Neuropilin‐2 is a novel marker expressed in pancreatic islet cells and endocrine pancreatic tumours

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Abstract
Neuropilin‐2 (NP‐2) is a cell surface transmembrane protein originally characterized as a receptor for the type 3 semaphorins, and more recently for a number of vascular endothelial growth factor (VEGF) isoforms. NP‐2 expression has been recently localized to a subset of neuroendocrine cells in the gastrointestinal tract. The aim of this study was to define the expression pattern of NP‐2 in normal pancreatic islets and to determine the utility of NP‐2 expression as a diagnostic marker of pancreatic endocrine tumours. Paraffin‐embedded tissue sections from 30 endocrine pancreatic tumours (EPTs) and from normal pancreas were immunostained with a rabbit polyclonal antibody generated towards NP‐2. Nineteen of the tumours were hormonally functional (nine insulinomas, nine gastrinomas, and one glucagonoma). The NP‐2 staining pattern was correlated with islet cell hormone expression. In addition, NP‐2 expression was evaluated in other normal neuroendocrine tissues and neuroendocrine neoplasms. In normal pancreas, NP‐2 stained a distinct subset of islet cells situated primarily at the islet periphery. Double immunohistochemical staining revealed co‐localization with glucagon‐expressing cells. Moderate to strong NP‐2 staining was present in 27 of 30 EPTs. Serial staining of the pancreatic tumours with insulin, gastrin, glucagon, pancreatic polypeptide (PP) or somatostatin did not reveal a distinct pattern of co‐localization. NP‐2 expression was not detected in neuroendocrine cells outside the gastroenteropancreatic system, or in their corresponding neoplasms, except for focal staining in one bronchial carcinoid tumour. In conclusion, the vast majority of EPTs examined expressed NP‐2, suggesting its utility as a diagnostic marker for these tumours. The function of NP‐2 in islet cell biology or tumourigenesis remains to be elucidated. Copyright © 2002 John Wiley & Sons, Ltd.

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