Congenital or fetal hydrocephalus (FH) is one of the most common neurological disorders of newborns. It is often associated with head enlargement, accumulating cerebrospinal fluid (CSF) and neurological impairment. There are no curative therapies for hydrocephalus and therapies are generally limited to palliative, surgical approaches that utilize shunts to remove excess CSF. This proposal builds upon a recently reported link between a lipid signaling system and FH: lysophospholipids (LPs) that include LPA (lysophosphatidic acid), S1P (sphingosine 1-phosphate), and other related LPs. Present in blood, LPs could be part of the explanation for the observation that fetal bleeding increases the incidence of FH. This study will develop and characterize an animal model that recapitulates multiple, comorbid histological phenomena in the brain while producing FH. It will also determine the linkage between animal models and human FH by examining human FH CSF and brain tissue. Over a 5-year period, three aims will test the hypothesis that LP receptor mechanisms contribute to the etiology and therapeutic tractability of human FH.
Aim 1 will identify LPA chemical forms, including precursors and metabolites, from human hydrocephalic CSF, and assess their ability to induce FH and co-morbid CNS structural changes. Samples obtained through clinical collaborators and brain banks will be assessed towards establishing links between human FH and these animal models.
Aim 2 will determine cellular and molecular mechanisms contributing to the development of LPA-induced FH and comorbid changes, and assess their prevention or therapy via targeted agents.
This aim will provide new mechanistic insights that have therapeutic potential.
Aim 3 will identify new LP mechanisms with therapeutic potential contributing to FH and associated co-morbid changes.
This aim could expand the lipid influences on FH and offer distinct therapeutic targets for its treatment. Completion of these aims could open new mechanistic and therapeutic understanding for this common and debilitating disorder.

Public Health Relevance

Congenital or fetal hydrocephalus is among the most common neurological disorders of newborns and young children, for which there is limited understanding and no disease-modifying medicinal therapies. We have developed a mouse model based upon lysophospholipid signaling that provides mechanistic insights and therapeutic potential. This proposal will characterize the human relevance of the model, determine new mechanisms, and enhance the potential for medicinal FH treatment.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56NS082092-01A1
Application #
8549520
Study Section
Developmental Brain Disorders Study Section (DBD)
Program Officer
Morris, Jill A
Project Start
2012-09-30
Project End
2014-08-31
Budget Start
2012-09-30
Budget End
2014-08-31
Support Year
1
Fiscal Year
2012
Total Cost
$649,405
Indirect Cost
$299,405
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Yung, Yun C; Stoddard, Nicole C; Mirendil, Hope et al. (2015) Lysophosphatidic Acid signaling in the nervous system. Neuron 85:669-82
Chrencik, Jill E; Roth, Christopher B; Terakado, Masahiko et al. (2015) Crystal Structure of Antagonist Bound Human Lysophosphatidic Acid Receptor 1. Cell 161:1633-43
Stoddard, Nicole C; Chun, Jerold (2015) Promising pharmacological directions in the world of lysophosphatidic Acid signaling. Biomol Ther (Seoul) 23:1-11
Sheng, Xiaoyan; Yung, Yun C; Chen, Allison et al. (2015) Lysophosphatidic acid signalling in development. Development 142:1390-5
Mirendil, H; Thomas, E A; De Loera, C et al. (2015) LPA signaling initiates schizophrenia-like brain and behavioral changes in a mouse model of prenatal brain hemorrhage. Transl Psychiatry 5:e541
Yung, Yun C; Stoddard, Nicole C; Chun, Jerold (2014) LPA receptor signaling: pharmacology, physiology, and pathophysiology. J Lipid Res 55:1192-214
Wu, Daniel Dongwei; Zhang, Fuqiang; Hao, Feng et al. (2014) Matricellular protein Cyr61 bridges lysophosphatidic acid and integrin pathways leading to cell migration. J Biol Chem 289:5774-83
Lee, Sei-Jung; Leoni, Giovanna; Neumann, Philipp-Alexander et al. (2013) Distinct phospholipase C-? isozymes mediate lysophosphatidic acid receptor 1 effects on intestinal epithelial homeostasis and wound closure. Mol Cell Biol 33:2016-28