Cortical dendritic pathology in human immunodeficiency virus encephalitis.

E Masliah, N Ge, M Morey, R DeTeresa… - … ; a journal of technical …, 1992 - europepmc.org
E Masliah, N Ge, M Morey, R DeTeresa, RD Terry, CA Wiley
Laboratory investigation; a journal of technical methods and pathology, 1992europepmc.org
Previous neuropathological and morphometric studies of the cerebral cortex of patients with
human immunodeficiency virus encephalitis (HIVE) have shown a decrease in the
population of large neurons, moderate loss in synaptophysin immunoreactivity, and
pathological changes in dendrites. To further characterize and quantify alterations in the
dendritic tree of neocortical pyramidal neurons, we performed a modified Golgi impregnation
technique on Formalin fixed blocks from the frontal cortex of 5 HIVE cases, 5 human …
Previous neuropathological and morphometric studies of the cerebral cortex of patients with human immunodeficiency virus encephalitis (HIVE) have shown a decrease in the population of large neurons, moderate loss in synaptophysin immunoreactivity, and pathological changes in dendrites. To further characterize and quantify alterations in the dendritic tree of neocortical pyramidal neurons, we performed a modified Golgi impregnation technique on Formalin fixed blocks from the frontal cortex of 5 HIVE cases, 5 human immunodeficiency virus seropositive control cases without encephalitis, and 5 human immunodeficiency virus seronegative controls. Apical dendrites of HIVE cases were dilated, vacuolated, and tortuous with decreased length and branching. Basal and oblique dendrites also showed these alterations, but to a lesser extent. Some dendrites presented lacunae and filopodia consistent with remodeling. Computer aided quantification of HIVE cases showed a 40-60% decrease in spine density throughout the entire length of dendrites. Laser confocal imaging of Golgi impregnated sections displayed aberrant spines in regions of abnormal second order dendritic branches. These observations support the role of primary dendritic damage in HIVE in contrast to other neurodegenerative disorders where the primary pathology is presynaptic.
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