Concentration Dependent Effect of Human Dermal Fibroblast Conditioned Medium (DFCM) from Three Various Origins on Keratinocytes Wound Healing

被引:10
|
作者
Maarof, Manira [1 ]
Chowdhury, Shiplu Roy [1 ]
Saim, Aminuddin [2 ]
Idrus, Ruszymah Bt Hj [1 ,3 ]
Lokanathan, Yogeswaran [1 ]
机构
[1] Univ Kebangsaan Malaysia, Tissue Engn Ctr, Fac Med, Jalan Yaccob Latif, Kuala Lumpur 56000, Malaysia
[2] Ampang Puteri Specialist Hosp, Ear Nose & Throat Consultant Clin, 1 Jalan Mamanda 9, Ampang 68000, Selangor, Malaysia
[3] Univ Kebangsaan Malaysia, Dept Physiol, Fac Med, Jalan Yaccob Latif, Kuala Lumpur 56000, Malaysia
关键词
keratinocytes; fibroblasts; dermal fibroblast conditioned medium; tissue engineering; IN-VITRO; SKIN SUBSTITUTES; EXTRACELLULAR-MATRIX; PROLIFERATION; REPAIR; CELLS;
D O I
10.3390/ijms21082929
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 mu g/mL DFCM on keratinocytes based on attachment, proliferation, migration and gene expression. Supplementation with 200-400 mu g/mL keratinocyte-specific DFCM-KM1 and DFCM-KM2 enhanced the attachment, proliferation and migration of sub-confluent keratinocytes, whereas 200-1600 mu g/mL DFCM-FM significantly increased the healing rate in the wound healing assay, and 400-800 mu g/mL DFCM-FM was suitable to enhance keratinocyte attachment and proliferation. A real-time (RT2) 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 mu g/mL DFCM-KM1 and DFCM-KM2, and 400-800 mu g/mL DFCM-FM, which could be useful for treating skin injuries.
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页数:19
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