A J Kenny

An immunohistochemical study of endopeptidase-24.11 (“enkephalinase”) in the pig nervous system

Endopeptidase-24.11, a plasma membrane ectoenzyme with the ability to hydrolyse a variety of neuropeptides, has been localized in the pig nervous system by an immunoperoxidase technique. The endopeptidase was mapped in cryostat sections of the fore and mid-brain to the following structures: caudate-putamen, globus pallidus, olfactory tubercle, nucleus interpeduncularis and substantia nigra. Endopeptidase-24.11-like immunoreactivity was also found in the pia mater, choroid plexus and ependymal lining of the central canal. In the spinal cord, weak staining was observed in the dorsal horn, but strong staining was found in the dorsal root ganglia and nerve roots. Within the central nervous system, endopeptidase immunoreactivity was confined to gray matter and within the positive areas of the striatum densely staining areas, corresponding to striosomes, were discernible. These well-defined structures were exploited in serial sections to examine the alignment of the enzyme-rich patches of neuropil with correspondingly strong staining for other antigens. A consistent match was observed with a monoclonal antibody to neurofilament protein, but there was a poor correlation with a polyclonal antibody to glial fibrillary acidic protein. Substance P-like and [Leu]enkephalin-like immunoreactivity were also studied in sections adjacent to those stained for the endopeptidase. Good matching between enzyme-rich and peptide-rich areas was observed, but some enkephalin-rich areas did not align with enzyme staining and indeed endopeptidase-rich areas were not necessarily matched with areas rich in either peptide. These findings suggest a neuronal rather than an astrocytic location for endopeptidase-24.11 in the CNS and lend support to the view that it plays a central role in neuropeptide metabolism at membrane surfaces. In the peripheral nervous system, the endopeptidase was located in Schwann cell membranes surrounding dorsal root ganglion cells and nerve fibres, while in the pituitary the main concentration was in the adenohypophysis, where only a proportion of the endocrine cells were found to be immunoreactive.

An immunoelectron microscopic study of pig substantia nigra shows co-localization of endopeptidase-24.11 with substance P

Endopeptidase-24.11 is a widely distributed cell surface enzyme with a role in inactivating some neuropeptides and peptide hormones. In the central nervous system it has been implicated in the metabolism of enkephalins and tachykinins, neuropeptides which are expressed by neurons projecting to the substantia nigra. Two immunochemical methods have been used to reveal the ultrastructural localization of endopeptidase-24.11 and substance P in the substantia nigra of piglets. In the first approach, substance P was revealed by immunoperoxidase staining using the rat monoclonal antibody, NC1, and endopeptidase-24.11 by 1 nm colloidal gold using an affinity-purified rabbit polyclonal antibody, both being applied at the pre-embedding stage. NC1 was shown to be highly specific for substance P, with negligible cross-reactivity with neurokinins A and B. The specificity of the immunostaining was confirmed by processing all sections for both markers, even when only one primary antibody was applied. In the second approach, ultrathin cryosections were immunostained using gold particles of different diameters. In a survey of electron micrographs, 80% of the silver-enhanced gold particles were touching neuronal membranes, consistent with the known topology of endopeptidase-24.11. Endopeptidase-24.11 immunoreactivity was observed both on membranes of axons and on pre- and postsynaptic elements. Substance P immunoreactivity was seen within some boutons, apparently associated with vesicles, and in axons. In doubly stained sections, many examples of immunopositive gold-labelled boutons (i.e. endopeptidase-24.11-immunoreactive-positive) containing immunoperoxidase reaction product (i.e. substance P-immunoreactive-positive) were recorded. In ultrathin cryosections, substance P immunoreactivity was mainly observed in dense-core vesicles within boutons, some of which also showed membrane-associated gold particles marking endopeptidase-24.11 immunoreactivity. This is the first demonstration of endopeptidase-24.11 by immunogold at the electron microscopic level and the first demonstration of the ultrastructural co-localization of a membrane peptidase and its putative neuropeptide target. The results lend strong support to the view that endopeptidase-24.11 has a physiological role in the metabolism of substance P, but do not exclude a role in the inactivation of other neuropeptides.