TY - JOUR
T1 - Human pancreatic islets produce and secrete MCP-1/CCL2
T2 - Relevance in human islet transplantation
AU - Piemonti, Lorenzo
AU - Leone, Biagio Eugenio
AU - Nano, Rita
AU - Saccani, Alessandra
AU - Monti, Paolo
AU - Maffi, Paola
AU - Bianchi, Giancarlo
AU - Sica, Antonio
AU - Peri, Giuseppe
AU - Melzi, Raffaella
AU - Aldrighetti, Luca
AU - Secchi, Antonio
AU - Di Carlo, Valerio
AU - Allavena, Paola
AU - Bertuzzi, Federico
PY - 2002
Y1 - 2002
N2 - We investigated the capacity of human islets to produce monocyte chemoattractant protein-1 (MCP-1). Primary cultures of pancreatic islets expressed and secreted MCP-1, as determined by Northern blot, immunohistochemistry, in situ hybridization, and enzyme-linked immunosorbent assay. The produced MCP-1 was biologically active as it attracted monocytes in chemotaxis assay, and chemotactic activity was almost abrogated by a neutralizing anti-MCP-1 monoclonal antibody. Expression of MCP-1 was increased by primary inflammatory cytokines (interleukin-1β, tumor necrosis factor-α) and lipopolysaccharide at both the mRNA and protein levels but not by glucose. However, MCP-1 did not modulate insulin secretion. MCP-1 secreted by pancreatic islets plays a relevant role in the clinical outcome of islet transplant in patients with type 1 diabetes. In fact, low MCP-1 secretion resulted as the most relevant factor for long-lasting insulin independence. This finding opens new approaches in the management of human islet transplantation. Finally, the finding that MCP-1 appears constitutively present in normal human islet β-cells (immunohistochemistry and in situ hybridization), in the absence of an inflammatory infiltrate, suggests that this chemokine could have functions other than monocyte recruitment and opens a new link between the endocrine and immune systems.
AB - We investigated the capacity of human islets to produce monocyte chemoattractant protein-1 (MCP-1). Primary cultures of pancreatic islets expressed and secreted MCP-1, as determined by Northern blot, immunohistochemistry, in situ hybridization, and enzyme-linked immunosorbent assay. The produced MCP-1 was biologically active as it attracted monocytes in chemotaxis assay, and chemotactic activity was almost abrogated by a neutralizing anti-MCP-1 monoclonal antibody. Expression of MCP-1 was increased by primary inflammatory cytokines (interleukin-1β, tumor necrosis factor-α) and lipopolysaccharide at both the mRNA and protein levels but not by glucose. However, MCP-1 did not modulate insulin secretion. MCP-1 secreted by pancreatic islets plays a relevant role in the clinical outcome of islet transplant in patients with type 1 diabetes. In fact, low MCP-1 secretion resulted as the most relevant factor for long-lasting insulin independence. This finding opens new approaches in the management of human islet transplantation. Finally, the finding that MCP-1 appears constitutively present in normal human islet β-cells (immunohistochemistry and in situ hybridization), in the absence of an inflammatory infiltrate, suggests that this chemokine could have functions other than monocyte recruitment and opens a new link between the endocrine and immune systems.
UR - http://www.scopus.com/inward/record.url?scp=0036094994&partnerID=8YFLogxK
U2 - 10.2337/diabetes.51.1.55
DO - 10.2337/diabetes.51.1.55
M3 - Article
SN - 0012-1797
VL - 51
SP - 55
EP - 65
JO - Diabetes
JF - Diabetes
IS - 1
ER -