This request for a continuation of support is for longitudinal research designed to reveal basic principles and cellular mechanisms underlying development of the primate nervous system. In the next cycle of this grant, emphasis will be on (1) mechanisms of neuronal migration that include identification of binding molecule(s) and relative speed of cell translocation under normal and altered conditions; (2) the determinants of cell phenotypes and emergence of cytochemical individuality of neurons in developing primate brain under normal and experimentally altered conditions; (3) the capacity for postdevelopmental neurogenesis in primates; (4) development of synaptic connectivity and biochemical maturation of the """"""""extrapyramidal"""""""" motor system in developing normal monkeys and monkeys lesioned at critical embryonic ages; and (5) correlation of critical developmental periods as defined in experimental studies on developing monkey with corresponding stages based on various morphological and cytochemical criteria applied in postmortem human fetal brain.
Each Specific Aim consists of several interrelated experiments designed to use a battery of various light, electronmicroscopic and immunocytochemical methods including Golgi impregnation, Nissl-stain, histochemistry (e.g., AChE, monoamine fluorescence), immunocytochemistry (using a variety of antibodies), 3H-TdR autoradiography, anterograde and/or retrograde transport of radioactive tracers, HRP, or various fluorescent dyes. Our ability to perform intrauterine neurosurgery with short and long survival periods not only provides an opportunity to study the emergence of connections, but to change connectivity and explore experimentally the role of cell-to-cell interaction in morphological and biochemical maturation of the central nervous system. Until recently, experimental manipulation of early developmental processes has been the domain of research in simpler and peripheral nervous systems. In this project, as in the past, all studies will be performed on the developing rhesus monkey, with the conviction that the results will contribute to a greater understanding of mechanisms in normal brain development and help to uncover the etiology and pathogenesis of developmental brain disorders in man.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS014841-08
Application #
3395792
Study Section
Neurology B Subcommittee 1 (NEUB)
Project Start
1979-05-01
Project End
1991-04-30
Budget Start
1985-05-01
Budget End
1986-04-30
Support Year
8
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Yale University
Department
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
Morozov, Yury M; Sun, Yu-Yo; Kuan, Chia-Yi et al. (2016) Alteration of SLP2-like immunolabeling in mitochondria signifies early cellular damage in developing and adult mouse brain. Eur J Neurosci 43:245-57
Rash, Brian G; Ackman, James B; Rakic, Pasko (2016) Bidirectional radial Ca(2+) activity regulates neurogenesis and migration during early cortical column formation. Sci Adv 2:e1501733
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Hashimoto-Torii, Kazue; Torii, Masaaki; Fujimoto, Mitsuaki et al. (2014) Roles of heat shock factor 1 in neuronal response to fetal environmental risks and its relevance to brain disorders. Neuron 82:560-72
Radonji?, Nevena V; Ayoub, Albert E; Memi, Fani et al. (2014) Diversity of cortical interneurons in primates: the role of the dorsal proliferative niche. Cell Rep 9:2139-51
Rash, Brian G; Rakic, Pasko (2014) Neuroscience. Genetic resolutions of brain convolutions. Science 343:744-5

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