TY - JOUR
T1 - Development of human insulin-producing cells for cell therapy of diabetes
AU - Russ, Holger A.
AU - Efrat, Shimon
PY - 2011/12
Y1 - 2011/12
N2 - Diabetes mellitus is characterized by the loss of insulin-producing beta cells. While conventional treatment results in severe long-term complications, cell replacement therapy is a promising approach for the cure of this disease. However, its application is severally limited by the shortage of donor tissue. Hence, great research efforts concentrate on the development of an abundant cell source of functional beta-like cells, by pursuing three main strategies: Expansion of human donor beta cells in vitro, reprogramming of other cell types, and directed differentiation of pluripotent stem cells, both embryonic and patient-derived. The goal of all these approaches has been the generation of cells with properties that closely resemble the beta-cell phenotype, in particular production and storage of adequate amounts of mature insulin, and its regulated release in response to physiological signals. Here we review recent progress in all three approaches and discuss their advantases as well as remaining challenges.
AB - Diabetes mellitus is characterized by the loss of insulin-producing beta cells. While conventional treatment results in severe long-term complications, cell replacement therapy is a promising approach for the cure of this disease. However, its application is severally limited by the shortage of donor tissue. Hence, great research efforts concentrate on the development of an abundant cell source of functional beta-like cells, by pursuing three main strategies: Expansion of human donor beta cells in vitro, reprogramming of other cell types, and directed differentiation of pluripotent stem cells, both embryonic and patient-derived. The goal of all these approaches has been the generation of cells with properties that closely resemble the beta-cell phenotype, in particular production and storage of adequate amounts of mature insulin, and its regulated release in response to physiological signals. Here we review recent progress in all three approaches and discuss their advantases as well as remaining challenges.
KW - Beta-cell replication
KW - Nuclear reprogramming
KW - Pluripotent stem cells
UR - http://www.scopus.com/inward/record.url?scp=84858850212&partnerID=8YFLogxK
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AN - SCOPUS:84858850212
SN - 1565-4753
VL - 9
SP - 590
EP - 597
JO - Pediatric Endocrinology Reviews
JF - Pediatric Endocrinology Reviews
IS - 2
ER -