The dynamic interactions between B-ALL blasts and niche cells (vascular ECs, perivascular mesenchymal stem cells, and osteoblasts) were studied, identifying specific roles of these cells in regulating cytokines, adhesive signaling, and downstream B-ALL survival pathways, as well as markers of proliferation and quiescence, highlighting a subtype-related heterogeneity and responses to treatment
Factors (such as GABA and urocortin 3) released by the -cells stimulate somatostatin secretion, thereby providing a mechanism for feedback control of insulin and glucagon secretion during hyperglycaemia
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