The combined central theme of this project is a combined Molecular/cellular effort to elucidate the fundamental processes regulated by extracellular molecules during limb morphogenetic tissue interactions. Five independent but related research component projects and a supporting core unit for monoclonal antibody preparation are proposed. These are: a) Project I: """"""""Extracellular Proteins in limb mesenchyme development"""""""" relates specifically to ectodermally-derived proteins and their potential role in the positional and overt cytodifferentiation of subpopulations of mesenchyme; b) Project II: """"""""Histone variants in limb development"""""""", seeks to identify the histones of active genes during differentiation of the major limb tissue types and any modifications following treatment with ectodermal proteins or endogenous, extracellular proteins; c) Project III: """"""""Muscle-specific ECM components in limb development"""""""", seeks to identify tissue specific molecules in the basal lamina of developing myogenically-committed mesenchyme and to define their functional roles: d) Project IV: """"""""Extracellular proteases in limb development: Cell Migration"""""""", will examine the role of extracellular proteases in the formation of somite-derived limb mesenchyme; e) Project V:""""""""Vascular influences on limb patterning"""""""", considers extracellular proteins derived from the other projects as well as other angiogenic factors in limb vasculogenesis and teratogenesis. The Core Unit is requested to expand our departmental monoclonal facility to accomodate the needs of all research proposed projects. Our enthusiasm for a program project effort stems from a collective desire of the applicants to extend their varied expertises and experiences in developmental/cellular phenomena to a specific tissue/organ level, like the limb system. This Program Project represents interdisciplinary approaches absolutely essential to elucidate mechanisms. The unique mix of talents and expertise in molecular/cellular biology, experimental embryology, clinical medicine and teratology, all predominately in the same academic department (Anatomy), should almost certainly yield a greater resolution to the problems and is certain to be synergistic in approach and in results.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
3P01HD020743-03S1
Application #
3096926
Study Section
Maternal and Child Health Research Committee (HDMC)
Project Start
1985-12-01
Project End
1989-11-30
Budget Start
1987-12-01
Budget End
1989-11-30
Support Year
3
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Medical College of Wisconsin
Department
Type
Schools of Medicine
DUNS #
073134603
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
Godfrey, E W; Gradall, K S (1998) Basal lamina molecules are concentrated in myogenic regions of the mouse limb bud. Anat Embryol (Berl) 198:481-6
Savage, M P; Fallon, J F (1995) FGF-2 mRNA and its antisense message are expressed in a developmentally specific manner in the chick limb bud and mesonephros. Dev Dyn 202:343-53
Ma, E; Morgan, R; Godfrey, E W (1995) Agrin mRNA variants are differentially regulated in developing chick embryo spinal cord and sensory ganglia. J Neurobiol 26:585-97
Cohen, M W; Jacobson, C; Godfrey, E W et al. (1995) Distribution of alpha-dystroglycan during embryonic nerve-muscle synaptogenesis. J Cell Biol 129:1093-101
Smith, S M; Kirstein, I J; Wang, Z S et al. (1995) Differential expression of retinoic acid receptor-beta isoforms during chick limb ontogeny. Dev Dyn 202:54-66
Lopez-Martinez, A; Chang, D T; Chiang, C et al. (1995) Limb-patterning activity and restricted posterior localization of the amino-terminal product of Sonic hedgehog cleavage. Curr Biol 5:791-6
Krug, E L; Rezaee, M; Isokawa, K et al. (1995) Transformation of cardiac endothelium into cushion mesenchyme is dependent on ES/130: temporal, spatial, and functional studies in the early chick embryo. Cell Mol Biol Res 41:263-77
Ros, M A; Lyons, G E; Mackem, S et al. (1994) Recombinant limbs as a model to study homeobox gene regulation during limb development. Dev Biol 166:59-72
Borman, W H; Urlakis Jr, K J; Yorde, D E (1994) Analysis of the in vivo myogenic status of chick somites by desmin expression in vitro. Dev Dyn 199:268-79
Ma, E; Morgan, R; Godfrey, E W (1994) Distribution of agrin mRNAs in the chick embryo nervous system. J Neurosci 14:2943-52

Showing the most recent 10 out of 42 publications