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Departments of Medicine and Histochemistry, Royal Postgraduate Medical School London W12 OHS, United Kingdom
Address all correspondence and requests for reprints to: Prof. S. R. Bloom, Department of Medicine, Royal Postgraduate Medical School, 2nd Floor, Francis Fraser Laboratory, Hammersmith Hospital, Du Cane Road, London W12 OHS, United Kingdom.
Galanin immunoreactivity was measured by RIA, using antibodies directed against both the non-C- and C-terminal positions of porcine galanin, in tissue extracts of normal adrenals and pheochromocytomas and also in the plasma of normal subjects and patients with pheochromocytomas. No C-terminal galanin-like immunoreactivity was detected in plasma or tissue, suggesting differences in the amino acid sequence of human compared with porcine galanin. A non-C-terminally directed antibody was, therefore, used to characterize human galanin immunoreactivity by gel permeation chromatography and reverse phase high pressure liquid chromatography and to localize it by immunocytochemistry. The galanin content of whole adrenal gland was 2.6 1 0.9 (1SEM) pmol/g (n = 5). In contrast, however, pheochromocytomas had much greater concentrations (21 1 2.3 pmol/g; n = 16).Gel chromatography and reverse phase high pressure liquid chromatography revealed 2 molecular forms of galanin immunoreactivity with identical elution positions in both normal adrenals and tumors. The concentration of galanin in plasma from both normal subjects and pheochromocytoma patients was below the detection limit of the assay (<10 pmol/liter). Using immunocytochemistry, galanin was localized to scattered cells or clusters of tumor cells in 5 of 11 pheochromocytomas and only a few chromaffin cells and cortical nerve fibers in normal adrenals.
Received April 7, 1986.
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