The broad, long-term objectives of this research are to identify specific roles for matallothionein (MT) in mammalian species, particularly with respect to two important areas: (1) biochemical pathways for handling toxic heavy metals and (2) molecular responses to ionizing radiation an toxic metals. The proposed research focuses on the hypothesis that the MTs are highly inducible proteins that, throughout evolution, have provided protection against adverse environmental conditions, including those involving heavy metals (either excesses or deficiencies) and ionizing radiation. Because diet is the main source of human exposure to toxic metals in the environment, the proposed research will study the role of MT in the gastrointestinal (GI) absorption of toxic metals, in particular cadmium. Because of enhanced susceptibilities of fetal and neonatal tissues to toxic metals, the potentially important role of MT in cadmium transfer from dam to offspring will also be addressed. Finally, our extensive experience with ionizing radiation and cadmium will be applied to determine the role of MT in molecular responses to these carcinogenic agents. The approach uses the recently developed mouse strain in which both alleles of MT-1 and MT-II are inactivated (MT-knockout mice (Ma94).
The Specific Aims are to make use of MT-knockout (MT-KO) mice (Ma94) and MT-normal (MT-N) controls to determine the role of MT in; (1) Pathways of cadmium intestinal absorption and transfer from dam to offspring--pathways that are integral to defining target organ toxicities. (2) Molecular responses to radiation and cadmium, measured by changes in early gene expression and mutation frequency. Our guiding hypothesis is that MT-KO mice will (a) have altered metabolic pathways for transfering oral cadmium across the GI tract and for transfering cadmium from mother to offspring and (b) show increased sensitivity to radiation- and cadmium-induced gene changes that may be involved in carcinogenesis. Results of the proposed research will yield definitive insight into the function of MT in decreasing damage from toxic heavy metals and ionizing radiation -- two functions that appear to have been critical during evolution. Evaluation of MT's potential for decreasing transfer of Cd from mother to offspring will provide insight into protective pathways in women environmentally exposed to heavy metals during pregnancy and lactation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES007398-03
Application #
2654631
Study Section
Special Emphasis Panel (ZRG4-PHRA (01))
Project Start
1996-02-01
Project End
2000-01-31
Budget Start
1998-02-01
Budget End
2000-01-31
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Chicago
Department
Biology
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Bhattacharyya, Maryka H (2009) Cadmium osteotoxicity in experimental animals: mechanisms and relationship to human exposures. Toxicol Appl Pharmacol 238:258-65
Solaiman, D; Jonah, M M; Miyazaki, W et al. (2001) Increased metallothionein in mouse liver, kidneys, and duodenum during lactation. Toxicol Sci 60:184-92
Wilson, A K; Bhattacharyya, M H (1997) Effects of cadmium on bone: an in vivo model for the early response. Toxicol Appl Pharmacol 145:68-73