SPECIFICITY OF 192 IGG-SAPORIN FOR NGF RECEPTOR-POSITIVE CHOLINERGIC BASAL FOREBRAIN NEURONS IN THE RAT

被引:140
作者
BOOK, AA
WILEY, RG
SCHWEITZER, JB
机构
[1] UNIV TENNESSEE,CTR HLTH SCI,COLL MED,DEPT PATHOL,800 MADISON AVE,ROOM 568M,MEMPHIS,TN 38163
[2] UNIV TENNESSEE CTR HLTH SCI,DEPT ANAT & NEUROBIOL,MEMPHIS,TN 38163
[3] VET ADM MED CTR,NASHVILLE,TN 37203
[4] VANDERBILT UNIV,NASHVILLE,TN 37232
关键词
NERVE GROWTH FACTOR RECEPTOR; IMMUNOTOXIN; CHOLINE ACETYLTRANSFERASE; TYROSINE HYDROXYLASE; IMMUNOHISTOCHEMISTRY; RADIOENZYMATIC ASSAY;
D O I
10.1016/0006-8993(92)91121-T
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A monoclonal antibody to the rat nerve growth factor (NGF) receptor, 192 IgG, accumulates bilaterally and specifically in cholinergic basal forebrain (CBF) cells following intraventricular injection. An immunotoxin composed of 192 IgG linked to saporin (192 IgG-saporin) has been shown to destroy cholinergic neurons in the basal forebrain. We sought to determine if intraventricular 192 IgG-saporin affected choline acetyltransferase (ChAT) enzyme activity in the CBF terminal projection fields. ChAT assays from 192 IgG-saporin-treated animals showed significant time-dependent decreases in ChAT activity in the neocortex, olfactory bulb and hippocampus, compared to PBS- or OKT1-saporin-injected controls. ChAT and tyrosine hydroxylase activity in the striatum was always unchanged by 192 IgG-saporin. ChAT immunohistochemistry was confirmative of major cell loss in the CBF, while other cholinergic nuclei appeared unremarkable. The data provide further evidence of the selectivity of 192 IgG-saporin in abolishing cholinergic, NGF receptor-positive CNS neurons.
引用
收藏
页码:350 / 355
页数:6
相关论文
共 35 条
  • [1] CHANDLER CE, 1984, J BIOL CHEM, V259, P6882
  • [2] HEMICHOLINIUM-3 PREVENTS THE WORKING MEMORY IMPAIRMENTS AND THE CHOLINERGIC HYPOFUNCTION INDUCED BY ETHYLCHOLINE AZIRIDINIUM ION (AF64A)
    CHROBAK, JJ
    SPATES, MJ
    STACKMAN, RW
    WALSH, TJ
    [J]. BRAIN RESEARCH, 1989, 504 (02) : 269 - 275
  • [3] NUCLEUS BASALIS NEURONAL LOSS, NEURITIC PLAQUES AND CHOLINE-ACETYLTRANSFERASE ACTIVITY IN ADVANCED ALZHEIMERS-DISEASE
    ETIENNE, P
    ROBITAILLE, Y
    WOOD, P
    GAUTHIER, S
    NAIR, NPV
    QUIRION, R
    [J]. NEUROSCIENCE, 1986, 19 (04) : 1279 - 1291
  • [4] CHOLINERGIC MECHANISMS IN LEARNING, MEMORY AND DEMENTIA - A REVIEW OF RECENT-EVIDENCE
    FIBIGER, HC
    [J]. TRENDS IN NEUROSCIENCES, 1991, 14 (06) : 220 - 223
  • [5] BEHAVIORAL AND NEUROCHEMICAL EFFECTS FOLLOWING NEUROTOXIC LESIONS OF A MAJOR CHOLINERGIC INPUT TO THE CEREBRAL-CORTEX IN THE RAT
    FLICKER, C
    DEAN, RL
    WATKINS, DL
    FISHER, SK
    BARTUS, RT
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1983, 18 (06) : 973 - 981
  • [6] RETROGRADE CELL CHANGES IN MEDIAL SEPTUM AND DIAGONAL BAND FOLLOWING FIMBRIA-FORNIX TRANSECTION - QUANTITATIVE TEMPORAL ANALYSIS
    GAGE, FH
    WICTORIN, K
    FISCHER, W
    WILLIAMS, LR
    VARON, S
    BJORKLUND, A
    [J]. NEUROSCIENCE, 1986, 19 (01) : 241 - 255
  • [7] NGF RECEPTOR REEXPRESSION AND NGF-MEDIATED CHOLINERGIC NEURONAL HYPERTROPHY IN THE DAMAGED ADULT NEOSTRIATUM
    GAGE, FH
    BATCHELOR, P
    CHEN, KS
    CHIN, D
    HIGGINS, GA
    KOH, S
    DEPUTY, S
    ROSENBERG, MB
    FISCHER, W
    BJORKLUND, A
    [J]. NEURON, 1989, 2 (02) : 1177 - 1184
  • [8] LOCALIZATION OF NERVE GROWTH-FACTOR RECEPTORS IN CHOLINERGIC NEURONS OF THE HUMAN BASAL FOREBRAIN
    HEFTI, F
    HARTIKKA, J
    SALVATIERRA, A
    WEINER, WJ
    MASH, DC
    [J]. NEUROSCIENCE LETTERS, 1986, 69 (01) : 37 - 41
  • [9] CHOLINERGIC DEFICIT INDUCED BY ETHYLCHOLINE AZIRIDINIUM (AF64A) TRANSIENTLY AFFECTS SOMATOSTATIN AND NEUROPEPTIDE-Y LEVELS IN RAT-BRAIN
    HORTNAGL, H
    SPERK, G
    SOBAL, G
    MAAS, D
    [J]. JOURNAL OF NEUROCHEMISTRY, 1990, 54 (05) : 1608 - 1613
  • [10] JOHNSTON MV, 1981, EXP BRAIN RES, V43, P159