The overarching aim of the Center is to provide a systems-level understanding for cellular decision-making focusing on the interrelated processes of cell proliferation, migration, and differentiation. Particularly, we will be focusing on how to develop and validate models that range from molecular single cell mechanisms to collective cell behavior. The center includes a research component with three synergistic projects, cores that will enrich systems biology research in Stanford, as well as an education component focusing on training graduate student and postdoctoral fellows in this emerging new field. We will also have an outreach effort to disseminate data sets and models and to invite researchers to participate in summer courses as well as to train in systems biology in Stanford. In the proposed research, we will focus on Collective Cell Proliferation by focusing on Xenopus laevis embryos and on primary human umbilical vein endothelial cells using novel biosensors developed in the participating laboratories. Our effort to understand Collective Cell Migration wil focus on mechanical models for collective migration based on novel insights into the propagation of force in 2-dimensional cell sheets. In our third effort to understand Collective Cel Differentiation we will be focusing on learning the rules by which cells collectively transition from proliferative to differentiated states using human induced pluripotent stem (IPS) cells, granule neuron precursors (GNP), adipocytes, and drosophila wing epithelial cells as models. Since neighboring cells tend to differentiate in a correlated fashion, we will seek to understand how cells coordinate differentiation by testing whether secreted factors and direct cell contact contribute to collective differentiation decisions. These research efforts will be augmented by the development of new perturbation and biosensor technologies that will enable us to validate models for these processes. The investigated biological projects share common regulatory designs, adding significant synergies that will enhance the change that significant new advances will be made in the proposed Center.

Public Health Relevance

The proposed work will elucidate fundamental regulatory mechanisms how cells divide, move and differentiate. These processes are critical in cancer, neurodegeneration and in many other diseases. Insights into the regulation of these processes may lead, with a longer term time horizon, to new types of therapies for these diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center (P50)
Project #
5P50GM107615-05
Application #
9307912
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Nie, Zhongzhen
Project Start
2013-09-30
Project End
2018-06-30
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
5
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Stanford University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94304
Zhou, Xin X; Zou, Xinzhi; Chung, Hokyung K et al. (2018) A Single-Chain Photoswitchable CRISPR-Cas9 Architecture for Light-Inducible Gene Editing and Transcription. ACS Chem Biol 13:443-448
Vladar, Eszter K; Stratton, Miranda B; Saal, Maxwell L et al. (2018) Cyclin-dependent kinase control of motile ciliogenesis. Elife 7:
Jacobson, Amanda; Lam, Lilian; Rajendram, Manohary et al. (2018) A Gut Commensal-Produced Metabolite Mediates Colonization Resistance to Salmonella Infection. Cell Host Microbe 24:296-307.e7
Daigle, Tanya L; Madisen, Linda; Hage, Travis A et al. (2018) A Suite of Transgenic Driver and Reporter Mouse Lines with Enhanced Brain-Cell-Type Targeting and Functionality. Cell 174:465-480.e22
Tropini, Carolina; Moss, Eli Lin; Merrill, Bryan Douglas et al. (2018) Transient Osmotic Perturbation Causes Long-Term Alteration to the Gut Microbiota. Cell 173:1742-1754.e17
Bell, Jason C; Jukam, David; Teran, Nicole A et al. (2018) Chromatin-associated RNA sequencing (ChAR-seq) maps genome-wide RNA-to-DNA contacts. Elife 7:
Rodriguez-Rivera, Frances P; Zhou, Xiaoxue; Theriot, Julie A et al. (2018) Acute Modulation of Mycobacterial Cell Envelope Biogenesis by Front-Line Tuberculosis Drugs. Angew Chem Int Ed Engl 57:5267-5272
Colavin, Alexandre; Shi, Handuo; Huang, Kerwyn Casey (2018) RodZ modulates geometric localization of the bacterial actin MreB to regulate cell shape. Nat Commun 9:1280
Odermatt, Pascal D; Arjes, Heidi A; Chang, Fred et al. (2018) Who's Your DadA? d-Alanine Levels Regulate Bacterial Stiffness. MBio 9:
Rojas, Enrique R; Huang, Kerwyn Casey (2018) Regulation of microbial growth by turgor pressure. Curr Opin Microbiol 42:62-70

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