TY - JOUR
T1 - Glial fibrillary acidic protein immunoreactivity in the prefrontal cortex distinguishes younger from older adults in major depressive disorder
AU - Miguel-Hidalgo, José Javier
AU - Baucom, Christie
AU - Dilley, Ginny
AU - Overholser, James C.
AU - Meltzer, Herbert Y.
AU - Stockmeier, Craig A.
AU - Rajkowska, Grazyna
N1 - Funding Information:
This study was supported by funds from VISN 16 MIRECC (GR), NARSAD Independent Investigator Award (GR), and NIMH Grants Nos. MH55872 (GR) and MH45488 (CAS). We acknowledge the excellent assistance of the Cuyahoga County Coroner’s Office in Cleveland, Ohio. The authors thank Zoltan Makkos, M.D., (National Institute of Psychiatry and Neurology, Budapest, Hungary) for technical help with the GFAP staining, and Lisa Konick (Case Western Reserve University, Cleveland, Ohio, USA) for assistance in collecting information on many of the subjects under study.
PY - 2000/10/15
Y1 - 2000/10/15
N2 - Background: Recent postmortem studies in major depressive disorder (MDD) provide evidence for a reduction in the packing density and number of glial cells in different regions of the prefrontal cortex; however, the specific types of glia involved in those morphologic changes are unknown. Methods: The territory occupied by the astroglial marker glial fibrillary acidic protein (GFAP) was measured as an areal fraction in cortical layers III, IV, and V in sections from the dorsolateral prefrontal cortex (dlPFC) of MDD and control subjects. In addition, the packing density of GFAP-immunoreactive somata was measured by a direct three-dimensional cell counting method. Results: The mean areal fraction and packing density of GFAP-immunoreactive astrocytes in the dlPFC of MDD subjects were not significantly different from those in control subjects; however, in MDD there was a significant strong positive correlation between age and GFAP immunoreactivity. When the MDD group was divided into younger (30-45 years old) and older (46-86) adults, in the five younger MDD adults, areal fraction and packing density were smaller than the smallest values of the control subjects. In contrast, among older MDD subjects these parameters tended to be greater than in the older control subjects. Conclusions: The present results suggest that the GFAP-immunoreactive astroglia is differentially involved in the pathology of MDD in younger compared with older adults. (C) 2000 Society of Biological Psychiatry.
AB - Background: Recent postmortem studies in major depressive disorder (MDD) provide evidence for a reduction in the packing density and number of glial cells in different regions of the prefrontal cortex; however, the specific types of glia involved in those morphologic changes are unknown. Methods: The territory occupied by the astroglial marker glial fibrillary acidic protein (GFAP) was measured as an areal fraction in cortical layers III, IV, and V in sections from the dorsolateral prefrontal cortex (dlPFC) of MDD and control subjects. In addition, the packing density of GFAP-immunoreactive somata was measured by a direct three-dimensional cell counting method. Results: The mean areal fraction and packing density of GFAP-immunoreactive astrocytes in the dlPFC of MDD subjects were not significantly different from those in control subjects; however, in MDD there was a significant strong positive correlation between age and GFAP immunoreactivity. When the MDD group was divided into younger (30-45 years old) and older (46-86) adults, in the five younger MDD adults, areal fraction and packing density were smaller than the smallest values of the control subjects. In contrast, among older MDD subjects these parameters tended to be greater than in the older control subjects. Conclusions: The present results suggest that the GFAP-immunoreactive astroglia is differentially involved in the pathology of MDD in younger compared with older adults. (C) 2000 Society of Biological Psychiatry.
KW - Aging
KW - Astroglia
KW - Dorsolateral prefrontal cortex
KW - Human postmortem
KW - Neuropathology
KW - Quantitative immunohistochemistry
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U2 - 10.1016/S0006-3223(00)00999-9
DO - 10.1016/S0006-3223(00)00999-9
M3 - Article
C2 - 11063981
AN - SCOPUS:0034667321
VL - 48
SP - 861
EP - 873
JO - Biological Psychiatry
JF - Biological Psychiatry
SN - 0006-3223
IS - 8
ER -