Leukocyte-Rich Platelet-Rich Plasma Has Better Stimulating Effects on Tenocyte Proliferation Compared With Leukocyte-Poor Platelet-Rich Plasma

被引:23
作者
Lin, Keng-Yi [1 ,4 ]
Chen, Poyu [1 ,5 ,6 ]
Chen, Alvin Chao-Yu [1 ,2 ,7 ,8 ]
Chan, Yi-Sheng [1 ,2 ,7 ,8 ]
Lei, Kin Fong [1 ,3 ]
Chiu, Chih-Hao [1 ,2 ,8 ,9 ]
机构
[1] Chang Gung Univ, Taoyuan, Taiwan
[2] Chang Gung Mem Hosp, Dept Orthoped Surg, 123 Dinghu Rd, Taoyuan 333, Taiwan
[3] Chang Gung Univ, Grad Inst Biomed Engn, 259 Wen Hwa 1st Rd, Taoyuan 333, Taiwan
[4] Chang Gung Univ, Dept Med, Taoyuan, Taiwan
[5] Chang Gung Univ, Dept Occupat Therapy, Coll Med, Taoyuan, Taiwan
[6] Chang Gung Univ, Grad Inst Behav Sci, Coll Med, Taoyuan, Taiwan
[7] Chang Gung Mem Hosp, Dept Orthoped Surg, Linkou, Taiwan
[8] Chang Gung Mem Hosp, Bone & Joint Res Ctr, Linkou, Taiwan
[9] Chang Gung Mem Hosp, Comprehens Sports Med Ctr, Taoyuan, Taiwan
关键词
rotator cuff; tenocytes; platelet-rich plasma; leukocyte; ROTATOR CUFF; FIBRIN MATRIX; INTRATENDON DELIVERY; TENDON REPAIR; METABOLISM; TGF-BETA-1; INJURY; CELLS; BONE;
D O I
10.1177/23259671221084706
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Rotator cuff (RC) tendinopathy is one of the most common causes of shoulder pain. Platelet-rich plasma (PRP) has been frequently used in clinical scenarios, but its efficacy remains inconsistent. Purpose: To investigate the different responses of human tenocytes from torn RCs to leukocyte-rich PRP (LR-PRP) and leukocyte-poor PRP (LP-PRP) in a 2-chamber coculture device. Study Design: Controlled laboratory study. Methods: PRP was prepared using different platelet and leukocyte concentrations according to 5 groups: (1) LR-PRP with 5000 platelets/mu L, (2) LR-PRP with 10,000 platelets/mu L, (3) LP-PRP with 5000 platelets/mu L, (4) LP-PRP with 10,000 platelets/mu L, and (5) control with only culture medium supplementation and without PRP stimulation. Platelet-derived growth factor-AB (PDGF-AB) and transforming growth factor-beta 1 (TGF-beta 1) were measured in LR-PRP and LP-PRP via enzyme-linked immunosorbent assay. Microscopy, water-soluble tetrazolium salt assay, and quantitative real-time polymerase chain reaction were used to investigate the morphology, proliferation, and gene expression of RC tenocytes exposed to different PRP formulations. Data were collected from at least 3 independent measurements. The results were analyzed via 1-way analysis of variance, followed by the post hoc Bonferroni test. Results: The ratio of leukocytes to 5000 platelets/mu L was 29.5 times higher in LR-PRP than in LP-PRP (P < .05). In the 5000 platelets/mu L groups, the levels of TGF-beta 1 and PDGF-AB were both significantly higher in LR-PRP versus LP-PRP (TGF-beta 1: 367.0 +/- 16.5 vs 308.6 +/- 30.3 pg/mL, respectively [P = .043]; PDGF-AB: 172.1 +/- 1.8 vs 94.1 +/- 4.2 pg/mL, respectively [P < .001]). Compared with the control group, RC tenocyte proliferation was 1.42 +/- 0.01 and 1.41 +/- 0.03 times higher in the LR-PRP groups with 5000 platelets/mu L and 10,000 platelets/mu L, respectively (P < .05). The expression of tenocyte-related genes was higher in tenocytes cultured in LR-PRP. Conclusion: Both the LR-PRP groups with 5000 platelets/mu L and 10,000 platelets/mu L induced more growth factor release and increased RC tenocyte proliferation than did the LP-PRP groups.
引用
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页数:8
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