This revision of U24 l /lH068457-08, """"""""NIMH Center for Collaborative Studies on Mental Disorders,"""""""" (NIMHC) requests funding for a """"""""Repository Supporting Stem Cell Research Relevant to Mental Disorders"""""""" in response to NOT-MH-10-024. Since late 1998, the NIMHC, whose biorepository is at Rutgers University and whose data repository is at Washington University School of Medicine, has established a robust infrastructure for the receipt of blood samples and externally produced cell cultures. DNA and RNA has been extracted from blood and over 75,000 lymphoblastoid cell lines have been produced in-house for the NIMHC, with 99.8% success on the first attempt. In the past 5 years, the NIMHC has distributed -450,000 DNA, ~15,000 RNA and ~8,000 cell lines to researchers throughout the world. Based on serving the needs of NIMH Genetics Initiative grantees, the NIMHC maintains secure clinical (phenotypic) and genomic databases and a password protected, secure website for NIMH-approved researchers to access. The NIMHC has also developed and made available web-based bioinformatics resources for the design, analysis and interpretation of studies in psychiatric genetics. We propose to utilize the facilities, expertise and experience of the NIMHC to serve researchers wishing to use human patient and control primary cells, adult stem cells and induced pluripotent stem cells (iPSCs) for investigation of the cellular bases of mental disorders. The NIMHC will receive primary tissue samples for the establishment and banking of primary cell cultures or adult stem cell lines. The NIMHC will also receive cultures of primary cells, adult stem cells and iPSCs for characterization and banking. These cell lines, along with subject clinical and genomic data and molecular and phenotypic data describing the cell lines, will be distributed to NIMH-approved researchers. The NIMHC will also provide consultation regarding the nature and use of these stem cell lines. To a lesser extent, the NIMHC will also produce, characterize and bank iPSCs made from primary cells. Freely sharing primary and stem cells within the research community is likely to greatly accelerate progress in understanding the cellular bases of mental disorders. Public Health Relevance: Mental disorders are a common, widespread and heterogeneous group of diseases whose biological bases are poorly understood. Elucidation of the underlying genetic and physiological bases for these disorders is necessary for the creation of effective therapeutics. Nerve cells or other cells derived from adult stem cells offer the possibility of modeling these disorders in cell culture and for preliminary screening of pharmaceuticals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Resource-Related Research Projects--Cooperative Agreements (U24)
Project #
3U24MH068457-09S1
Application #
8151735
Study Section
Special Emphasis Panel (ZMH1-ERB-C (03))
Program Officer
Bender, Patrick
Project Start
2003-07-01
Project End
2013-05-31
Budget Start
2011-09-23
Budget End
2012-05-31
Support Year
9
Fiscal Year
2011
Total Cost
$895,000
Indirect Cost
Name
Rutgers University
Department
Genetics
Type
Schools of Arts and Sciences
DUNS #
001912864
City
New Brunswick
State
NJ
Country
United States
Zip Code
08901
Zhang, Tianxiao; Hou, Liping; Chen, David T et al. (2018) Exome sequencing of a large family identifies potential candidate genes contributing risk to bipolar disorder. Gene 645:119-123
Sun, N; Nasello, C; Deng, L et al. (2018) The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family. Mol Psychiatry 23:1487-1495
VAN DER Mee, Denise J; Fedko, Iryna O; Hottenga, Jouke-Jan et al. (2018) Dopaminergic Genetic Variants and Voluntary Externally Paced Exercise Behavior. Med Sci Sports Exerc 50:700-708
Abdulkadir, Mohamed; Londono, Douglas; Gordon, Derek et al. (2018) Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. Eur Arch Psychiatry Clin Neurosci 268:301-316
Culverhouse, R C; Saccone, N L; Horton, A C et al. (2018) Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression. Mol Psychiatry 23:133-142
Thornton, Laura M; Munn-Chernoff, Melissa A; Baker, Jessica H et al. (2018) The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methods. Contemp Clin Trials 74:61-69
Smit, Dirk J A; Wright, Margaret J; Meyers, Jacquelyn L et al. (2018) Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. Hum Brain Mapp 39:4183-4195
Hysi, Pirro G; Valdes, Ana M; Liu, Fan et al. (2018) Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Nat Genet 50:652-656
Van der Auwera, Sandra; Peyrot, Wouter J; Milaneschi, Yuri et al. (2018) Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD. Am J Med Genet B Neuropsychiatr Genet 177:40-49
Daneshjou, Roxana; Wang, Yanran; Bromberg, Yana et al. (2017) Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges. Hum Mutat 38:1182-1192

Showing the most recent 10 out of 107 publications