The Bioengineering for Toxicology core was created to facilitate the development of new experimental tools and analysis methods relevant to the scientific foci of the two other Research Cores with an initial emphasis on activities in the Mutation and Cancer Research Core.
Our aim i s to develop a range of approaches that span the molecular-cellular-systems length scales to solve problems in toxicology and environmental health. The experimental tools range from tissue-engineered physiological bioreactors that bridge the gap between cell culture, animal models, and humans; and multiphoton imaging methods that allow in situ quantification of events such as single cell apoptosis and DNA recombination by scanning large populations of cells in tissues and tissue models. Analytical methods include statistical (Bayesian) and deterministic models of signal transduction networks and computational models of protein interactions in the context of different cell compartments.
The Specific Aims of this Core are: (1) To provide a mechanism for bringing new bioengineering experimental and analytical methods into the study of Toxicology and Environmental Health problems.(2) To link new experimental tools and new analytical methods to describe molecular-to-systems level events in DNA damage, repair, mutagenesis and carcinogenesis induced by environmental agents. (3) To further the development of research projects and programs that address the linkages between exposure to environmental and endogenous agents, genetic change and cancer and other diseases with an emphasis on building better models of the human condition. (4) To promote interaction among the Bioengineering for Toxicology Research Core members, and to promote interactions between members of this and the other two Research Cores with the goal of creating new research projects and programs. (5) To promote the development and acquisition of new technologies in the Center Facilities Cores that will facilitate studies in the Bioengineering for Toxicology Core. (6) To disseminate engineered systems and tools developed at MIT to a broader community of toxicology and environmental health researchers.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES002109-27
Application #
7530264
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
27
Fiscal Year
2006
Total Cost
$6,137
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Viswanathan, Srinivas R; Nogueira, Marina F; Buss, Colin G et al. (2018) Genome-scale analysis identifies paralog lethality as a vulnerability of chromosome 1p loss in cancer. Nat Genet 50:937-943
Winn, Caroline Bodi; Artim, Stephen C; Jamiel, Morgan S et al. (2018) Lung Lobe Torsion in an Adult Male Common Marmoset (Callithrix jacchus). Comp Med 68:314-318
Co, Julia Y; Cárcamo-Oyarce, Gerardo; Billings, Nicole et al. (2018) Mucins trigger dispersal of Pseudomonas aeruginosa biofilms. NPJ Biofilms Microbiomes 4:23
Keegan, Caroline; Krutzik, Stephan; Schenk, Mirjam et al. (2018) Mycobacterium tuberculosis Transfer RNA Induces IL-12p70 via Synergistic Activation of Pattern Recognition Receptors within a Cell Network. J Immunol 200:3244-3258
DiChiara, Andrew S; Li, Rasia C; Suen, Patreece H et al. (2018) A cysteine-based molecular code informs collagen C-propeptide assembly. Nat Commun 9:4206
Caron, Tyler J; Artim, Stephen C; Israelsen, William J et al. (2018) Cutaneous Dermatophilosis in a Meadow Jumping Mouse (Zapus hudsonius). Comp Med 68:25-30
Phillips, Angela M; Doud, Michael B; Gonzalez, Luna O et al. (2018) Enhanced ER proteostasis and temperature differentially impact the mutational tolerance of influenza hemagglutinin. Elife 7:
Wang, Xin; Garcia, Carlos T; Gong, Guanyu et al. (2018) Automated Online Solid-Phase Derivatization for Sensitive Quantification of Endogenous S-Nitrosoglutathione and Rapid Capture of Other Low-Molecular-Mass S-Nitrosothiols. Anal Chem 90:1967-1975
Moore, Christopher L; Papa 3rd, Louis J; Shoulders, Matthew D (2018) A Processive Protein Chimera Introduces Mutations across Defined DNA Regions In Vivo. J Am Chem Soc 140:11560-11564
Chan, Cheryl; Pham, Phuong; Dedon, Peter C et al. (2018) Lifestyle modifications: coordinating the tRNA epitranscriptome with codon bias to adapt translation during stress responses. Genome Biol 19:228

Showing the most recent 10 out of 970 publications