Center for Tissue Engineering, Department of Plastic Surgery, University of California, Orange, CA.
Center for Tissue Engineering, Department of Plastic Surgery, University of California, Orange, CA.
J Hand Surg Am. 2023 Sep;48(9):914-922. doi: 10.1016/j.jhsa.2023.06.007. Epub 2023 Jul 20.
Currently, no treatment corrects the contractile nature of Dupuytren myofibroblasts (DMFs) or prevents recurrence following surgery. Antifibrotic and proadipogenic growth factors are released when adipose-derived stem cells (ASCs) are cultured with platelet-rich plasma (PRP), a platelet concentration from whole blood. Reprograming myofibroblasts into adipocytes via growth factors is proposed as a powerful potential tool to target fibrosis. We aimed to assess whether the combination of ASCs and PRP reprograms DMFs into adipocytes in vitro and alters their contractile nature in vivo.
Normal human dermal fibroblasts (NHDFs) and DMFs from Dupuytren patients were isolated and cocultured with ASCs and PRP either alone or together. Adipocytes were detected by Oil Red O and perilipin staining. DMFs and NHDFs were transplanted into the forepaws of rats (Rowett Nude [rnu/rnu]) and treated with saline, PRP+ASCs, or collagenase Clostridium histolyticum (clinical comparison) 2 months later. After 2 weeks, the tissue was harvested and subjected to Masson trichrome staining, and collagen I and III and alpha-smooth muscle actin detection by immunohistochemistry.
Myofibroblasts transform into adipocytes upon coculture with PRP+ASCs. DMFs show increased alpha-smooth muscle actin expression in vivo compared with NHDFs, which is significantly decreased after PRP+ASCs and collagenase Clostridium histolyticum treatments. DMFs induce collagen I and III expressions in rat paws compared with NHDFs, with a type III to I ratio increase. Treatment with PRP+ASC reduced the ratio, but collagenase Clostridium histolyticum did not.
Treating DMFs with PRP+ASCs provides factors that induce myofibroblast to adipocyte transformation. This treatment reduces the contractile phenotype and fibrosis markers in vivo. Future studies should detail the mechanism of this conversion.
The combination of PRP and ASCs to induce the differentiation of DMFs into adipocytes may serve to limit surgery to a percutaneous contracture release and biological injection, rather than a moderate or radical fasciectomy, and reduce the recurrence of Dupuytren contracture.
目前,尚无治疗方法可纠正迪普屈恩肌成纤维细胞(DMF)的收缩性质,也无法防止手术后复发。当脂肪来源的干细胞(ASC)与富含血小板的血浆(PRP)(全血中的血小板浓度)一起培养时,会释放出抗纤维化和促脂肪生成的生长因子。通过生长因子将肌成纤维细胞重编程为脂肪细胞被提议作为一种强大的潜在工具来靶向纤维化。我们旨在评估 ASC 和 PRP 的组合是否可在体外将 DMF 重编程为脂肪细胞,并改变其体内的收缩性质。
分离正常的人真皮成纤维细胞(NHDF)和来自迪普屈恩患者的 DMF,并将其与 ASC 和 PRP 单独或一起共培养。通过油红 O 和 perilipin 染色检测脂肪细胞。将 DMF 和 NHDF 移植到罗特内德裸鼠(rnu/rnu)的前爪中,并在 2 个月后用生理盐水、PRP+ASC 或胶原酶 Clostridium histolyticum(临床比较)进行治疗。2 周后,采集组织进行 Masson 三色染色,并通过免疫组织化学检测胶原 I 和 III 以及 alpha-平滑肌肌动蛋白的表达。
在与 PRP+ASC 共培养时,肌成纤维细胞转化为脂肪细胞。与 NHDF 相比,DMF 在体内显示出更高的 alpha-平滑肌肌动蛋白表达,经 PRP+ASC 和胶原酶 Clostridium histolyticum 治疗后明显降低。与 NHDF 相比,DMF 可诱导大鼠爪子中的胶原 I 和 III 表达,并增加 III 型到 I 型的比值。PRP+ASC 治疗可降低该比值,但胶原酶 Clostridium histolyticum 则不能。
用 PRP+ASC 治疗 DMF 可提供诱导肌成纤维细胞向脂肪细胞转化的因子。这种治疗可减少体内的收缩表型和纤维化标志物。未来的研究应详细阐明这种转化的机制。
PRP 和 ASC 的组合诱导 DMF 分化为脂肪细胞,可能有助于将手术限制为经皮挛缩松解和生物注射,而不是中度或根治性筋膜切开术,并降低迪普屈恩挛缩的复发率。