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Hair-bearing human skin generated entirely from pluripotent stem cells

Jiyoon Lee, Cyrus Rabbani, Hongyu Gao, Matthew Steinhart, Benjamin M. Woodruff, Zachary Pflum, Alexander Kim, Stefan Heller, Yunlong Liu, Taha Z. Shipchandler, Karl R. Koehler

Preprint posted on July 08, 2019 https://www.biorxiv.org/content/10.1101/684282v1

  The Koehler lab has established complex skin organoids which sprout hair follicles and develop neurons.

Selected by Debbie Ho

Categories: developmental biology

Background

While in vitro culture of epidermal and dermal cells have provided some insights into skin diseases, it has been challenging to produce skin which forms and maintains hair follicles in vitro.

Last year, the Koehler lab successfully made organoids which produce hair follicles by differentiating mouse pluripotent stem cells (PSCs) into epidermal and dermal cells (Lee et al., 2018). They found that the 3D structure coupled with cross-talk between epidermal and dermal precursors were crucial to instruct the formation of hair follicles. In this preprint, the lab focussed on using human PSCs (hPSCs) to make follicle-bearing organoids by co-induction of epidermal and dermal fates.

Key Findings

The authors first induced an epidermal fate in hPSCs by treatment with BMP4 and a TGFb inhibitor, followed by mesenchymal fate induction by addition of FGF-2 and a BMP inhibitor. In the first two weeks of differentiation, the cell aggregates first formed a cyst of epithelial cells surrounded by cranial neural crest cells. Between day 16 – 30 of differentiation, the organoids become bipolar with the epidermal cyst on one side (referred to as the head) and neural crest cell derivatives on a pole (referred to as the tail). These results were consistent between organoids derived from two cell lines, a human embryonic stem cell line WA25 and a Desmoplakin (DSP)-GFP human induced-PSC (hiPSC) line, in which desmosomes would be GFP+.

To classify the cell types present at one month of differentiation, Lee et al. did single-cell RNA sequencing (scRNA-seq) on both the WA25 and DSP-GFP­ organoids. Analysis was done on each dataset individually and also comparatively to find differences and similarities between the cell lines. Unbiased clustering followed by manual partitioning revealed four major cell types: approximately two-thirds were mesenchymal cells, with smaller populations of epidermal cells, neuro-glial cells, and actively cycling cells. The cellular composition was mostly similar between organoids derived from both cell lines.

When WA25 and DSP-GFP organoids were cultured for 70 days, a duration at which foetal hair follicles typically form during gestation, hair germ-like buds emerged from the outer surface. At 120 days of differentiation, more than 80% of organoids formed hair follicles in each cell line, respectively. Furthermore, the gene expression of epidermal and dermal cells were consistent with that of human foetal hair follicles. Taken together, the data shows that the development of the hair follicles in these skin organoids replicate the well-documented morphological stages in development.

At >100 days of culture, the authors investigated whether more specialised cell types developed. The organoid hair follicles formed cellular layers characteristic of mammalian hair. Furthermore, in late-stage organoids, hyaline cartilage developed in the tail region and adipocytes were present around the hair follicles. Neurons also grew in interwoven networks between hair follicles, with their processes wrapped around the follicles, resembling human foetal hair follicles. The cartilage and neural populations possibly matured from the precursors identified in the scRNA-seq dataset at 30 days-post differentiation, which suggested a continuation of development over time in these organoids.

To investigate whether organoids could integrate into endogenous skin in a mammal, the authors matured the organoids for about 5 months and grafted hair-bearing organoids onto athymic nude mice. Out of 27 xenografts, around half of the organoids grew hairs out from the skin. Vasculature penetrated into xenografts and the organoids unfurled and integrated into planar skin at the wound site. The out-grown xenograft hair-follicles formed sebaceous glands and bulge cells, which are hallmarks of maturity.

Why this work is important

Lee et al. have established a new organoid model of skin development in a human system in which hair follicles and neurons emerge. Since the model captures aspects of human foetal skin development, it can be used to understand early development in vitro. Furthermore, heritable skin disorders could be modelled with this system for the purposes of discovering novel therapies. Finally, these hair-bearing organoids have the potential as grafts for repairing and reconstructing the skin of burned or injured patients.

Future directions and questions

  • The neurons in the organoids were able to form nerve endings. It would be interesting to check for markers of neuronal subtypes and use functional assays to characterise the type of nerve endings (mechanosensing, temperature-sensitive etc.).
  • As the authors mentioned, it will be worthwhile to investigate whether the xenografted hair follicles will start and complete a growth cycle.
  • In addition to Wnt signalling, are there patterning mechanisms shown in vertebrate embryos which are recapitulated in the organoids?

References

Lee, J., Bӧscke, R., Tang, P.C., Hartman, B.H., Heller, S. and Koehler, K.R., 2018. Hair follicle development in mouse pluripotent stem cell-derived skin organoids. Cell reports22(1), pp.242-254.

 

 

 

Posted on: 31st July 2019 , updated on: 1st August 2019

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