Key result
Co-culturing human islets with bone marrow stem cells significantly upregulated angiogenesis factors such as VEGF-a (535 vs 2 pg/mL) and promoted islet vascularization in vitro.
Why the study?
Does co-culture with human bone marrow stem cells improve angiogenesis and regeneration in human pancreatic islets in vitro?
Does co-culture with human bone marrow stem cells improve angiogenesis and regeneration in human pancreatic islets in vitro?
Absolute Event Rate: 535% vs 2%
p-value: p=<0.01
Co-culturing human pancreatic islets with bone marrow stem cells promotes islet vascularization and endocrine cell regeneration via upregulation of angiogenesis factors in vitro.
No clinical role yet for islet transplantation; hypothesis-generating for in vivo vascularization and engraftment studies.
BM stem cells may have regenerative effects on islet function through angiogenesis. Human islets (100islet equivalent/mL) were cultured alone (control) or co-cultured (experimental group) with whole human BM (1 × 10(6) cells/mL) for 210 days. A protein array measuring angiogenesis factors found upregulated (experimental vs control, day 210) proteins levels of VEGF-a (535 vs 2 pg/mL), PDGF (280.79 vs 0 pg/mL), KGF (939 vs 8 pg/mL), TIMP-1 (4592 vs 4332 pg/mL) and angiogenin (506 vs 97 pg/mL). Lower protein levels of angiopoietin-2 (5 vs 709 pg/mL) were observed. Depletion of pro-angiogenesis factors in co-culture decreased the effects of BM-induced islet vascularization. Depletion of VEGF-a, eKGF and PDGF significantly reduced islet vascularization but individual depletion of KGF and PDGF had less effects overall on vessel formation. BM-induced vascularization showed significant endothelial cell distribution. Islet vascularization was linked to islet growth. A decrease in islet size indicated poor vascularization. Insulin release was evident in the tissues generated from human islet-BM co-culture throughout the entire culture period. Significant increase in insulin (28.66-fold vs control) and glucagon (24.4-fold vs control) gene expression suggest BM can induce endocrine cell regeneration. In conclusion, BM promotes human islet tissue regeneration via regulation of angiogenesis factors.
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Luo et al. (2010) studied Islet transplantation (in vitro). Co-culture with whole human bone marrow cells vs. Human islets cultured alone was evaluated on VEGF-a protein levels at day 210 (pg/mL) (p=<0.01). Co-culturing human islets with bone marrow stem cells significantly upregulated angiogenesis factors such as VEGF-a (535 vs 2 pg/mL) and promoted islet vascularization in vitro.
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