Cell-replacement therapy for diabetes: Generating functional insulin-producing tissue from adult human liver cells
Cell therapy
Renal capsule
Human liver
Immunosuppression
DOI:
10.1073/pnas.0405277102
Publication Date:
2005-05-18T03:19:38Z
AUTHORS (16)
ABSTRACT
Shortage in tissue availability from cadaver donors and the need for life-long immunosuppression severely restrict large-scale application of cell-replacement therapy diabetic patients. This study suggests potential use adult human liver as alternate autologous beta-cell-replacement therapy. By using pancreatic duodenal homeobox gene 1 (PDX-1) soluble factors, we induced a comprehensive developmental shift cells into functional insulin-producing cells. PDX-1-treated express insulin, store it defined granules, secrete hormone glucose-regulated manner. When transplanted under renal capsule diabetic, immunodeficient mice, ameliorated hyperglycemia prolonged periods time. Inducing redirection offers diabetics by allowing patient to be donor his own tissue.
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