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Glucosamine potentiates the differentiation of adipose-derived stem cells into glucose-responsive insulin-producing cells.
Hong, Yeonhee; Park, Eun-Young; Kim, Donghee; Lee, Hakmo; Jung, Hye Seung; Jun, Hee-Sook.
Afiliación
  • Hong Y; College of Pharmacy and Gachon Institute of Pharmaceutical Science, Gachon University, Incheon, Republic of Korea.
  • Park EY; Lee Gil Ya Cancer and Diabetes Institute, Gachon University, Incheon, Republic of Korea.
  • Kim D; College of Pharmacy, Mokpo National University, Muan-gun, Jeonnam, Republic of Korea.
  • Lee H; Lee Gil Ya Cancer and Diabetes Institute, Gachon University, Incheon, Republic of Korea.
  • Jung HS; Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
  • Jun HS; Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Ann Transl Med ; 8(8): 561, 2020 Apr.
Article en En | MEDLINE | ID: mdl-32775362
ABSTRACT

BACKGROUND:

Islet transplantation might be a logical strategy to restore insulin secretion for the treatment of diabetes, however, the scarcity of donors poses an obstacle for such a treatment. As an alternative islet source, differentiation of stem cells into insulin-producing cells (IPCs) has been tried. Many protocols have been developed to improve the efficiency of differentiation of stem cells into IPCs. In this study, we investigated whether glucosamine supplementation during differentiation of human adipose-derived stem cells (hADSCs) into IPCs can improve the insulin secretory function.

METHODS:

Glucosamine was added to the original differentiation medium at different stages of differentiation of hADSCs into IPCs for 12 days and insulin secretion was analyzed.

RESULTS:

Addition of glucosamine alone to the growth medium of hADSCs did not affect the differentiation of hADSCs to IPCs. Supplementation of the differentiation medium with glucosamine at a later stage (protocol G3) proved to have the greatest effect on IPC differentiation. Basal and glucose-stimulated insulin secretion (GSIS) was significantly increased and the expression of insulin and C-peptide was increased in differentiated IPCs as compared with that in differentiated IPCs using the conventional protocol (protocol C). In addition, the expression of beta-cell specific transcription factors such as pancreatic and duodenal homeobox1 (PDX1) and neurogenin 3 (NGN3) was also increased. Furthermore, the expression of genes related to insulin secretion, including synaptotagmin 4 (Syt4), glucokinase (Gck) and glucose transporter 2 (Glut2), was also increased.

CONCLUSIONS:

We conclude that glucosamine supplementation potentiates the differentiation of hADSCs into IPCs.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Ann Transl Med Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Ann Transl Med Año: 2020 Tipo del documento: Article