: The goal of the proposed project is to define the synergistic roles of presenilins (PS1 and PS2) in cortical development and Notch signaling. Our previous studies of the PS1-null mouse revealed a role for PS1 in early neurogenesis and the regulation of Notch signaling. The perinatal lethality and the cerebral hemorrhage associated with PS1/- mice preclude a complete study of PS1 function in neuronal migration and cortical layer formation during later embryonic and postnatal stages. Furthermore, the early embryonic lethality (about 9) of the PS1PS2 -/-mice prevents the investigation of the role of both presenilins (PS) in cortical development and Notch signaling. We have therefore developed a viable PS1 conditional knockout (PS1cKO) mouse, in which Psi1 function is selectively eliminated in neural progenitor cells beginning at E9 and subsequently in the entire neuronal and glial populations. The PS1 cKO mouse allows us to generate a double cKO (PS1cKO; PS2-/-) lacking both PS in neural progenitor cells. Analysis of the PS1 single and PS1/PS2 double cKO mice will elucidate the role of PS1 and PS2 in neurogenesis, neuronal migration and Notch signaling during development. The significance of the proposed study is our characterization of the effects of partial and complete loss of PS function in vivo, the results of which would be applicable to the use of PS as therapeutic targets for anti-amyloidogenic therapy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS042818-05
Application #
6984756
Study Section
Special Emphasis Panel (ZRG1-MDCN-2 (01))
Program Officer
Owens, David F
Project Start
2001-12-15
Project End
2008-07-31
Budget Start
2005-12-01
Budget End
2008-07-31
Support Year
5
Fiscal Year
2006
Total Cost
$328,592
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
Kelleher 3rd, Raymond J; Shen, Jie (2017) Presenilin-1 mutations and Alzheimer's disease. Proc Natl Acad Sci U S A 114:629-631
Kang, Jongkyun; Shin, Sarah; Perrimon, Norbert et al. (2017) An Evolutionarily Conserved Role of Presenilin in Neuronal Protection in the Aging Drosophila Brain. Genetics 206:1479-1493
Lee, Sang Hun; Lutz, David; Mossalam, Mohanad et al. (2017) Presenilins regulate synaptic plasticity and mitochondrial calcium homeostasis in the hippocampal mossy fiber pathway. Mol Neurodegener 12:48
Watanabe, Hirotaka; Shen, Jie (2017) Dominant negative mechanism of Presenilin-1 mutations in FAD. Proc Natl Acad Sci U S A 114:12635-12637
Xia, Dan; Kelleher 3rd, Raymond J; Shen, Jie (2016) Loss of A?43 Production Caused by Presenilin-1 Mutations in the Knockin Mouse Brain. Neuron 90:417-22
Xia, Dan; Watanabe, Hirotaka; Wu, Bei et al. (2015) Presenilin-1 knockin mice reveal loss-of-function mechanism for familial Alzheimer's disease. Neuron 85:967-81
Shen, Jie (2014) Function and dysfunction of presenilin. Neurodegener Dis 13:61-3
Lee, Sang Hun; Sharma, Manu; Südhof, Thomas C et al. (2014) Synaptic function of nicastrin in hippocampal neurons. Proc Natl Acad Sci U S A 111:8973-8
Watanabe, Hirotaka; Iqbal, Minah; Zheng, Jin et al. (2014) Partial loss of presenilin impairs age-dependent neuronal survival in the cerebral cortex. J Neurosci 34:15912-22
Yamaguchi, Hiroo; Shen, Jie (2013) Histological analysis of neurodegeneration in the mouse brain. Methods Mol Biol 1004:91-113

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