PhD, University of Tokyo (JAPAN), Biochemistry and Molecular Biology
MS, University of Tokyo (JAPAN), Medical Science
B.Pharm., Meiji Pharmaceutical University (JAPAN), Pharmacy
2011-2014: HFSP Long-Term Fellowship
2009: Japanese Society of Neuroimmunology Award
Phenomena or Processes
G-Protein Coupled Receptors, Inflammation
Gupta S, Kihara Y, Maurya MR, Norris PC, Dennis EA, Subramaniam S
J Phys Chem B 2016 Aug 25 ;120(33):8346-53Kihara Y, Groves A, Rivera RR, Chun J
Ann Clin Transl Neurol 2015 Oct ;2(10):978-83Chrencik JE, Roth CB, Terakado M, Kurata H, Omi R, Kihara Y, Warshaviak D, Nakade S, Asmar-Rovira G, Mileni M, Mizuno H, Griffith MT, Rodgers C, Han GW, Velasquez J, Chun J, Stevens RC, Hanson MA
Cell 2015 Jun 18 ;161(7):1633-43Professor at UC San Diego and TSRI
Department Head, Molecular Neuroscience, Merck Research Labs
I love doing science, and a chance to do some good for the world. Sanford Burnham Prebys is a great place to pursue science.
1988-1991: Postdoctoral Fellow, Whitehead Institute/MIT, laboratories of Drs. Rudolf Jaenisch and David Baltimore, Developmental and Molecular Biology
1988: MD, PhD, Stanford University School of Medicine, Neuroscience
1981: B.A., University of Hawaii at Manoa, English and Biology
2016: Alzheimer’s San Diego Courage and Hope Award
2014: Thomson Reuters World’s Most Influential Scientific Minds list of highly cited researchers
2011: Killam Lecturer, Montreal Neurological Institute
2010: Journal of Lipid Research Lecturer, Keystone Symposium on Bioactive Lipids: Biochemistry and Diseases, Kyoto, Japan
2007: Chancellor’s Award for Excellence in Neuroscience, LSU Medical School
1999-2006: Independent Scientist Award, NIMH
1994-1999: First Award, NIMH
1993-1995: Basil O’Connor Scholar (March of Dimes Birth Defects Foundation), UCSD
1992-1995: Klingenstein Fellow in the Neurosciences, UCSD
1992-1994: Alfred P. Sloan Research Fellow, UCSD
1988-1991: Helen Hay Whitney Fellow, Whitehead Institute for Biomedical Research
1981-1988: Trainee, Medical Scientist Training Program (MSTP), Stanford University School of Medicine
Related Disease
Alzheimer’s Disease, Hydrocephalus, Multiple Sclerosis
Phenomena or Processes
Aneuploidy, Development and Differentiation, Development of Neuronal Circuits, G-Protein Coupled Receptors, Genome, Lipids, LPA, Mosaicism, S1P, Single Cell
Anatomical Systems and Sites
Brain, Nervous System
Lee MH, Siddoway B, Kaeser GE, Segota I, Rivera R, Romanow WJ, Liu CS, Park C, Kennedy G, Long T, Chun J
Nature 2018 Nov ;563(7733):639-645Groves A, Kihara Y, Jonnalagadda D, Rivera R, Kennedy G, Mayford M, Chun J
eNeuro 2018 Sep-Oct ;5(5):Groves A, Kihara Y, Jonnalagadda D, Rivera R, Kennedy G, Mayford M, Chun J
eNeuro 2018 Sep-Oct ;5(5):Dr. Blaho began her research career focused on how bioactive lipids contribute to the innate immune response against bacterial infection, characterizing roles for eicosanoids in the generation and resolution of Lyme arthritis pathology. The wild diversity of lipid species led Dr. Blaho to Weill Cornell Medical College in New York City to pursue postdoctoral training in the field of sphingolipids, particularly sphingosine 1-phosphate (S1P), and its receptors. Advancing to Instructor at Weill Cornell and later, Research Assistant Professor at Sanford Burnham Prebys, Dr. Blaho continued her research in lipid chaperones and receptor signaling, with an emphasis on cell-type differential effects on hematopoiesis and immunity in response to cell stressors. In August of 2019, Dr. Blaho joined the faculty at the Institute as an Assistant Professor in the Immunity and Pathogenesis program.
The immune system has the power to protect us from invading pathogens and cancer or to initiate a “self-destruct” sequence that consumes us with inflammation and autoimmunity. It is fascinating to me that a simple ubiquitous fat molecule like S1P can control the birth and destiny of immune cells.
2014-2016: Instructor, Weill Cornell Medicine, Pathology and Laboratory Medicine and Neuroscience
2009-2014: Post-doctoral training, Weill Cornell Medicine, Pathology and Laboratory Medicine
2007-2009: Post-doctoral training, University of Missouri, Columbia, Veterinary Pathobiology
2007: PhD, University of Missouri, Columbia, Molecular Microbiology and Immunology – BS
National Heart, Lung, and Blood Institute R01
American Heart Association Scientist Development Grant
2014-15: Leon Levy Neuroscience Foundation Grant
2015: Foundation LeDucq SphingoNet Young Investigator Grant
2009-12: National Cancer Institute Individual Ruth L. Kirschstein Post-doctoral Fellowship
2017: British Journal of Pharmacology Lecture: FASEB Summer Research Conference on Lysophospholipids and Related Mediators – from bench to clinic.
2014: Leon Levy Foundation Neuroscience Fellow
2010: Keystone Scholarship, Bioactive Lipids: Biochemistry and Diseases
2008: Keystone Scholarship, Eicosanoids and Other Mediators of Chronic Inflammation
2007: Young Investigator Award in Inflammation, Eicosanoid Research Foundation
2004: National Academy of Sciences Christine Mirzayan Policy Fellow, Institute of Medicine Board on Health Sciences Policy
Related Disease
Biochemistry, Immune Disorders, Inflammatory/Autoimmune Disease, Leukemia/Lymphoma, Molecular Biology, Multiple Sclerosis
Phenomena or Processes
Adaptive Immunity, Apoptosis and Cell Death, Cell Signaling, G-Protein Coupled Receptors, Hematopoiesis, Inflammation, Innate Immunity
Anatomical Systems and Sites
Hematopoietic System, Immune System and Inflammation, Vasculature
Research Models
Human Adult/Somatic Stem Cells, Mouse, Mouse Somatic Stem Cells, Primary Cells
Techniques and Technologies
Cell Biology, Cellular and Molecular Imaging, Confocal Microscopy, Fluorescence Microscopy, Gene Expression, Lipid Bilayers, Mass Spectrometry
The lipid sphingosine 1 phosphate (S1P) is found in high levels in the blood and lymph and is primarily carried by the protein ApoM, found on HDL. S1P can affect the cardiovascular, nervous, and immune systems via interaction with cell surface-expressed receptors, S1P1-5. My work is determining how changing S1P carrier or receptor expression and signaling can affect cells of the immune system, particularly in the bone marrow, and how this alters their ability to respond to stress or infection.
Blaho VA, Hla T
J Lipid Res 2014 Aug ;55(8):1596-608