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将白细胞纳入富含血小板的血浆会降低支架的稳定性,并阻碍细胞外基质的重塑。

The inclusion of leukocytes into platelet rich plasma reduces scaffold stability and hinders extracellular matrix remodelling.

机构信息

BTI-Biotechnology Institute, Vitoria, Spain; University Institute for Regenerative Medicine & Oral Implantology, UIRMI (UPV/EHU-Fundación Eduardo Anitua), Vitoria, Spain.

BTI-Biotechnology Institute, Vitoria, Spain; University Institute for Regenerative Medicine & Oral Implantology, UIRMI (UPV/EHU-Fundación Eduardo Anitua), Vitoria, Spain.

出版信息

Ann Anat. 2022 Feb;240:151853. doi: 10.1016/j.aanat.2021.151853. Epub 2021 Nov 9.

Abstract

BACKGROUND

Scaffolds should have controllable degradation rate and allow cells to produce their own extracellular matrix. Platelet rich plasma (PRP) is a source of autologous growth factors and proteins embedded in a 3D fibrin scaffold. There is no consensus regarding the obtaining conditions and composition of PRPs. The aim of this study was to evaluate how the inclusion of leukocytes (L-PRP) in plasma rich in growth factors (PRGF) may alter the process of fibrinolysis. The effect of different combinations of cellular phenotypes with PRGF and L-PRP clots on both the fibrinolysis and matrix deposition process was also determined.

METHODS

PRGF and L-PRP clots were incubated for 14 days and D-dimer and type I collagen were determined in their conditioned media to evaluate clots' stability. For remodelling assays, gingival fibroblasts, alveolar osteoblasts and human umbilical vein endothelial cells (HUVEC) were seeded onto the two types of clots for 14 days. D-dimer, type I collagen, and laminin α4 were measured by ELISA kits in their conditioned media. Morphological and histological analysis were also performed. Cell proliferation was additionally determined RESULTS: PRGF clots preserved their stability as shown by the low levels of both D-dimer and collagen type I compared to those obtained for L-PRP clots. The inclusion of both gingival fibroblasts and alveolar osteoblasts stimulated a higher fibrinolysis in the PRGF clots. In contrast to this, the degradation rates of both PRGF and L-PRP clots remained unchanged after culturing with the endothelial cells. In all cases, type I collagen and laminin α4 levels were in line with the degree of clots' degradation. In all phenotypes, cell proliferation was significantly higher in PRGF than in L-PRP clots.

CONCLUSION

The inclusion of leukocytes in PRGF scaffolds reduced their stability, decreased cell number and slowed down cell remodelling.

摘要

背景

支架应具有可控制的降解速率,并允许细胞产生自己的细胞外基质。富含血小板的血浆(PRP)是自体生长因子和蛋白质的来源,嵌入在三维纤维蛋白支架中。关于 PRP 的获取条件和组成尚无共识。本研究旨在评估富含生长因子的血浆(PRGF)中白细胞(L-PRP)的包含如何改变纤维蛋白溶解过程。还确定了具有 PRGF 和 L-PRP 凝块的不同细胞表型组合对纤维蛋白溶解和基质沉积过程的影响。

方法

将 PRGF 和 L-PRP 凝块孵育 14 天,并在其条件培养基中测定 D-二聚体和 I 型胶原,以评估凝块的稳定性。对于重塑测定,将牙龈成纤维细胞、牙槽骨成骨细胞和人脐静脉内皮细胞(HUVEC)接种到两种类型的凝块上 14 天。通过 ELISA 试剂盒在其条件培养基中测定 D-二聚体、I 型胶原和层粘连蛋白α4。还进行了形态学和组织学分析。此外,还测定了细胞增殖。

结果

PRGF 凝块保持了其稳定性,与 L-PRP 凝块相比,D-二聚体和 I 型胶原的水平均较低。同时包含牙龈成纤维细胞和牙槽骨成骨细胞可刺激 PRGF 凝块中更高的纤维蛋白溶解。与此相反,在用内皮细胞培养后,PRGF 和 L-PRP 凝块的降解率保持不变。在所有情况下,I 型胶原和层粘连蛋白α4 的水平均与凝块降解的程度一致。在所有表型中,PRGF 凝块中的细胞增殖均明显高于 L-PRP 凝块。

结论

白细胞包含在 PRGF 支架中降低了其稳定性,减少了细胞数量并减缓了细胞重塑。

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