“…Merkel cells have been shown to contain low molecular cytokeratins (Saurat et al, 1984;Moll et al, 1984;Ortonne & Darmon, 1985;Ness et aI., 1987;Markl et al, 1989;Wollina, 1992), desmosomal proteins (Ortonne & Darmon, 1985) and neuroendocrine markers such as neuron-specific enolase (NSE) (Gu et al, 1983;Warner et al, 1983;Masuda et al, 1986), chromogranin (Ness et al, 1987;Hartschuh et al, 1989), substance P (Hartschuh et al,I989), peptide histidine isoleucin (PHI/PHM) (Hartschuh et al, 1989), calcitonin gene-related peptide (CGRP) (Hartschuh et al, 1989;Garcia-Caballero et al, 1989c) co-occurring with vasoactive intestinal polypeptide (VIP) (Alvarez et al,i988), VIP (Hartschuh et al, 1989), met-enkephalin (Hartschuh et al, 1979(Hartschuh et al, , 1986Warner et al, I983), leucine aminopeptidase (Tachibana et al, 1989) and synaptophysin (Ortonne et at., 1988;Garcia-Caballero et al, 1989a), and serotonin by GarciaCaballero et al (1989b). The above studies show a fairly complete mapping of Merkel cell populations in various mammalian species.…”