The purpose of this project will be to examine the structural organization of smooth muscle and to determine how this organization changes as contraction takes place. This study will provide important new information about how the contractile apparatus is arranged in smooth muscle, how it is integrated into the cytoplasmic matrix, and how forces are transmitted within smooth muscle cells and between the cells that make up the whole tissue. Contractile proteins and various proteins associated with dense bodies, which are the attachment sites for actin filaments in smooth muscle, will be identified, studied biochemically, and labeled with fluorescent antibodies. The way these proteins are organized into structural elements in the cell and their relationship to one another and the dense body structures will then be studied in several ways. The protein composition of isolated dense body structures and the filaments associated with them will be examined biochemically and antibodies will be made to these proteins. The phase contrast and fluorescence microscope along with digital imaging and image processing techniques will then be used to examine the location and movement of specific structures labeled with antibodies in skinned isolated smooth muscle cells during contraction. To do this, digital images, collected at fixed time intervals during shortening, will be analyzed quantitatively to provide specific information about the rate and direction of movement of structures in contracting cells and how various elements move with respect to one another. Both whole cell and localized contraction will be examined in this way. The experiments will provide an overall picture of the smooth muscle cell during contraction and specific information about the relationship of various structures to one another. These results will provide new information about the organization of smooth muscle that can be used as a knowledge base for understanding healthy and diseased smooth muscle and its relationship to other muscle and tissue types.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
1R29AR039678-01A1
Application #
3457143
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1989-09-30
Project End
1994-08-31
Budget Start
1989-09-30
Budget End
1990-08-31
Support Year
1
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Type
Schools of Medicine
DUNS #
660735098
City
Worcester
State
MA
Country
United States
Zip Code
01655
Scott-Woo, G C; Walsh, M P; Ikebe, M et al. (1998) Identification and localization of caldesmon in cardiac muscle. Biochem J 334 ( Pt 1):161-70
Kargacin, M E; Kargacin, G J (1996) The sarcoplasmic reticulum calcium pump is functionally altered in dystrophic muscle. Biochim Biophys Acta 1290:4-8
Kargacin, M E; Kargacin, G J (1995) Direct measurement of Ca2+ uptake and release by the sarcoplasmic reticulum of saponin permeabilized isolated smooth muscle cells. J Gen Physiol 106:467-84
Kargacin, G J (1994) Calcium signaling in restricted diffusion spaces. Biophys J 67:262-72
Kargacin, M E; Kargacin, G J (1994) Methods for determining cardiac sarcoplasmic reticulum Ca2+ pump kinetics from fura 2 measurements. Am J Physiol 267:C1145-51
Carmichael, J D; Winder, S J; Walsh, M P et al. (1994) Calponin and smooth muscle regulation. Can J Physiol Pharmacol 72:1415-9
Walsh, M P; Carmichael, J D; Kargacin, G J (1993) Characterization and confocal imaging of calponin in gastrointestinal smooth muscle. Am J Physiol 265:C1371-8
Kargacin, G; Fay, F S (1991) Ca2+ movement in smooth muscle cells studied with one- and two-dimensional diffusion models. Biophys J 60:1088-100
Kargacin, G J; Ikebe, M; Fay, F S (1990) Peptide modulators of myosin light chain kinase affect smooth muscle cell contraction. Am J Physiol 259:C315-24