Chinese Journal of Tissue Engineering Research ›› 2013, Vol. 17 ›› Issue (16): 2981-2988.doi: 10.3969/j.issn.2095-4344.2013.16.019

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Inflammatory factor release from leukocyte- and platelet-rich plasma gel

Wen Tian-yang1, Wang Ai-hong2, Xu Zhang-rong2   

  1. 1 Department of Endocrinology, the 306th Teaching Hospital of PLA, Peking University, Beijing  100101, China
    2 Department of Endocrinology, Diabetes Center, the 306th Hospital of PLA, Beijing  100101, China
  • Received:2013-02-04 Revised:2013-03-26 Online:2013-04-16 Published:2013-04-16
  • Contact: Xu Zhang-rong, Master, Chief physician, Department of Endocrinology, Diabetes Center, the 306th Hospital of PLA, Beijing 100101, China xzr1021@vip.sina.com
  • About author:Wen Tian-yang★, Studying for master’s degree, Department of Endocrinology, the 306th Teaching Hospital of PLA, Peking University, Beijing 100101, China pekingkw@163.com
  • Supported by:

    the Military Clinical High and New Technology in 2010, No. 2010gxjs054*

Abstract:

BACKGROUND: Current studies about leukocyte- and platelet-rich plasma gel mainly focus on growth factor release and the mechanism underlying promoting tissue growth and wound healing.
OBJECTIVE: To investigate the mechanism of leukocyte- and platelet-rich plasma gel by measuring the levels of interleukin-1, interleukin-4, interleukin-6, platelet-derived growth factor-BB, transforming growth factor-β1, and vascular endothelial growth factor released from leukocyte- and platelet-rich plasma gel and observing the ultrastructure of leukocyte- and platelet-rich plasma gel.
METHODS: Blood samples were collected from 12 healthy volunteers. Leukocyte- and platelet-rich plasma was produced by two-step centrifugation, and leukocyte- and platelet-rich plasma gel was obtained by combining the leukocyte- and platelet-rich plasma with thrombin and calcium gluconate (10:1). The leukocyte- and platelet-rich plasma gel was preserved in Dulbecco’s modified Eagle’s medium, and the Dulbecco’s modified Eagle’s medium including exudates of leukocyte- and platelet-rich plasma gel was collected at days 1, 3, 7, 14, 21.
RESULTS AND CONCLUSION: Enzyme linked immunoabsorbent assay showed that the leukocyte formula in the leukocyte- and platelet-rich plasma gel was different from that in the whole blood, and lymphocytes shared the largest proportion. Interleukin-1 level peaked at 0-1 day of culture (P < 0.05), and then gradually decreased. Interleukin-4 level showed no changes at different periods. Interleukin-6 maintained a higher release at 0-1, 2-3, and 4-7 days, but dramatically reduced at 8-14 and 15-21 days of culture (P < 0.05). The release amount of platelet-derived growth factor-BB, transforming growth factor-β1 reached the peak at 1 day of culture (P < 0.05), and then exhibited a raped decline. The release amount of vascular endothelial growth factor gradually increased at 7 days of culture, and then gradually declined at 8-21 days of culture. Under the scanning electron microscope, vast majority of leukocytes in the leukocyte- and platelet-rich plasma gel were confirmed as lymphocytes. Results showed that besides the expression of growth factors such as platelet-derived growth factor-BB, transforming growth factor-β1, and vascular endothelial growth factor, the concentrations and components change of lymphocytes and expression of inflammatory factors such as interleukin-1, interleukin-4, and interleukin-6 might be one of the mechanisms by which leukocyte- and platelet-rich plasma gel can promote wound healing.

Key words: biomaterials, extracellular matrix materials, leukocyte-and platelet-rich plasma, gel, leukocytes, inflammatory factors, other grants-supported paper

CLC Number: