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[Effects of Platelet-Rich Plasma on Macrophage Phenotype and Its Influencing Factors].
Liu, Yu-Lin; Wang, De-Qing; Xiao, Pan; Guo, Han; Huang, Yuan-Shuai; Zhuang, Yuan.
Afiliación
  • Liu YL; Department of Blood Transfusion, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, Sichuan Province, China.
  • Wang DQ; Department of Blood Transfusion Medicine, The First Medical Center of Chinese PLA General Hospital, Beijing 100853, China.
  • Xiao P; Department of Blood Transfusion, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, Sichuan Province, China.
  • Guo H; State Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China,University of Chinese Academy of Sciences, Beijing 100049, China.
  • Huang YS; Department of Blood Transfusion, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, Sichuan Province, China,E-mail: hys@live.cn.
  • Zhuang Y; Department of Blood Transfusion Medicine, The First Medical Center of Chinese PLA General Hospital, Beijing 100853, China,E-mail: zhuangyuan0215@126.com.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 31(4): 1155-1163, 2023.
Article en Zh | MEDLINE | ID: mdl-37551492
ABSTRACT

OBJECTIVE:

To evaluate the effects of platelet-rich plasma (PRP) supernatants with different activation methods and storage time on human monocyte-derived macrophages phenotype and explore the possible mechanism.

METHODS:

Human monocyte-derived macrophages were cultured in vitro with PRP or activated PRP supernatants activated with different activators. The expression of marker molecules on the surface of macrophages was detected by flow cytometry, and the concentration of growth factors in PRP supernatants was detected by ELISA.

RESULTS:

After 24 h of coculture, the expression level of CD86 in macrophages stimulated by PRP supernatant (thrombin and Cacl2 activated) was significantly higher than that by PRP group (P<0.05), and the expression of CD163 in macrophages was increased by Cacl2 activated PRP supernatant. Compared with different activator groups, the expression of CD163 in macrophages of Cacl2 activated group was significantly higher than that of thrombin and ADP groups (P<0.05). ELISA results showed that the concentrations of FGF (P<0.001) and EGF (P<0.05) in the supernatant of PRP stored at -80 ℃ for more than 20 months and 10-20 months were significantly higher than those in the group stored at less than 10 months after Cacl2 activation, and the expressions of CD86 (P<0.01), CD163 (P<0.001) and CD206 (P<0.001) in macrophages cocultured with the supernatant of the two groups were significantly increased.

CONCLUSION:

PRP activated by different activators has different effects on the phenotype of macrophages. Meanwhile, the storage time will also affect the growth factor concentration and effect of PRP.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Asunto de la revista: HEMATOLOGIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Asunto de la revista: HEMATOLOGIA Año: 2023 Tipo del documento: Article