In vitro proliferation of cells derived from adult human β-cells revealed by cell-lineage tracing
OBJECTIVE—Expansion of insulin-producing β-cells from adult human islets could alleviate
donor shortage for cell-replacement therapy of diabetes. A major obstacle to development of
effective expansion protocols is the rapid loss of β-cell markers in the cultured cells. Here,
we report a genetic cell-lineage tracing approach for following the fate of cultured β-cells.
RESEARCH DESIGN AND METHODS—Cells dissociated from isolated human islets were
infected with two lentiviruses, one expressing Cre recombinase under control of the insulin …
donor shortage for cell-replacement therapy of diabetes. A major obstacle to development of
effective expansion protocols is the rapid loss of β-cell markers in the cultured cells. Here,
we report a genetic cell-lineage tracing approach for following the fate of cultured β-cells.
RESEARCH DESIGN AND METHODS—Cells dissociated from isolated human islets were
infected with two lentiviruses, one expressing Cre recombinase under control of the insulin …
OBJECTIVE— Expansion of insulin-producing β-cells from adult human islets could alleviate donor shortage for cell-replacement therapy of diabetes. A major obstacle to development of effective expansion protocols is the rapid loss of β-cell markers in the cultured cells. Here, we report a genetic cell-lineage tracing approach for following the fate of cultured β-cells.
RESEARCH DESIGN AND METHODS— Cells dissociated from isolated human islets were infected with two lentiviruses, one expressing Cre recombinase under control of the insulin promoter and the other, a reporter cassette with the structure cytomegalovirus promoter-loxP-DsRed2-loxP-eGFP.
RESULTS— β-Cells were efficiently and specifically labeled by the dual virus system. Label+, insulin− cells derived from β-cells were shown to proliferate for a maximum of 16 population doublings, with an approximate doubling time of 7 days. Isolated labeled cells could be expanded in the absence of other pancreas cell types if provided with medium conditioned by pancreatic non–β-cells. Analysis of mouse islet cells by the same method revealed a much lower proliferation of labeled cells under similar culture conditions.
CONCLUSIONS— Our findings provide direct evidence for survival and dedifferentiation of cultured adult human β-cells and demonstrate that the dedifferentiated cells significantly proliferate in vitro. The findings confirm the difference between mouse and human β-cell proliferation under our culture conditions. These findings demonstrate the feasibility of cell-specific labeling of cultured primary human cells using a genetic recombination approach that was previously restricted to transgenic animals.
Am Diabetes Assoc