Red blood cell–derived microparticles isolated from blood units initiate and propagate thrombin generation. Issue 8 (11th December 2012)
- Record Type:
- Journal Article
- Title:
- Red blood cell–derived microparticles isolated from blood units initiate and propagate thrombin generation. Issue 8 (11th December 2012)
- Main Title:
- Red blood cell–derived microparticles isolated from blood units initiate and propagate thrombin generation
- Authors:
- Rubin, Olivier
Delobel, Julien
Prudent, Michel
Lion, Niels
Kohl, Kid
Tucker, Erik I.
Tissot, Jean‐Daniel
Angelillo‐Scherrer, Anne - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="trf12008-sec-0001" sec-type="section"> <title>Background</title> <p>Red blood cell–derived microparticles (RMPs) are small phospholipid vesicles shed from RBCs in blood units, where they accumulate during storage. Because microparticles are bioactive, it could be suggested that RMPs are mediators of posttransfusion complications or, on the contrary, constitute a potential hemostatic agent.</p> </sec> <sec id="trf12008-sec-0002" sec-type="section"> <title>Study Design and Methods</title> <p>This study was performed to establish the impact on coagulation of RMPs isolated from blood units. Using calibrated automated thrombography, we investigated whether RMPs affect thrombin generation (TG) in plasma.</p> </sec> <sec id="trf12008-sec-0003" sec-type="section"> <title>Results</title> <p>We found that RMPs were not only able to increase TG in plasma in the presence of a low exogenous tissue factor (TF) concentration, but also to initiate TG in plasma in absence of exogenous TF. TG induced by RMPs in the absence of exogenous TF was neither affected by the presence of blocking anti‐TF nor by the absence of Factor (F)VII. It was significantly reduced in plasma deficient in FVIII or F IX and abolished in FII‐, FV‐, FX‐, or FXI‐deficient plasma. TG was also totally abolished when anti‐XI 01A6 was added in the sample. Finally, neither Western blotting, flow cytometry, nor immunogold labeling<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="trf12008-sec-0001" sec-type="section"> <title>Background</title> <p>Red blood cell–derived microparticles (RMPs) are small phospholipid vesicles shed from RBCs in blood units, where they accumulate during storage. Because microparticles are bioactive, it could be suggested that RMPs are mediators of posttransfusion complications or, on the contrary, constitute a potential hemostatic agent.</p> </sec> <sec id="trf12008-sec-0002" sec-type="section"> <title>Study Design and Methods</title> <p>This study was performed to establish the impact on coagulation of RMPs isolated from blood units. Using calibrated automated thrombography, we investigated whether RMPs affect thrombin generation (TG) in plasma.</p> </sec> <sec id="trf12008-sec-0003" sec-type="section"> <title>Results</title> <p>We found that RMPs were not only able to increase TG in plasma in the presence of a low exogenous tissue factor (TF) concentration, but also to initiate TG in plasma in absence of exogenous TF. TG induced by RMPs in the absence of exogenous TF was neither affected by the presence of blocking anti‐TF nor by the absence of Factor (F)VII. It was significantly reduced in plasma deficient in FVIII or F IX and abolished in FII‐, FV‐, FX‐, or FXI‐deficient plasma. TG was also totally abolished when anti‐XI 01A6 was added in the sample. Finally, neither Western blotting, flow cytometry, nor immunogold labeling allowed the detection of traces of TF antigen. In addition, RMPs did not comprise polyphosphate, an important modulator of coagulation.</p> </sec> <sec id="trf12008-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Taken together, our data show that RMPs have FXI‐dependent procoagulant properties and are able to initiate and propagate TG. The anionic surface of RMPs might be the site of FXI‐mediated TG amplification and intrinsic tenase and prothrombinase complex assembly.</p> </sec> </abstract> … (more)
- Is Part Of:
- Transfusion. Volume 53:Issue 8(2013)
- Journal:
- Transfusion
- Issue:
- Volume 53:Issue 8(2013)
- Issue Display:
- Volume 53, Issue 8 (2013)
- Year:
- 2013
- Volume:
- 53
- Issue:
- 8
- Issue Sort Value:
- 2013-0053-0008-0000
- Page Start:
- 1744
- Page End:
- 1754
- Publication Date:
- 2012-12-11
- Subjects:
- Hematology -- Periodicals
Blood -- Transfusion -- Periodicals
Blood Group Antigens -- Periodicals
Blood Preservation -- Periodicals
Blood Transfusion -- Periodicals
615 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1537-2995 ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=trf ↗
http://www.transfusion.org ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/trf.12008 ↗
- Languages:
- English
- ISSNs:
- 0041-1132
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9020.704000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3966.xml