Project 3: Expression of developmentally regulated proteins in hypoxia. Chronic hypoxia in the early postnatal period is becoming an increasingly frequent occurrence. The neurodevelopmental consequences of early hypoxia can be severe. If we are to develop strategies to prevent the cognitive and behavioral deficits that result from early postnatal hypoxia, we must first gain a better understanding of the neurobiological consequences of hypoxic insult. In this project we will consider the effects of early hypoxia on the development of the molecular composition of the brain. We will compare normal to hypoxic animals through development and into adulthood to determine if hypoxia induces alterations in the normal time course of expression of several neural proteins and genes. Preliminary studies have shown that the expression of several important developmentally regulated proteins in perturbed by neonatal hypoxia. Abnormal structure/function of the brain as a consequence of insult in the early postnatal period could reflect a delay in normal developmental processes, or a precocious arrest of development. Either of these mechanisms would lead to the abnormalities observed in the hypoxic model used here.
The first aim of this project is to determine if periods of early postnatal hypoxia lead to abnormalities in the expression of developmentally regulated neural proteins. The results of these experiments will permit us to distinguish between developmental delay and developmental arrest as potential mechanisms underlying alterations caused by early postnatal hypoxia. """"""""Critical periods"""""""" in development, during which the structure and function of neurons can be modified by neuronal activity, have been documented in many areas of the nervous system. Abnormal neuronal activity during these critical periods can lead to irreversible abnormalities in neuronal structure and function. In considering management of infants with early postnatal hypoxia, it is essential to determine if there is a """"""""critical period"""""""" during which hypoxia lead to permanent neurological abnormalities.
The second aim of this project is to determine if there are """"""""critical periods"""""""" for the abnormalities that result from hypoxia. We will establish the time window during which hypoxia produces irreversible changes in neural properties.

Project Start
1998-05-01
Project End
1999-04-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
2
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Yale University
Department
Type
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Komitova, Mila; Xenos, Dionysios; Salmaso, Natalina et al. (2013) Hypoxia-induced developmental delays of inhibitory interneurons are reversed by environmental enrichment in the postnatal mouse forebrain. J Neurosci 33:13375-87
Silbereis, John; Heintz, Tristan; Taylor, Mary Morgan et al. (2010) Astroglial cells in the external granular layer are precursors of cerebellar granule neurons in neonates. Mol Cell Neurosci 44:362-73
Fagel, Devon M; Ganat, Yosif; Cheng, Elise et al. (2009) Fgfr1 is required for cortical regeneration and repair after perinatal hypoxia. J Neurosci 29:1202-11
Silbereis, John; Cheng, Elise; Ganat, Yosif M et al. (2009) Precursors with glial fibrillary acidic protein promoter activity transiently generate GABA interneurons in the postnatal cerebellum. Stem Cells 27:1152-63
Madri, J A (2009) Modeling the neurovascular niche: implications for recovery from CNS injury. J Physiol Pharmacol 60 Suppl 4:95-104
Chahboune, Halima; Ment, Laura R; Stewart, William B et al. (2009) Hypoxic injury during neonatal development in murine brain: correlation between in vivo DTI findings and behavioral assessment. Cereb Cortex 19:2891-901
Rauch, Millicent Ford; Michaud, Michael; Xu, Hao et al. (2008) Co-culture of primary neural progenitor and endothelial cells in a macroporous gel promotes stable vascular networks in vivo. J Biomater Sci Polym Ed 19:1469-85
Constable, R Todd; Ment, Laura R; Vohr, Betty R et al. (2008) Prematurely born children demonstrate white matter microstructural differences at 12 years of age, relative to term control subjects: an investigation of group and gender effects. Pediatrics 121:306-16
Li, Qi; Michaud, Michael; Stewart, William et al. (2008) Modeling the neurovascular niche: murine strain differences mimic the range of responses to chronic hypoxia in the premature newborn. J Neurosci Res 86:1227-42
Glantz, Susan B; Cianci, Carol D; Iyer, Rathna et al. (2007) Sequential degradation of alphaII and betaII spectrin by calpain in glutamate or maitotoxin-stimulated cells. Biochemistry 46:502-13

Showing the most recent 10 out of 45 publications