Your browser doesn't support javascript.
loading
Modulation of naïve mesenchymal stromal cells by extracellular vesicles derived from insulin-producing cells: an in vitro study.
Gabr, Mahmoud M; El-Halawani, Sawsan M; Refaie, Ayman F; Khater, Sherry M; Ismail, Amani M; Karras, Mary S; Magar, Raghda W; Sayed, Shorouk El; Kloc, Malgorzata; Uosef, Ahmed; Sabek, Omaima M; Ghoneim, Mohamed A.
Affiliation
  • Gabr MM; Biotechnology Department, Urology and Nephrology Center, Mansoura, Egypt.
  • El-Halawani SM; Biotechnology Department, Urology and Nephrology Center, Mansoura, Egypt.
  • Refaie AF; Nephrology Department, Urology and Nephrology Center, Mansoura, Egypt.
  • Khater SM; Pathology Department, Urology and Nephrology Center, Mansoura, Egypt.
  • Ismail AM; Immunology Department, Urology and Nephrology Center, Mansoura, Egypt.
  • Karras MS; Immunology Department, Urology and Nephrology Center, Mansoura, Egypt.
  • Magar RW; Immunology Department, Urology and Nephrology Center, Mansoura, Egypt.
  • Sayed SE; Microbiology Department, Faculty of Veterinary Medicine, Zagazig University, Zagazig, Egypt.
  • Kloc M; The Houston Methodist Research Institute, Houston, TX, USA.
  • Uosef A; Department of Surgery, Houston Methodist Hospital, Houston, TX, USA.
  • Sabek OM; Department of Genetics, MD Anderson Cancer Center, University of Texas, Houston, TX, USA.
  • Ghoneim MA; The Houston Methodist Research Institute, Houston, TX, USA.
Sci Rep ; 14(1): 17844, 2024 08 01.
Article in En | MEDLINE | ID: mdl-39090166
ABSTRACT
This study was to determine whether extracellular vesicles (EVs) derived from insulin-producing cells (IPCs) can modulate naïve mesenchymal stromal cells (MSCs) to become insulin-secreting. MSCs were isolated from human adipose tissue. The cells were then differentiated to generate IPCs by achemical-based induction protocol. EVs were retrieved from the conditioned media of undifferentiated (naïve) MSCs (uneducated EVs) and from that of MSC-derived IPCs (educated EVs) by sequential ultracentrifugation. The obtained EVs were co-cultured with naïve MSCs.The cocultured cells were evaluated by immunofluorescence, flow cytometry, C-peptide nanogold silver-enhanced immunostaining, relative gene expression and their response to a glucose challenge.Immunostaining for naïve MSCs cocultured with educated EVs was positive for insulin, C-peptide, and GAD65. By flow cytometry, the median percentages of insulin-andC-peptide-positive cells were 16.1% and 14.2% respectively. C-peptide nanogoldimmunostaining providedevidence for the intrinsic synthesis of C-peptide. These cells released increasing amounts of insulin and C-peptide in response to increasing glucose concentrations. Gene expression of relevant pancreatic endocrine genes, except for insulin, was modest. In contrast, the results of naïve MSCs co-cultured with uneducated exosomes were negative for insulin, C-peptide, and GAD65. These findings suggest that this approach may overcome the limitations of cell therapy.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Differentiation / Coculture Techniques / Insulin-Secreting Cells / Mesenchymal Stem Cells / Extracellular Vesicles / Insulin Limits: Humans Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: Egipto Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Differentiation / Coculture Techniques / Insulin-Secreting Cells / Mesenchymal Stem Cells / Extracellular Vesicles / Insulin Limits: Humans Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: Egipto Country of publication: Reino Unido