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The homing of exogenous hair follicle mesenchymal stem cells into hair follicle niches
Kaitao Li, Fang Liu, Ye He, Qian Qu, Pingping Sun, Lijuan Du, Jin Wang, Ruosi Chen, Yuyang Gan, Danlan Fu, Zhexiang Fan, Bingcheng Liu, Zhiqi Hu, Yong Miao
Kaitao Li, Fang Liu, Ye He, Qian Qu, Pingping Sun, Lijuan Du, Jin Wang, Ruosi Chen, Yuyang Gan, Danlan Fu, Zhexiang Fan, Bingcheng Liu, Zhiqi Hu, Yong Miao
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Research Article Dermatology Stem cells

The homing of exogenous hair follicle mesenchymal stem cells into hair follicle niches

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Abstract

Hair loss is a debilitating condition associated with the depletion of dermal papilla cells (DPCs), which can be replenished by dermal sheath cells (DSCs). Hence, strategies aimed at increasing the populations of DPCs and DSCs hold promise for the treatment of hair loss. In this study, we demonstrated in mice that introduced exogenous DPCs and DSCs (hair follicle mesenchymal stem cells) could effectively migrate and integrate into the dermal papilla and dermal sheath niches, leading to enhanced hair growth and prolonged anagen phases. However, the homing rates of DPCs and DSCs were influenced by various factors, including recipient mouse depilation, cell passage number, cell dose, and immune rejection. Through in vitro and in vivo experiments, we also discovered that the CXCL13/CXCR5 pathway mediated the homing of DPCs and DSCs into hair follicle niches. This study underscores the potential of cell-based therapies for hair loss by targeted delivery of DPCs and DSCs to their respective niches and sheds light on the intriguing concept that isolated mesenchymal stem cells can home back to their original niche microenvironment.

Authors

Kaitao Li, Fang Liu, Ye He, Qian Qu, Pingping Sun, Lijuan Du, Jin Wang, Ruosi Chen, Yuyang Gan, Danlan Fu, Zhexiang Fan, Bingcheng Liu, Zhiqi Hu, Yong Miao

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Figure 1

Exogenous hfMSCs home to HF niches, and depilation increases the homing rate.

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Exogenous hfMSCs home to HF niches, and depilation increases the homing ...
(A) Immunostaining for alkaline phosphatase, NCAM, and SOX2 in third-passage DPCs and for α-SMA, NCAM, and SOX2 in third-passage DSCs (representative of 3 experiments). (B) Representative HFs containing exogenous DPCs (arrow) or DSCs (arrow) 2 weeks after injection. Hatched lines denoted the DP (representative of 3 experiments). (C and D) Immunostaining for NCAM and α-SMA in HFs containing exogenous DPCs (arrow) or DSCs (arrow) (representative of 3 experiments). (E and F) HFs containing exogenous DPCs (arrow) or DSCs (arrow) were immunostained for NCAM 2 weeks after injection. The number of HFs containing EGFP+ cells and number of homing EGFP+ cells per ×100 original magnification field of view (n = 7 skin sections from 4 mice per group). Scale bars: 100 μm. Two-tailed Student’s t test. Data reported as mean ± SD. **P < 0.01, ***P < 0.001.

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