4.8 Article

3D Bioprinting a human iPSC-derived MSC-loaded scaffold for repair of the uterine endometrium

Journal

ACTA BIOMATERIALIA
Volume 116, Issue -, Pages 268-284

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2020.09.012

Keywords

3D bioprinting; Human iPSC-derived mesenchymal stem cell; Endometrium; Regeneration; Curettage; Hydrogel scaffold; Endometrial receptivity

Funding

  1. General Guidance Project of Guangzhou Municipal Health Commission [20191A011023]
  2. Medical Scientific Research Foundation of Guangdong Province of China [A2020233]
  3. Guangzhou Institute of Pediatrics/Guangzhou Women and Children's Medical Center [YIP-2018-008]

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Common events in the clinic, such as uterine curettage or inflammation, may lead to irreversible endometrial damage, often resulting in infertility in women of childbearing age. Currently, tissue engineering has the potential to achieve tissue manipulation, regeneration, and growth, but personalization and precision remain challenges. The application of 3D cell printing is more in line with the clinical requirements of tissue repair. In this study, a porous grid-type human induced pluripotent stem cell-derived mesenchymal stem cell (hiMSC)-loaded hydrogel scaffold was constructed using a 3D bioprinting device. The 3D-printed hydrogel scaffold provided a permissive in vitro living environment for hiMSCs and significantly increased the survival duration of transplanted hiMSCs when compared with hiMSCs administered locally in vivo. Using an endometrial injury model, we found that hiMSC transplantation can cause early host immune responses (the serological immune response continued for more than 1 month, and the local immune response continued for approximately 1 week). Compared with the sham group, although the regenerative endometrium failed to show full restoration of the normal structure and function of the lining, implantation of the 3D-printed hiMSC-loaded scaffold not only promoted the recovery of the endometrial histomorphology (endometrial tissue and gland regeneration) and the regeneration of endometrial cells (stromal cells and epithelial cells) and endothelial cells but also improved endometrial receptivity functional indicators, namely, pinopode formation and leukemia inhibitory factor and alpha v beta 3 expression, which partly restored the embryo implantation and pregnancy maintenance functions of the injured endometrium. These indicators were significantly better in the 3D-printed hiMSC-loaded scaffold group than in the unrepaired (empty) group, the hiMSCs alone group and the 3D scaffold group, and the empty group showed the worst repair results. Our study confirm that the 3D-printed hiMSC-loaded hydrogel scaffold may be a promising material for endometrial repair. (C) 2020 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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