Bioprinting of human primary and iPSC-derived islets with retained and comparable functionality Article Swipe
Miranda Poklar
,
K. Ravikumar
,
Connor Wiegand
,
Ben Mizerak
,
Ruiqi Wang
,
Rodrigo M. Florentino
,
Zhenghao Liu
,
Alejandro Soto–Gutiérrez
,
Prashant N. Kumta
,
Ipsita Banerjee
·
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.1088/1758-5090/ade933
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.1088/1758-5090/ade933
Currently, type 1 diabetes (T1D) can be treated through implantation of allogenic islets, which replenish the beta cell population, however this method requires an extensive post-implantation immunosuppressant regimen. Personalized cellular therapy can address this through implantation of an autologous cell population, induced pluripotent stem cells (iPSCs). Cellular therapy, however, requires an encapsulation device for implantation, and so to achieve this uniformly with cells in a clinical setting, bioprinting is a useful option. Bioprinting is dependent on having a bioink that is printable, retains structural fidelity after printing, and is supportive of cell type and function. While bioprinting of pancreatic islets has been demonstrated previously, success in maintaining islet function post-printing has been varied. The objective of this study is to investigate the feasibility of printing functional islets by determining the appropriate combination of bioink, printing parameters, and cell configuration. Here, we detail the successful bioprinting of both primary human islets and iPSC-derived islets embedded in an alginate/methylcellulose bioink, with functionality sustained within the construct for both cell lineages. Sc-RNAseq analysis also revealed that printing did not adversely affect the genetic expression and metabolic functionality of the iPSC-derived islets. Importantly, the iPSC-derived islets displayed comparable functionality to the primary islets, indicating the potential to act as a cell source alternative for T1D implantation.
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Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1088/1758-5090/ade933
- OA Status
- hybrid
- References
- 78
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4412427387
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4412427387Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.1088/1758-5090/ade933Digital Object Identifier
- Title
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Bioprinting of human primary and iPSC-derived islets with retained and comparable functionalityWork title
- Type
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articleOpenAlex work type
- Language
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enPrimary language
- Publication year
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2025Year of publication
- Publication date
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2025-07-01Full publication date if available
- Authors
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Miranda Poklar, K. Ravikumar, Connor Wiegand, Ben Mizerak, Ruiqi Wang, Rodrigo M. Florentino, Zhenghao Liu, Alejandro Soto–Gutiérrez, Prashant N. Kumta, Ipsita BanerjeeList of authors in order
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https://doi.org/10.1088/1758-5090/ade933Publisher landing page
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YesWhether a free full text is available
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hybridOpen access status per OpenAlex
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https://doi.org/10.1088/1758-5090/ade933Direct OA link when available
- Concepts
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Induced pluripotent stem cell, Islet, 3D bioprinting, Population, Regenerative medicine, Cell, Cell biology, Tissue engineering, Biomedical engineering, Chemistry, Medicine, Biology, Diabetes mellitus, Endocrinology, Biochemistry, Embryonic stem cell, Gene, Environmental healthTop concepts (fields/topics) attached by OpenAlex
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0Total citation count in OpenAlex
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78Number of works referenced by this work
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10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.demonstrated | 103 |
| abstract_inverted_index.iPSC-derived | 152, 187, 191 |
| abstract_inverted_index.implantation | 10, 36 |
| abstract_inverted_index.encapsulation | 52 |
| abstract_inverted_index.functionality | 160, 184, 195 |
| abstract_inverted_index.implantation, | 55 |
| abstract_inverted_index.implantation. | 212 |
| abstract_inverted_index.post-printing | 110 |
| abstract_inverted_index.configuration. | 139 |
| abstract_inverted_index.immunosuppressant | 27 |
| abstract_inverted_index.post-implantation | 26 |
| abstract_inverted_index.alginate/methylcellulose | 157 |
| cited_by_percentile_year | |
| countries_distinct_count | 1 |
| institutions_distinct_count | 10 |
| citation_normalized_percentile.value | 0.4321352 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | True |