Abstract

Background Platelet-rich plasma (PRP) is a promising strategy for intervertebral disc degeneration. However, the potential harmful effects of leukocytes in PRP on nucleus pulposus-derived mesenchymal stem cells (NPMSCs) have seldom been studied. This study aimed at comparatively evaluating effects of pure platelet-rich plasma (P-PRP) and leukocyte-containing platelet-rich plasma (L-PRP) on rabbit NPMSCs in vitro. Methods NPMSCs isolated from rabbit NP tissues were treated with L-PRP or P-PRP in vitro, and then cell proliferation and expression of stem cell markers, proinflammatory cytokines (TNF-α, IL-1β), production of ECM (extracellular matrix-related protein), and NF-κB p65 protein were validated by CCK-8 assay, real-time polymerase chain reaction, enzyme-linked immunosorbent assay, immunofluorescence, and western blot respectively. Results NPMSCs differentiate into nucleus pulposus-like cells after treatment of PRPs (P-PRP and L-PRP), and NPMSCs exhibited maximum proliferation at a 10% PRP dose. L-PRP had observably higher concentration of leukocytes, TNF-α, and IL-1β than P-PRP. Furthermore, compared to P-PRP, L-PRP induced the differentiated NPMSCs to upregulate the expression of TNF-α and IL-1β, enhanced activation of the NF-κB pathway, increased the expression of MMP-1 and MMP-13, and produced less ECM in differentiated NPMSCs. Conclusions Both P-PRP and L-PRP can induce the proliferation and NP-differentiation of NPMSCs. Compared to L-PRP, P-PRP can avoid the activation of the NF-κB pathway, thus reducing the inflammatory and catabolic responses.

Highlights

  • As a major cause of low back pain, intervertebral disc degeneration (IDD) is drawing increasing attention for substantial financial and health care burdens worldwide [1]

  • The objective of this study is to comparatively evaluate effects of P-Platelet-rich plasma (PRP) and leukocyte-containing platelet-rich plasma (L-PRP) on rabbit nucleus pulposus-derived mesenchymal stem cells (NPMSCs) in vitro, and a new insight is provided to improve the efficiency of PRP treatment in disc regeneration

  • The expression of nucleus pulposus cell-related genes in the experimental groups was 3- to 4-folds higher than that in the control group (Figure 4(d)) there was no significant difference between pure platelet-rich plasma (P-PRP) groups and L-PRP groups (Figures 4(b)–4(d)). These results indicate that both L-PRP and P-PRP induced the differentiation of NPMSCs towards the mature NP-like cells

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Summary

Introduction

As a major cause of low back pain, intervertebral disc degeneration (IDD) is drawing increasing attention for substantial financial and health care burdens worldwide [1]. Conservative treatments, including oral analgesics and NSAIDs, are clinically applied to alleviate the symptoms [6]. Spinal surgeries, especially those with minimal invasive techniques, can efficiently relieve the symptoms of neural compression. Platelet-rich plasma (PRP) is a promising strategy for intervertebral disc degeneration. The potential harmful effects of leukocytes in PRP on nucleus pulposus-derived mesenchymal stem cells (NPMSCs) have seldom been studied. This study aimed at comparatively evaluating effects of pure platelet-rich plasma (P-PRP) and leukocyte-containing platelet-rich plasma (L-PRP) on rabbit NPMSCs in vitro. Compared to P-PRP, L-PRP induced the differentiated NPMSCs to upregulate the expression of TNF-α and IL-1β, enhanced activation of the NF-κB pathway, increased the expression of MMP-1 and MMP-13, and produced less ECM in differentiated NPMSCs. Conclusions. Compared to L-PRP, P-PRP can avoid the activation of the NF-κB pathway, reducing the inflammatory and catabolic responses

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