The phenotype of cryopreserved platelets influences the formation of platelet-leukocyte aggregates in an in vitro model
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Winskel-Wood, Ben
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Australian Red Cross Lifeblood, Res & Dev, Sydney, NSW, Australia
Univ Technol Sydney, Sch Life Sci, Sydney, NSW, AustraliaAustralian Red Cross Lifeblood, Res & Dev, Sydney, NSW, Australia
Winskel-Wood, Ben
[1
,2
]
Padula, Matthew P.
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Univ Technol Sydney, Sch Life Sci, Sydney, NSW, AustraliaAustralian Red Cross Lifeblood, Res & Dev, Sydney, NSW, Australia
Padula, Matthew P.
[2
]
Marks, Denese C.
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Australian Red Cross Lifeblood, Res & Dev, Sydney, NSW, Australia
Univ Sydney, Sydney Med Sch, Sydney, NSW, AustraliaAustralian Red Cross Lifeblood, Res & Dev, Sydney, NSW, Australia
Marks, Denese C.
[1
,3
]
Johnson, Lacey
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Australian Red Cross Lifeblood, Res & Dev, Sydney, NSW, Australia
Univ Technol Sydney, Sch Life Sci, Sydney, NSW, Australia
Australian Red Cross Lifeblood, Res & Dev, 17 ORiordan St, Alexandria, NSW 2015, AustraliaAustralian Red Cross Lifeblood, Res & Dev, Sydney, NSW, Australia
Johnson, Lacey
[1
,2
,4
]
机构:
[1] Australian Red Cross Lifeblood, Res & Dev, Sydney, NSW, Australia
[2] Univ Technol Sydney, Sch Life Sci, Sydney, NSW, Australia
[3] Univ Sydney, Sydney Med Sch, Sydney, NSW, Australia
[4] Australian Red Cross Lifeblood, Res & Dev, 17 ORiordan St, Alexandria, NSW 2015, Australia
Cryopreservation significantly alters the phenotype of platelets; generating distinct subpopulations, which may influence the formation of platelet leukocyte aggregates (PLA). PLAs are immunomodulatory and have been associated with transfusion-associated adverse events. As such, the aim of this study was to examine the effect of cryopreservation on the ability of platelets to form PLAs, using a monocyte-like cell line (THP-1). Platelets were tested pre-freeze, post-thaw and following stimulation with TRAP-6 or A23187, both alone and following co-culture with THP-1 cells for 1 and 24 hours (n = 6). Platelet subpopulations and platelet-THP-1 cell aggregates were analyzed using multi-color imaging flow cytometry using Apotracker Green (ApoT), CD42b, CD62P, CD61, and CD45. Cryopreservation resulted in the generation of activated (ApoT-/CD42b+/CD62P+), procoagulant (ApoT+/CD42b+/CD62P+) and a novel (ApoT+/CD42b+/CD62P-) platelet subpopulation. Co-incubation of cryopreserved platelets with THP-1 cells increased PLA formation compared to pre-freeze but not TRAP-6 or A23187 stimulated platelets. P-selectin on the surface membrane was correlated with increased PLA formation. Our findings demonstrate that cryopreservation increases the interaction between platelets and THP-1 cells, largely due to an increase in procoagulant platelets. Further investigation is required to determine the immunological consequences of this interaction. Plain Language Summary What do we know? Cryopreserved platelets are an alternative to overcome issues with the short shelf-life of room-temperature stored platelets After thawing, cryopreserved platelets exhibit changes in cell structure and receptor abundance Activated platelets can attach to leukocytes, forming platelet-leukocyte aggregates and altering their immune function Platelet-leukocyte aggregates can increase inflammation, which is associated with adverse events after transfusion, which can negatively affect patient outcomes What did we discover? Cryopreservation results in a heterogenous mix of platelet subpopulations Cryopreserved platelets display increased adherence to a monocyte-like cell line (THP-1 cells). Platelet-THP-1 aggregate formation was linked to expression of CD62P on the surface of the platelets The increase in cryopreserved platelet-THP-1 cell aggregates was largely due to an increase in procoagulant platelets What is the impact? Our data demonstrate that cryopreservation increases platelet interaction with a monocyte-like cell line This may mediate immune responses and/or circulation time of transfused platelets
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Sichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R ChinaSichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R China
Yang, Shenghan
Huang, Xunbei
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Sichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R ChinaSichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R China
Huang, Xunbei
Liao, Juan
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Sichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R ChinaSichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R China
Liao, Juan
Li, Qin
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Sichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R ChinaSichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R China
Li, Qin
Chen, Si
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Sichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R ChinaSichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R China
Chen, Si
Liu, Chaonan
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Sichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R ChinaSichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R China
Liu, Chaonan
Ling, Liqin
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Sichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R ChinaSichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R China
Ling, Liqin
Zhou, Jing
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Sichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R ChinaSichuan Univ, West China Hosp, Dept Lab Med, 37,Guoxuexiang, Chengdu 610041, Peoples R China