## Abstract We stimulated differentiation of purified rat neural crest stem cells (NCSCs) into smooth muscle cells (SMCs) in culture, then subtracted NCSC sequences from SMC sequences to make a cDNA library specific for differentiating smooth muscle cells. Sequence analysis of the library shows tha
A quantitative description of active force generation in gastrointestinal smooth muscle
✍ Scribed by Viveka Gajendiran; Martin L. Buist
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Tongue
- English
- Weight
- 293 KB
- Volume
- 27
- Category
- Article
- ISSN
- 2040-7939
- DOI
- 10.1002/cnm.1419
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A mathematical model to describe the relationship between the intracellular Ca^2+^ concentration and active force production in a gastrointestinal (GI) smooth muscle cell (SMC) has been developed. Here the model has been constructed in terms of two modules, the first describing the activation of myosin light chain kinase (MLCK) through its interactions with calmodulin and Ca^2+^ ions, and the second consisting of a four state scheme describing myosin phosphorylation and cross‐bridge formation between actin and myosin. A prescribed Ca^2+^ transient, representing the dynamic changes in intracellular free Ca^2+^ that accompanies GI SMC excitation, was used as the input signal. Simulations demonstrated that at physiological Ca^2+^ levels, a 33% increase in peak Ca^2+^ concentration resulted in a 93% increase in myosin phosphorylation. This can possibly be attributed to the steep relationship between Ca^2+^ and MLCK activation over the normal Ca^2+^ range. The total number of cross‐bridges (sum of cycling cross‐bridges and latch‐bridges) was used to predict the active force generated in response to a phasic Ca^2+^ signal. The predicted forces were in qualitative agreement with experimental data from a canine antral smooth muscle strip. The development of this model represents a first step towards a greater understanding of the mechanisms that underlie GI motility. Copyright © 2010 John Wiley & Sons, Ltd.
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