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Immunohistochemical localization of intracellular plasma proteins in the human central nervous system
Authors:H. M. Liu  J. R. Atack  S. I. Rapoport
Affiliation:(1) Department of Pathology, Brown University and Miriam Hospital, 02906 Providence, RI, USA;(2) Laboratory of Neurosciences, National Institute on Aging, National Institutes of Health, Building 10, Room 6C103, 9000 Rockville Pike, 20892 Bethesda, MD, USA
Abstract:Summary The regional distribution of plasma protein immunoreactivity was studied in the postmortem central nervous system (CNS) of normal subjects 18 to 78 years old. Samples taken from various areas of brain and spinal cord were processed for peroxidase-antiperoxidase immunocytochemistry using polyclonal antibodies against plasma albumin, prealbumin, agr1-acid glycoprotein, agr1-macroglobulin, IgG, transferrin, haptoglobin, hemopexin, fibrinogen, as well against the glial fibrillary acidic and S-100 proteins. Many neurons of the spinal cord, cranial nerve nuclei, pontine nuclei, cerebellar dentate nucleus, red nucleus, thalamus and hypothalamus showed strong immunostaining for albumin and moderate to strong staining for agr1-acid, IgG, transferrin, haptoglobin, as well as relatively weak immunoreactivity against other plasma proteins. Less intense staining was seen in the nucleus basalis, putamen and Purkinje cells. In contrast, most cerebral cortical neurons were negative except for a few positively stained pyramidal neurons in the hippocampus and in layers III and V of the association neocortex, although more positive pyramidal neurons were observed in the motor and sensory neocortices. Reaction products were also seen in axons of motor and sensory long tracts. These findings suggest that plasma proteins may be transported to spinal cord and brain stem neurons by peripherally projecting nerves and that a series of anterograde and retrograde transneuronal transfers are responsible for the accumulation of plasma proteins in relay nuclei and in other CNS neurons.
Keywords:Plasma protein  Brain  Blood-brain barrier  Neuron  Aging
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