Modulation of neuronal thread protein expression with neuritic sprouting: Relevance to Alzheimer's disease

被引:25
作者
delaMonte, SM
Xu, YY
Wands, JR
机构
[1] HARVARD UNIV, SCH MED,MASSACHUSETTS GEN HOSP,MGH CANC CTR, ALZHEIMERS DIS RES CTR,DIV NEUROPATH, BOSTON, MA USA
[2] HARVARD UNIV, SCH MED,MASSACHUSETTS GEN HOSP,MGH CANC CTR, DEPT MED, BOSTON, MA USA
关键词
neuronal thread protein; retinoic acid; primitive neuroectodermal tumor; cell growth and differentiation; gene expression; Alzheimer's disease;
D O I
10.1016/0022-510X(95)00350-B
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Widespread proliferation of dystrophic neurites in the cerebral cortex represents an important neuroanatomical correlate of dementia in Alzheimer's disease (AD). Increased CNS expression of the 21-kDa neuronal thread protein (NTP) species is also correlated with dementia in AD. Pilot in vitro experiments provided evidence that high-level NTP expression might be linked to neuritic growth, The present stud!: examines retinoic acid (RA) modulation of NTP expression during neurite outgrowth and neuronal differentiation in SH-Sy5y neuroblastoma and PNET2 CNS-derived cells. In both cell lilies, RA-induced neuronal differentiation resulted in increased synthesis, expression, and phosphorylation of several al NTP species, with high steady-state levels and stepwise hyper-phosphorylation of 21-kDa NTP molecules. With neurite outgrowth, NTP molecules were translocated fi om the perikarya to long, slender, unbranched cell processes (axons) and growth cones. RA-mediated changes in NTP expression were independent oi DNA synthesis. The findings suggest that high-level expression of 21-kDa, and closely related phosphorylated NTP molecules correlates with neuritic growth. Therefore, over-expression of 21-kDa NTP molecules in AD probably reflects the widespread cortical neuritic sprouting associated with dementia. In view of the rapid phosphorylation and cell process translocation of NTP that occurs during neurite outgrowth in vitro, the accumulation of NTP in AD cortical neuronal perikarya suggests a further problem related to post-translational processing and transport of NTP molecules in AD neurodegeneration.
引用
收藏
页码:26 / 35
页数:10
相关论文
共 61 条
[1]
INCREASED PKA AND PKC ACTIVITIES ACCOMPANY NEURONAL DIFFERENTIATION OF NT2 D1 CELLS [J].
ABRAHAM, I ;
SAMPSON, KE ;
POWERS, EA ;
MAYO, JK ;
RUFF, VA ;
LEACH, KL .
JOURNAL OF NEUROSCIENCE RESEARCH, 1991, 28 (01) :29-39
[2]
Ausubel FM, 1995, CURRENT PROTOCOLS MO
[3]
A MEMBRANE PHOSPHOPROTEIN ASSOCIATED WITH NEURAL DEVELOPMENT, AXONAL REGENERATION, PHOSPHOLIPID-METABOLISM, AND SYNAPTIC PLASTICITY [J].
BENOWITZ, LI ;
ROUTTENBERG, A .
TRENDS IN NEUROSCIENCES, 1987, 10 (12) :527-532
[4]
BIEDLER JL, 1973, CANCER RES, V33, P2643
[5]
A68 PROTEINS IN ALZHEIMERS-DISEASE ARE COMPOSED OF SEVERAL TAU ISOFORMS IN A PHOSPHORYLATED STATE WHICH AFFECTS THEIR ELECTROPHORETIC MOBILITIES [J].
BRION, JP ;
HANGER, DP ;
COUCK, AM ;
ANDERTON, BH .
BIOCHEMICAL JOURNAL, 1991, 279 :831-836
[6]
CORK LC, 1986, J NEUROPATH EXP NEUR, V45, P56, DOI 10.1097/00005072-198601000-00005
[7]
DECARO AM, 1987, EUR J BIOCHEM, V168, P201
[8]
PHOSPHOPROTEIN B-50 IN NERVE GROWTH CONES FROM FETAL-RAT BRAIN [J].
DEGRAAN, PNE ;
VANHOOFF, COM ;
TILLY, BC ;
OESTREICHER, AB ;
SCHOTMAN, P ;
GISPEN, WH .
NEUROSCIENCE LETTERS, 1985, 61 (03) :235-241
[9]
DIAGNOSTIC UTILITY OF QUANTITATING NEUROFILAMENT-IMMUNOREACTIVE ALZHEIMERS-DISEASE LESIONS [J].
DELAMONTE, SM ;
WANDS, JR .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1994, 42 (12) :1625-1634
[10]
ENHANCED EXPRESSION OF AN EXOCRINE PANCREATIC PROTEIN IN ALZHEIMERS-DISEASE AND THE DEVELOPING HUMAN BRAIN [J].
DELAMONTE, SM ;
OZTURK, M ;
WANDS, JR .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (03) :1004-1013