrera, Gema
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US Army Inst Surg Res, Blood & Shock Resuscitat, Ft Sam Houston, TX USAUS Army Inst Surg Res, Blood & Shock Resuscitat, Ft Sam Houston, TX USA
Barrera, Gema
Bynum, James A.
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UT Hlth San Antonio, San Antonio, TX USAUS Army Inst Surg Res, Blood & Shock Resuscitat, Ft Sam Houston, TX USA
机构:
Australian Red Cross Lifeblood, Res & Dev, Alexandria, NSW, Australia
Australian Red Cross Lifeblood, Res & Dev, 17 Riordan St, Alexandria, NSW 2015, AustraliaAustralian Red Cross Lifeblood, Res & Dev, Alexandria, NSW, Australia
Johnson, Lacey
Roan, Christopher
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Australian Red Cross Lifeblood, Res & Dev, Alexandria, NSW, AustraliaAustralian Red Cross Lifeblood, Res & Dev, Alexandria, NSW, Australia
Roan, Christopher
Lei, Pearl
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Australian Red Cross Lifeblood, Res & Dev, Alexandria, NSW, AustraliaAustralian Red Cross Lifeblood, Res & Dev, Alexandria, NSW, Australia
Lei, Pearl
Spinella, Philip C.
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Univ Pittsburgh Med Ctr, Trauma & Transfus Med Res Ctr, Dept Surg & Crit Care Med, Pittsburgh, PA USAAustralian Red Cross Lifeblood, Res & Dev, Alexandria, NSW, Australia
Spinella, Philip C.
Marks, Denese C.
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Australian Red Cross Lifeblood, Res & Dev, Alexandria, NSW, Australia
Univ Sydney, Sydney Med Sch, Camperdown, NSW, AustraliaAustralian Red Cross Lifeblood, Res & Dev, Alexandria, NSW, Australia