4.6 Article

Using bioprinting and spheroid culture to create a skin model with sweat glands and hair follicles

Journal

BURNS & TRAUMA
Volume 9, Issue -, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/burnst/tkab013

Keywords

Skin regeneration; Sweat glands; Hair follicle; 3D bioprinting; Spheroid culture; Skin constructs

Funding

  1. National Nature Science Foundation of China [81830064, 81721092, 81701906]
  2. National Key Research and Development Plan [2017YFC1103300]
  3. Funds of Chinese PLA General Hospital for Military Medical Innovation Research Project [CX19026]
  4. CAMS Innovation Fund for Medical Sciences (CIFMS) [2019-I2M-5-059]
  5. Military Medical Research and Development Projects [AWS17J005, 2019-126]
  6. Fostering Funds of Chinese PLA General Hospital for National Distinguished Young Scholar Science Fund [2017-JQPY-002]

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An in vitro model of skin constructs with sweat glands (SGs) and hair follicles (HFs) was established to explore the interaction between these two appendages in regeneration. The results showed that HF spheroids promoted differentiation of both SGs and HFs in SG scaffolds, while SG scaffolds mainly promoted SG differentiation and had little effect on HF potency in HF spheroids. The study provides insights into the molecular mechanisms of SG and HF regeneration.
Background: Sweat glands (SGs) and hair follicles (HFs) are two important cutaneous appendages that play crucial roles in homeostatic maintenance and thermoregulation, and their interaction is involved in wound healing. SGs can be regenerated from mesenchymal stem cell-laden 3D bioprinted scaffolds, based on our previous studies, whereas regeneration of HFs could not be achieved in the same model. Due to the lack of an in vitro model, the underlying molecular mechanism of the interaction between SGs and HFs in regeneration could not be fully understood. The purpose of the present study was to establish an in vitro model of skin constructs with SGs and HFs and explore the interaction between these two appendages in regeneration. Methods: To investigate the interaction effects between SGs and HFs during their regeneration processes, a combined model was created by seeding HF spheroids on 3D printed SG scaffolds. The interaction between SG scaffolds and HF spheroids was detected using RNA expression and immunofluorescence staining. The effects of microenvironmental cues on SG and HF regeneration were analysed by altering seed cell types and plantar dermis homogenate in the scaffold. Results: According to this model, we overcame the difficulties in simultaneously inducing SG and HF regeneration and explored the interaction effects between SG scaffolds and HF spheroids. Surprisingly, HF spheroids promoted both SG and HF differentiation in SG scaffolds, while SG scaffolds promoted SG differentiation but had little effect on HF potency in HF spheroids. Specifically, microenvironmental factors (plantar dermis homogenate) in SG scaffolds effectively promoted SG and HF genesis in HF spheroids, no matter what the seed cell type in SG scaffolds was, and the promotion effects were persistent. Conclusions: Our approach elucidated a new model for SG and HF formation in vitro and provided an applicable platform to investigate the interaction between SGs and HFs in vitro. This platform might facilitate 3D skin constructs with multiple appendages and unveil the spatiotemporal molecular program of multiple appendage regeneration.

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