3D GelMA-Printing of Pancreatic Endocrine Constructs via Magnetic Chitosan Nanoparticle-Mediated CRISPR/dCas9a Delivery: A Proof-of-Concept Study

Diabetes mellitus affects nearly half a billion people worldwide and is primarily caused by the loss of insulin-producing cells, which are essential for maintaining normal blood glucose levels. In this study, we optimized a CRISPR activation (CRISPRa) system based on deactivated Cas9 (dCas9) to transfect HEK293 cells, which were subsequently differentiated into functional α-, β-, and δ-like cells as an engineering proof-of-concept. The CRISPRa system targeted multiple genes, including NGN3, NKX6.1 + MAFA, and PDX1, successfully inducing cell differentiation as confirmed by immunostaining. These cells were encapsulated in a 3D-printed GelMA disk, and the secretion of glucagon, insulin, and somatostatin was monitored for 30 days.

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Publication Details

Journal
Macromol—A Journal of Macromolecular Research
Published
2026-09-28
DOI
https://doi.org/10.3390/macromol6040085
Primary Topic
3D Printing in Biomedical Research
Type
article
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article

3D GelMA-Printing of Pancreatic Endocrine Constructs via Magnetic Chitosan Nanoparticle-Mediated CRISPR/dCas9a Delivery: A Proof-of-Concept Study

Yi‐Chen Ethan Li, Mei‐Hwa Lee, Chien-Yu Lin, Hung-Yin Lin et al.
Macromol—A Journal of Macromolecular Research
3D Printing in Biomedical Research
article

3D GelMA-Printing of Pancreatic Endocrine Constructs via Magnetic Chitosan Nanoparticle-Mediated CRISPR/dCas9a Delivery: A Proof-of-Concept Study

Yi‐Chen Ethan Li, Mei‐Hwa Lee, Chien-Yu Lin, Hung-Yin Lin, Yu-Ling Lin
article en

Abstract

Diabetes mellitus affects nearly half a billion people worldwide and is primarily caused by the loss of insulin-producing cells, which are essential for maintaining normal blood glucose levels. In this study, we optimized a CRISPR activation (CRISPRa) system based on deactivated Cas9 (dCas9) to transfect HEK293 cells, which were subsequently differentiated into functional α-, β-, and δ-like cells as an engineering proof-of-concept. The CRISPRa system targeted multiple genes, including NGN3, NKX6.1 + MAFA, and PDX1, successfully inducing cell differentiation as confirmed by immunostaining. These cells were encapsulated in a 3D-printed GelMA disk, and the secretion of glucagon, insulin, and somatostatin was monitored for 30 days.

Macromol—A Journal of Macromolecular ResearchVol. 6(4)
National University of Kaohsiung (TW), Feng Chia University (TW), I-Shou University (TW)
Good health and well-being
Openalex Percentile: Top 22%
3D Printing in Biomedical Research
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