凝血酶在富血小板血浆(PRP)制备中的作用的体外研究:凝胶形成的效用和生长因子释放的影响。

IF 1.1 Q4 CELL & TISSUE ENGINEERING Journal of Stem Cells & Regenerative Medicine Pub Date : 2016-05-30 eCollection Date: 2016-01-01
Stephany Cares Huber, José Luiz Rosenberis Cunha Júnior, Silmara Montalvão, Letícia Queiroz da Silva, Aline Urban Paffaro, Francesca Aparecida Ramos da Silva, Bruno Lima Rodrigues, José Fabio Santos Duarte Lana, Joyce Maria Annichino-Bizzacchi
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引用次数: 0

摘要

简介:PRP的应用已在不同领域得到研究,在再生医学方面取得了可喜的成果。到目前为止,文献中还没有评价血清凝血酶水平的研究,并将其作为自体凝血酶制剂。因此,在本研究中,我们评估了不同凝血酶浓度在PRP中的作用以及对生长因子释放的影响。同时,对不同的PRP凝胶形成活化剂进行了评价。方法:测定不同自体制剂中的凝血酶水平:血清、L-PRP(富含白细胞的PRP)和T-PRP(通过PRP添加葡萄糖酸钙产生的凝血酶)。根据文献制备L-PRP,并对血小板和白细胞进行定量。通过测定凝血酶凝胶形成时间,观察与钙不相关的自体凝血酶对PRP凝胶的影响。通过生长因子(PDGF-AA、VEGF和EGF)多重分析确定凝血酶浓度与生长因子释放的关系。结果:血清凝血酶、L-PRP和T-PRP浓度相近(分别为8.13 nM、8.63 nM和7.56 nM),个体间差异较大(CV%分别为35.07、43和58.42)。T-PRP与含氯化钙的血清在促进凝胶形成的时间上表现出相似的结果。凝血酶浓度(2.66、8和24 nM)的增加没有促进生长因子释放的增加。结论:以血清作为凝血酶源的技术是促进PRP凝胶形成的最有效和可重复性的技术,与其他激活方法相比具有一定的优势,因为该技术更简单,更快,不需要消耗部分PRP。值得注意的是,使用不同凝血酶浓度激活PRP并没有促进生长因子的更高释放,当PRP作为混悬液使用时,似乎没有必要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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In vitro study of the role of thrombin in platelet rich plasma (PRP) preparation: utility for gel formation and impact in growth factors release.

Introduction: The use of PRP has been studied for different fields, with promising results in regenerative medicine. Until now, there is no study in the literature evaluating thrombin levels in serum, used as autologous thrombin preparation. Therefore, in the present study we evaluated the role played by different thrombin concentrations in PRP and the impact in the release of growth factors. Also, different activators for PRP gel formation were evaluated.

Methods: Thrombin levels were measured in different autologous preparations: serum, L-PRP (PRP rich in leukocytes) and T-PRP (thrombin produced through PRP added calcium gluconate). L-PRP was prepared according to the literature, with platelets and leukocytes being quantified. The effect of autologous thrombin associated or not with calcium in PRP gel was determined by measuring the time of gel formation. The relationship between thrombin concentration and release of growth factors was determined by growth factors (PDGF-AA, VEGF and EGF) multiplex analysis.

Results: A similar concentration of thrombin was observed in serum, L-PRP and T-PRP (8.13 nM, 8.63 nM and 7.56 nM, respectively) with a high variation between individuals (CV%: 35.07, 43 and 58.42, respectively). T-PRP and serum with calcium chloride showed similar results in time to promote gel formation. The increase of thrombin concentrations (2.66, 8 and 24 nM) did not promote an increase in growth factor release.

Conclusions: The technique of using serum as a thrombin source proved to be the most efficient and reproducible for promoting PRP gel formation, with some advantages when compared to other activation methods, as this technique is easier and quicker with no need of consuming part of PRP. Noteworthy, PRP activation using different thrombin concentrations did not promote a higher release of growth factors, appearing not to be necessary when PRP is used as a suspension.

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来源期刊
CiteScore
3.40
自引率
0.00%
发文量
5
审稿时长
14 weeks
期刊最新文献
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