Tissue Engineering Centre, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Yaccob Latif, Cheras 56000, Kuala Lumpur, Malaysia.
Ear Nose & Throat Consultant Clinic, Ampang Puteri Specialist Hospital, 1 Jalan Mamanda 9, Ampang 68000, Selangor, Malaysia.
Int J Mol Sci. 2020 Apr 22;21(8):2929. doi: 10.3390/ijms21082929.
Fibroblasts secrete many essential factors that can be collected from fibroblast culture medium, which is termed dermal fibroblast conditioned medium (DFCM). Fibroblasts isolated from human skin samples were cultured in vitro using the serum-free keratinocyte-specific medium (Epilife (KM1), or define keratinocytes serum-free medium, DKSFM (KM2) and serum-free fibroblast-specific medium (FM) to collect DFCM-KM1, DFCM-KM2, and DFCM-FM, respectively). We characterised and evaluated the effects of 100-1600 µg/mL DFCM on keratinocytes based on attachment, proliferation, migration and gene expression. Supplementation with 200-400 µg/mL keratinocyte-specific DFCM-KM1 and DFCM-KM2 enhanced the attachment, proliferation and migration of sub-confluent keratinocytes, whereas 200-1600 µg/mL DFCM-FM significantly increased the healing rate in the wound healing assay, and 400-800 µg/mL DFCM-FM was suitable to enhance keratinocyte attachment and proliferation. A real-time (RT) profiler polymerase chain reaction (PCR) array showed that 42 genes in the DFCM groups had similar fold regulation compared to the control group and most of the genes were directly involved in wound healing. In conclusion, in vitro keratinocyte re-epithelialisation is supported by the fibroblast-secreted proteins in 200-400 µg/mL DFCM-KM1 and DFCM-KM2, and 400-800 µg/mL DFCM-FM, which could be useful for treating skin injuries.
成纤维细胞分泌许多重要的因子,可以从成纤维细胞培养基中收集,这被称为真皮成纤维细胞条件培养基(DFCM)。从人皮肤样本中分离的成纤维细胞在无血清角质形成细胞专用培养基(Epilife(KM1),或定义无血清角质形成细胞培养基,DKSFM(KM2)和无血清成纤维细胞专用培养基(FM)中进行体外培养,以分别收集 DFCM-KM1、DFCM-KM2 和 DFCM-FM)。我们根据附着、增殖、迁移和基因表达来描述和评估 100-1600μg/mL DFCM 对角质形成细胞的影响。补充 200-400μg/mL 角质形成细胞特异性 DFCM-KM1 和 DFCM-KM2 可增强亚汇合角质形成细胞的附着、增殖和迁移,而 200-1600μg/mL DFCM-FM 可显著提高伤口愈合试验中的愈合率,400-800μg/mL DFCM-FM 适合增强角质形成细胞附着和增殖。实时(RT)分析聚合酶链反应(PCR)阵列显示,DFCM 组中有 42 个基因与对照组相比具有相似的折叠调节,并且大多数基因直接参与伤口愈合。总之,200-400μg/mL DFCM-KM1 和 DFCM-KM2 以及 400-800μg/mL DFCM-FM 中的成纤维细胞分泌蛋白支持体外角质形成细胞再上皮化,这可能对治疗皮肤损伤有用。