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Review | Open Access

Sebaceous gland organoid engineering

Yiqiong Liu1,†, Huanhuan Gao1,† , Huating Chen1, Shuaifei Ji1, Lu Wu1, Hongliang Zhang1, Yujia Wang2, Xiaobing Fu1( ), Xiaoyan Sun1( )
Research Center for Tissue Repair and Regeneration affliated to the Medical Innovation Research Department and 4th Medical Center, PLA General Hospital and PLA Medical College; PLA Key Laboratory of Tissue Repair and Regenerative Medicine and Beijing Key Research Laboratory of Skin Injury, Repair and Regeneration; Research Unit of Trauma Care, Tissue Repair and Regeneration, Chinese Academy of Medical Sciences, 2019RU051, Beijing 100048, P. R. China
Queen Mary School of Nanchang University, Nanchang University, Nanchang, Jiangxi 330006, P. R. China

†Yiqiong Liu and Huanhuan Gao contributed equally to this work.

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Highlights

• Lrig1+ stem cells in SGs may offer the nearest hope for an ideal source of SG organoid engineering.

• Precise regulation of Wnt signaling spatially and temporally appear to be the key point to trigger SG organoid self-assembly appropriately.

• Synthetic polymer hydrogels are the most common source of matrix for the ease with which their biological and physical properties can be manipulated.

• Induced pluripotent stem cells and skin-specific endothelial progenitor cells are the ideal sources for SG organoid vascularization.

• Human SG organoids provide a near-authentic platform to study pathophysiology and discover potential drug targets of acne vulgaris.

Abstract

Sebaceous glands (SGs), as holocrine-secreting appendages, lubricate the skin and play a central role in the skin barrier. Large full-thickness skin defects cause overall architecture disruption and SG loss. However, an effective strategy for SG regeneration is lacking. Organoids are 3D multicellular structures that replicate key anatomical and functional characteristics of in vivo tissues and exhibit great potential in regenerative medicine. Recently, considerable progress has been made in developing reliable procedures for SG organoids and existing SG organoids recapitulate the main morphological, structural and functional features of their in vivo counterparts. Engineering approaches empower researchers to manipulate cell behaviors, the surrounding environment and cell–environment crosstalk within the culture system as needed. These techniques can be applied to the SG organoid culture system to generate functionally more competent SG organoids. This review aims to provide an overview of recent advancements in SG organoid engineering. It highlights some potential strategies for SG organoid functionalization that are promising to forge a platform for engineering vascularized, innervated, immune-interactive and lipogenic SG organoids. We anticipate that this review will not only contribute to improving our understanding of SG biology and regeneration but also facilitate the transition of the SG organoid from laboratory research to a feasible clinical application.

References

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Burns & Trauma
Article number: tkae003

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Cite this article:
Liu Y, Gao H, Chen H, et al. Sebaceous gland organoid engineering. Burns & Trauma, 2024, 12: tkae003. https://doi.org/10.1093/burnst/tkae003

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Received: 19 October 2023
Revised: 27 December 2023
Published: 10 October 2026
© The Author(s) 2024. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com