𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Dependence of alignment direction on magnitude of strain in esophageal smooth muscle cells

✍ Scribed by A.C. Ritchie; S. Wijaya; W.F. Ong; S.P. Zhong; K.S. Chian


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
652 KB
Volume
102
Category
Article
ISSN
0006-3592

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The response of cells in vitro to mechanical forces has been the subject of much research using devices to exert controlled mechanical stimulation on cultured cells or isolated tissue. In this study, esophageal smooth muscle cells were seeded on flexible polyurethane membranes to form a confluent cell layer. The cells were then subjected to uniform cyclic stretch of varying magnitudes at a frequency of approximately five cycles per minute in a custom made mechatronic bioreactor, providing similar strains experienced in the in vivo mechanical environment of the esophagus. The results show that the orientation response is dependent on the magnitude of cyclic stretch applied. Smooth muscle cells showed parallel alignment to the force direction at low cyclic strains (2%) compared to the hill‐valley morphology of static controls. At higher strains (5% and 10% magnitude), the cells exhibited a consistent alignment perpendicular to the strain. To our knowledge, this is the first time that the alignment direction's dependence on strain magnitude has been demonstrated. MTS analysis indicated that cell metabolism was reduced when mechanical strain was applied, and proliferation was inhibited by mechanical strain. Protein expression indicates a decrease in smooth muscle α‐actin, indicative of changes in cell phenotype, an increase in vimentin, which is associated with increased cell motility, and an increase in desmin, indicating differentiation in stimulated cells. Biotechnol. Bioeng. 2009;102: 1703–1711. Β© 2008 Wiley Periodicals, Inc.


πŸ“œ SIMILAR VOLUMES


Strain activation of bovine aortic smoot
✍ Ira Mills; C. Richard Cohen; Khurram Kamal; Guangdi Li; Tae Shin; Wei Du; Bauer πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 211 KB πŸ‘ 2 views

Smooth muscle cell (SMC) phenotype can be altered by physical forces as demonstrated by cyclic strain-induced changes in proliferation, orientation, and secretion of macromolecules. However, the magnitude of strain required and the intracellular coupling pathways remain ill defined. To examine the s

In vitro ovulation of hamster oocytes de
✍ Talbot, Prudence ;Chacon, R. S. πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 English βš– 476 KB

## Abstract Smooth muscle cells (SMC) of the hamster follicle contract prior to ovulation, and their contraction produces a V‐shaped constriction in the base of the follicle. We have determined when basal constrictions first appear in follicles removed from females at various preovulatory times by

Mechanical strain induces a persistent u
✍ Matheau A. Julien; Carolyn A. Haller; Peiyi Wang; Jing Wen; Elliot L. Chaikof πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 181 KB

## Abstract Syndecan‐1 belongs to a family of transmembrane proteoglycans, acts as a coreceptor for growth factor binding, as well as cell–matrix and cell–cell interactions, and is induced in smooth muscle cells (SMCs) following balloon catheter injury. In this report, we investigated syndecan‐1 ex

Involvement of S6 kinase and p38 mitogen
✍ Wei Li; Quanhai Chen; Ira Mills; Bauer E. Sumpio πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 253 KB πŸ‘ 2 views

## Abstract Bovine aortic smooth muscle cell (SMC) phenotype can be altered by physical forces. This has been demonstrated by cyclic strain‐induced changes in proliferation and alignment. However, the intracellular coupling pathways remain ill defined. In the present study, we examined whether the

Influence of channel width on alignment
✍ John D. Glawe; Jason B. Hill; David K. Mills; Michael J. McShane πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 329 KB

## Abstract Engineered smooth muscle tissue requires ordered configurations of cells to reproduce native function, and microtechnology offers possibilities for physically and chemically controlling cell organization with high spatial resolution. In this work, poly(dimethylsiloxane) microchannel sca