Is exclusion of leukocytes from platelet-rich plasma (PRP) a better choice for early intervertebral disc regeneration?

被引:30
|
作者
Wang, Shan-zheng [1 ,2 ]
Fan, Wei-min [1 ]
Jia, Jun [2 ]
Ma, Liang-yu [2 ]
Yu, Jia-bin [2 ]
Wang, Chen [2 ]
机构
[1] Nanjing Med Univ, Clin Sch 1, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Southeast Univ, Med Sch, Zhongda Hosp, Dept Orthopaed, 87 Ding Jia Qiao Rd, Nanjing 210009, Jiangsu, Peoples R China
来源
STEM CELL RESEARCH & THERAPY | 2018年 / 9卷
基金
中国国家自然科学基金;
关键词
Platelet-rich plasma; Leukocyte; and platelet-rich plasma; Pure platelet-rich plasma; Intervertebral disc degeneration; Nucleus pulposus; Stem cells; LOW-BACK-PAIN; MOLECULAR THERAPY; DEGENERATION; CELLS; DISKECTOMY; INJECTION;
D O I
10.1186/s13287-018-0937-7
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background: Platelet-rich plasma (PRP) is becoming a promising strategy to treat early intervertebral disc degeneration (IDD) in clinics. Pure PRP without leukocytes (P-PRP) may decrease the catabolic and inflammatory changes in the early degenerated intervertebral discs. The aim of this study was to investigate the effects of P-PRP on nucleus pulposus-derived stem cells (NPSCs) isolated from early degenerated intervertebral discs in vitro. Methods: NPSCs isolated from early degenerated discs of rabbits were treated with P-PRP or leukocyte-platelet-rich PRP (L-PRP) in vitro, followed by measuring cell proliferation, stem cell marker expression, inflammatory gene expression, and anabolic and catabolic protein expression by immunostaining, quantitative real-time polymerase chain reaction, Western blot, and enzyme-linked immunosorbent assay. Results: Cell proliferation was induced by P-PRP in a dose-dependent manner with maximum proliferation at 10% P-PRP dose. P-PRP induced differentiation of NPSCs into active nucleus pulposus cells. P-PRP mainly increased the expression of anabolic genes and relative proteins, aggrecan (AGC), collagen types II (Col II), while L-PRP predominantly increased the expression of catabolic and inflammatory genes, matrix metalloproteinase-1 (MMP-1), MMP-13, interleukin-1 beta (IL-1 beta), IL-6, tumor necrosis factor alpha (TNF-alpha), and protein production of IL-1 beta and TNF-alpha. Conclusions: Leukocytes in PRP activate inflammatory and catabolic effects on NPSCs from early degenerated intervertebral discs. Hence, P-PRP may be a more suitable therapeutic strategy for early IDD.
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页数:11
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