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Human postnatal Mesenchymal Stem Cell Derived Islets as a Model for Diabetes Research.
Avinash Kharat1, Bhawna Chandravanshi2, Avinash Sanap1
1Regenerative Medicine Laboratory, Dr. D. Y. Patil Dental College & Hospital, Dr. D. Y. Patil Vidyapeeth, Pimpri, Pune, India.
Current Diabetes Reviews
|December 15, 2020
Summary
Stem cell-derived Islet-Like Clusters (ILCs) offer a promising alternative to human cadaver islets for Diabetes Mellitus (DM) treatment and drug testing, especially where cadaver islets are restricted.
Area of Science:
- Endocrinology
- Stem Cell Biology
- Regenerative Medicine
Background:
- Scarcity of human cadaver islets for transplantation in Diabetes Mellitus (DM) necessitates alternative sources.
- Stem cell-derived Islet-Like Clusters (ILCs) show potential for DM treatment and drug discovery.
- In vitro differentiation of ILCs mimics in vivo islet development but often results in immature cells.
Purpose of the Study:
- To review the utilization of ILCs from human postnatal tissues as an in vitro model.
- To discuss ILCs for cytotoxicity testing, drug screening, and enhancing transplantation efficacy.
- To explore ILCs as a platform for drug screening and stem cell-based DM treatment, particularly in regions with restrictions on cadaver islet research.
Main Methods:
- Review of current literature on stem cell-derived ILCs.
- Discussion of pharmacological preconditioning to improve ILC function.
- Analysis of ILC applications in drug screening and transplantation.
Main Results:
- Pharmacological preconditioning can enhance the in vitro and in vivo performance of ILCs.
- ILCs can serve as a reliable in vitro model for drug screening and cytotoxicity testing.
- ILCs offer a viable alternative to animal testing in drug discovery.
Conclusions:
- ILCs derived from human postnatal tissues are valuable for in vitro research and potential DM therapy.
- ILCs can complement, reduce, and potentially replace animal testing in drug screening.
- ILCs represent a significant advancement for in vitro screening and stem cell-based DM treatment, especially under research restrictions.
Keywords:
Diabetes mellitusdrug screeningglucose responsivenessinsulin secretionislet like clusterislet transplantation.
