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Chinese Journal of Cell and Stem Cell(Electronic Edition) ›› 2019, Vol. 09 ›› Issue (05): 267-275. doi: 10.3877/cma.j.issn.2095-1221.2019.05.003

Special Issue:

• Original Research • Previous Articles     Next Articles

Isolation and identification of multidirectional differentiation of human skin fibroblasts

Chuanfei Wei1, Wei Wang1, Yanming Liu1, Jing Duan1, Xianjie Lu1, Yan Wang1, Nan Zhang1, Mengpeng Li1, Chao Chen1, Yang Zhang1, Jiabei Tong2, Fabin Han3,()   

  1. 1. The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng University/The Liaocheng People's Hospital, Liaocheng 252000, China
    2. Shandong Meijia Saipei Biotechnology Co., Ltd. Jinan 250000, China
    3. The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng University/The Liaocheng People's Hospital, Liaocheng 252000, China; Institute of Translational Medicine, The Second Hospital of Shandong University, Jinan 250000, China
  • Received:2019-08-03 Online:2019-10-01 Published:2019-10-01
  • Contact: Fabin Han
  • About author:
    Corresponding author: Han Fabin, Email:

Abstract:

Objective

To efficiently isolate human skin fibroblast cells with rapid proliferation and to investigate the multi-lineage differentiation potential of fibroblasts into adipogenic, osteogenic, chondrogenic and neurogenic directions.

Methods

The human primary fibroblast cells were isolated and cultured from the skin tissues. Morphological structures, flow cytometry and vimentin staining were used to identify the fibroblasts. Growth curves analysis, mitochondrial staining and karyotype analysis were used to identify the cell state of different generations. And finally fibroblasts were induced to adipogenic, osteogenic, chondrogenic and neurogenic directions. The difference between cell proliferation rate and the relative amount of mitochondrial was compared by t-test.

Results

The isolated fibroblasts showed a typical spindle-like morphology. Flow cytometry analysis showed that the isolated cells were highly express fibroblast surface markers CD90 (NCF1, NCF2 accounted for 99.9%, 98.7%, respectively) and CD73 (NCF1, NCF2 accounted for 98.2%, 85.6%, respectively) , rarely express hematopoietic stem cell marker CD34 (NCF1, NCF2 accounted for 1.8%, 2.6%, respectively) . All the fibroblasts positively express vimentin, the positive rate was 100%. The results of growth curves analyse showed that there was no significant difference in cell proliferation rate among multiple passages (t = 1.586, P = 0.1567) . The relative content of mitochondria showed no significant difference (t = 0.664, P = 0.543) between the fifth generation (relative fluorescence intensity: 6876±577.8) and the 10th generation (relative fluorescence intensity: 7371 ± 471.9) of the same cell line. Karyotype analysis showed that the number of chromosomes was 46 and the morphology of chromosomes were similar during passage. The multi-lineage differentiation assay showed that the fibroblasts could express adipogenic, osteogenic, cartilaginous and neurogenic differentiation markers.

Conclusion

Isolated fibroblasts have adipogenic, osteogenic, chondrogenic, neurogenic multi-directional differentiation potential, which can meet the needs of preclinical studies and provide cell sources for bone trauma, cartilage injury and neurodegenerative diseases.

Key words: Skin fibroblasts, Explant culture, Flow cytometry analysis, Multidirectional differentiation

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