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定制的富含血小板血浆与转化生长因子β1中和抗体以减少骨骼肌纤维化。

Customized platelet-rich plasma with transforming growth factor β1 neutralization antibody to reduce fibrosis in skeletal muscle.

作者信息

Li Hongshuai, Hicks Justin J, Wang Ling, Oyster Nick, Philippon Marc J, Hurwitz Shepard, Hogan MaCalus V, Huard Johnny

机构信息

Musculoskeletal Growth & Regeneration Laboratory, Department of Orthopaedic Surgery, University of Pittsburgh, Pittsburgh, PA 15219, USA.

Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA 15219, USA.

出版信息

Biomaterials. 2016 May;87:147-156. doi: 10.1016/j.biomaterials.2016.02.017. Epub 2016 Feb 17.

Abstract

UNLABELLED

The formation of fibrous tissue during the healing of skeletal muscle injuries leads to incomplete recovery of the injured muscle. Platelet-rich-plasma (PRP) contains beneficial growth factors for skeletal muscle repair; however, it also contains deleterious cytokines and growth factors, such as TGF-β1, that can cause fibrosis and inhibit optimal muscle healing.

OBJECTIVE

To test if neutralizing TGF-β1's action within PRP, through neutralization antibodies, could improve PRP's beneficial effect on skeletal muscle repair.

METHODS

PRP was isolated from in-bred Fisher rats. TGF-β1 neutralization antibody (Ab) was used to block the TGF-β1 within the PRP prior to injection. The effects of customized PRP (TGF-β1 neutralized PRP) on muscle healing was tested on a cardiotoxin (CTX) induced muscle injury model.

RESULTS

A significant increase in the numbers of regenerative myofibers was observed in the PRP and customized PRP groups compared to the untreated control. A significant decrease in collagen deposition was observed in customized PRP groups when compared to the control and PRP groups. Significantly enhanced angiogenesis and more Pax-7 positive satellite cells were found in the PRP and customized PRP groups compared to the control group. Macrophage infiltration was increased in the customized PRP groups when compared with the PRP group. More M2 macrophages were recruited to the injury site in the customized PRP groups when compared with the PRP and control groups.

CONCLUSION

Neutralizing TGF-β1 within PRP significantly promotes muscle regeneration while significantly reducing fibrosis. Not only did the neutralization reduce fibrosis, it enhanced angiogenesis, prolonged satellite cell activation, and recruited a greater number of M2 macrophages to the injury site which also contributed to the efficacy that the customized PRP had on muscle healing.

摘要

未标记

骨骼肌损伤愈合过程中纤维组织的形成会导致受损肌肉无法完全恢复。富血小板血浆(PRP)含有对骨骼肌修复有益的生长因子;然而,它也含有有害的细胞因子和生长因子,如转化生长因子-β1(TGF-β1),可导致纤维化并抑制肌肉的最佳愈合。

目的

通过中和抗体测试在PRP中中和TGF-β1的作用是否能改善PRP对骨骼肌修复的有益作用。

方法

从近交系Fisher大鼠中分离PRP。在注射前,使用TGF-β1中和抗体(Ab)阻断PRP中的TGF-β1。在心脏毒素(CTX)诱导的肌肉损伤模型上测试定制PRP(TGF-β1中和PRP)对肌肉愈合的影响。

结果

与未治疗的对照组相比,PRP组和定制PRP组中再生肌纤维数量显著增加。与对照组和PRP组相比,定制PRP组中胶原沉积显著减少。与对照组相比,PRP组和定制PRP组中血管生成显著增强,Pax-7阳性卫星细胞更多。与PRP组相比,定制PRP组中巨噬细胞浸润增加。与PRP组和对照组相比,定制PRP组中有更多的M2巨噬细胞被募集到损伤部位。

结论

中和PRP中的TGF-β1可显著促进肌肉再生,同时显著减少纤维化。中和不仅减少了纤维化,还增强了血管生成,延长了卫星细胞的激活,并将更多的M2巨噬细胞募集到损伤部位,这也有助于定制PRP对肌肉愈合的疗效。

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