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      Transition From Phasic to Tonic Contractility in Airway Smooth Muscle After Birth: An Experimental and Computational Modeling Study

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          Abstract

          Fetal airway smooth muscle (ASM) exhibits phasic contractile behavior, which transitions to a more sustained “tonic” contraction after birth. The timing and underlying mechanisms of ASM transition from a phasic to a tonic contractile phenotype are yet to be established. We characterized phasic ASM contraction in preterm (128 day gestation), term (∼150 day gestation), 1–4 month, 1 yr, and adult sheep (5yr). Spontaneous phasic activity was measured in bronchial segments as amplitude, frequency, and intensity. The mechanism of phasic ASM contraction was investigated further with a computational model of ASM force development and lumen narrowing. The computational model comprised a two-dimensional cylindrical geometry of a network of contractile units and the activation of neighboring cells was dependent on the strength of coupling between cells. As expected, phasic contractions were most prominent in fetal airways and decreased with advancing age, to a level similar to the level in the 1–4 month lambs. Computational predictions demonstrated phasic contraction through the generation of a wave of activation events, the magnitude of which is determined by the number of active cells and the strength of cell–cell interactions. Decreases in phasic contraction with advancing age were simulated by reducing cell–cell coupling. Results show that phasic activity is suppressed rapidly after birth, then sustained at a lower intensity from the preweaning phase until adulthood in an ovine developmental model. Cell–cell coupling is proposed as a key determinant of phasic ASM contraction and if reduced could explain the observed maturational changes.

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          Most cited references47

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          A case for interstitial cells of Cajal as pacemakers and mediators of neurotransmission in the gastrointestinal tract.

          Electrical rhythmicity in gastrointestinal muscles has been studied for a century, but the pacemakers driving this phenomenon have been elusive. Anatomic studies suggest that interstitial cells of Cajal (ICC) may be pacemakers and conductors of electrical activity. ICC may also mediate neurotransmission from enteric neurons. Functional evaluations of ICC include the following. (1) Electrophysiology experiments on dissected muscle strips show that slow waves originate from specific sites. These pacemaker areas are populated by networks of ICC that make gap junctions with smooth muscle cells. Removal of pacemaker regions interferes with slow wave generation and propagation. (2) Chemicals that label ICC histochemically can damage ICC and abolish rhythmicity. (3) isolated ICC are spontaneously active, and several voltage-dependent ion channels, including a low-threshold Ca2+ conductance, are expressed. (4) ICC are innervated by enteric neurons, and they respond to neurotransmitters. ICC may produce nitric oxide and amplify inhibitory neurotransmission. (5) Some classes of ICC fall to develop in animals with mutations in c-kit or stem cell factor, the ligand for c-Kit receptors. Without ICC, electrical slow waves are absent. Many questions remain about the function of ICC, but modern technologies should now facilitate rapid progress toward determining the role of these cells in normal physiology and pathological conditions.
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            From mechanical force to RhoA activation.

            Throughout their lives, all cells constantly experience and respond to various mechanical forces. These frequently originate externally but can also arise internally as a result of the contractile actin cytoskeleton. Mechanical forces trigger multiple signaling pathways. Several converge and result in the activation of the GTPase RhoA. In this review, we focus on the pathways by which mechanical force leads to RhoA regulation, especially when force is transmitted via cell adhesion molecules that mediate either cell-matrix or cell-cell interactions. We discuss both the upstream signaling events that lead to activation of RhoA and the downstream consequences of this pathway. These include not only cytoskeletal reorganization and, in a positive feedback loop, increased myosin-generated contraction but also profound effects on gene expression and differentiation.
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              Smooth muscle cell calcium activation mechanisms.

              Smooth muscle cell (SMC) contraction is controlled by the Ca2+ and Rho kinase signalling pathways. While the SMC Rho kinase system seems to be reasonably constant, there is enormous variation with regard to the mechanisms responsible for generating Ca2+ signals. One way of dealing with this diversity is to consider how this system has been adapted to control different SMC functions. Phasic SMCs (vas deferens, uterus and bladder) rely on membrane depolarization to drive Ca2+ influx across the plasma membrane. This depolarization can be induced by neurotransmitters or through the operation of a membrane oscillator. Many tonic SMCs (vascular, airway and corpus cavernosum) are driven by a cytosolic Ca2+ oscillator that generates periodic pulses of Ca2+. A similar oscillator is present in pacemaker cells such as the interstitial cells of Cajal (ICCs) and atypical SMCs that control other tonic SMCs (gastrointestinal, urethra, ureter). The changes in membrane potential induced by these cytosolic oscillators does not drive contraction directly but it functions to couple together individual oscillators to provide the synchronization that is a characteristic feature of many tonic SMCs.
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                Author and article information

                Contributors
                Journal
                J Eng Sci Med Diagn Ther
                J Eng Sci Med Diagn Ther
                JESM
                Journal of Engineering and Science in Medical Diagnostics and Therapy
                American Society of Mechanical Engineers
                2572-7958
                2572-7966
                February 2019
                08 February 2019
                : 2
                : 1
                : 0110031-0110039
                Affiliations
                School of Human Sciences, The University of Western Australia, Crawley 6009, Western Australia, Australia; Telethon Kids Institute, The University of Western Australia, Perth 6009, Western Australia, Australia e-mail:  kimberley.wang@ 123456uwa.edu.au
                School of Human Sciences, The University of Western Australia, Crawley 6009, Western Australia, Australia
                School of Human Sciences, The University of Western Australia, Crawley 6009, Western Australia, Australia; Centre for Neonatal Research and Education, Medical School, The University of Western Australia, Perth 6009, Western Australia, Australia; King Edward Memorial Hospital, Subiaco 6008, Western Australia, Australia
                Department of Biomedical Engineering, Boston University, Boston, MA 02215
                School of Human Sciences, The University of Western Australia, Crawley 6009, Western Australia, Australia; Centre for Neonatal Research and Education, Medical School, The University of Western Australia, Perth 6009, Western Australia, Australia
                Author notes
                [1 ]Corresponding author.

                Manuscript received August 29, 2018; final manuscript received December 11, 2018; published online February 8, 2019. Assoc. Editor: Chun Seow.

                Article
                JESMDT-18-1041
                10.1115/1.4042312
                6467295
                31001605
                227f0f0a-823a-4777-a368-ad45a082b518
                Copyright © 2019 by ASME

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                : 29 August 2018
                : 11 December 2018
                Page count
                Pages: 9
                Funding
                Funded by: National Health and Medical Research Council 10.13039/501100000925
                Award ID: 1077691
                Funded by: National Institutes of Health 10.13039/100000002
                Award ID: HL-11745
                Categories
                Research Papers

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