The proposed Senator Jacob Javits Center will be dedicated to research on the basic neurobiology of the primate neocortex. Although the site of dysfunction in a large share of neurological diseases and human suffering, the neocortex has not been the focus of a specific Institute or of a Center devoted to multidisciplinary research. A team of investigators with wide experience (molecular biology, cell biology, biochemistry, immunocytochemistry, electron microscopy, endocrinology, neuroanatomy, neurophysiology, pharmacology, psychobiology, computer engineering, veterinary medicine, neurosurgery and neuropathology) have joined forces to explore three major themes: [1] Organization, [2] Development, and [3] Modifiability of the neocortex in the rhesus monkey. Each theme will be studied at the molecular, structural, physiological and behavioral levels, and the design of these studies generally will allow the use of the same set of animals for multiple experiments. The first theme includes basic analysis of input-output relationships and microcircuitry of selected cortical areas, their transmitters, receptors and information processing properties. The second theme is built upon the first and includes genetic and epigenetic determinants of (molecular, structural and functional) neuronal phenotypes and development of their laminar, modular and regional positions; studies in this theme will also examine the mode and mechanisms of establishment of axonal connections and the sequence, tempo and pattern of synaptogenesis in selected cortical regions. The third theme concerns the molecular, anatomical and physiological modifiability of neocortex with emphasis on interactions between ipsilateral and contralateral cortico-cortical connections, afferents, cortico-subcortical and intrinsic microcircuitry. The techniques of prenatal neurosurgery will enable experimental manipulation of cortical development, its connections and synaptic organization at critical fetal ages. Studies will be carried out on the rhesus monkey with the intent of enhancing understanding of cellular mechanisms in normal cortical development and pathogenesis of disorders affecting higher cortical functions in humans. The Center will promote research collaboration and enable comprehensive, multipronged and quantitative analyses that have not been possible before now, and that would not be practical for individual investigators supported by separate research grants.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS022807-03
Application #
3099972
Study Section
(SRC)
Project Start
1985-09-01
Project End
1990-08-31
Budget Start
1987-09-01
Budget End
1988-08-31
Support Year
3
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Yale University
Department
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Quinn, Christopher C; Chen, Esteban; Kinjo, Tashi G et al. (2003) TUC-4b, a novel TUC family variant, regulates neurite outgrowth and associates with vesicles in the growth cone. J Neurosci 23:2815-23
Turner, Christopher P; Yan, Henglin; Schwartz, Michael et al. (2002) A1 adenosine receptor activation induces ventriculomegaly and white matter loss. Neuroreport 13:1199-204
Wasiak, S; Quinn, C C; Ritter, B et al. (2001) The Ras/Rac guanine nucleotide exchange factor mammalian Son-of-sevenless interacts with PACSIN 1/syndapin I, a regulator of endocytosis and the actin cytoskeleton. J Biol Chem 276:26622-8
Haydar, T F; Wang, F; Schwartz, M L et al. (2000) Differential modulation of proliferation in the neocortical ventricular and subventricular zones. J Neurosci 20:5764-74
Tong, X K; Hussain, N K; de Heuvel, E et al. (2000) The endocytic protein intersectin is a major binding partner for the Ras exchange factor mSos1 in rat brain. EMBO J 19:1263-71
Quinn, C C; Gray, G E; Hockfield, S (1999) A family of proteins implicated in axon guidance and outgrowth. J Neurobiol 41:158-64
Wang, F; Lidow, M S (1997) Alpha 2A-adrenergic receptors are expressed by diverse cell types in the fetal primate cerebral wall. J Comp Neurol 378:493-507
Redmond, L; Xie, H; Ziskind-Conhaim, L et al. (1997) Cues intrinsic to the spinal cord determine the pattern and timing of primary afferent growth. Dev Biol 182:205-18
Anton, E S; Cameron, R S; Rakic, P (1996) Role of neuron-glial junctional domain proteins in the maintenance and termination of neuronal migration across the embryonic cerebral wall. J Neurosci 16:2283-93
Fryer, H J; Hockfield, S (1996) The role of polysialic acid and other carbohydrate polymers in neural structural plasticity. Curr Opin Neurobiol 6:113-8

Showing the most recent 10 out of 73 publications