Identification of a novel stretch-responsive skeletal muscle gene (smpx)

Kemp, T.J., Sadusky, T.J., Simon, M., Brown, R.A., Eastwood, M., Sassoon, D.A. and Coulton, G.R. 2001. Identification of a novel stretch-responsive skeletal muscle gene (smpx). Genomics. 72 (3), pp. 260-271. https://doi.org/10.1006/geno.2000.6461

TitleIdentification of a novel stretch-responsive skeletal muscle gene (smpx)
AuthorsKemp, T.J., Sadusky, T.J., Simon, M., Brown, R.A., Eastwood, M., Sassoon, D.A. and Coulton, G.R.
Abstract

Skeletal muscle is able to respond to a range of stimuli, including stretch and increased load, by increasing in diameter and length in the absence of myofiber division. This type of cellular growth (hypertrophy) is a highly complex process involving division of muscle precursor cells (myoblasts) and their fusion to existing muscle fibers as well as increased protein synthesis and decreased protein degradation. Underlying the alterations in protein levels are increases in a range of specific mRNAs including those coding for structural proteins and proteins that regulate the hypertrophic process. Seven days of passive stretch in vivo of tibialis anterior (TA) muscle has been shown to elicit muscle hypertrophy. We have identified a cDNA corresponding to an mRNA that exhibits increased expression in response to 7 days of passive stretch imposed on TA muscles in vivo. This 944-bp novel murine transcript is expressed primarily in cardiac and skeletal muscle and to a lesser extent in brain. Translation of the transcript revealed an open reading frame of 85 amino acids encoding a nuclear localization signal and two overlapping casein kinase II phosphorylation sites. This gene has been called “small muscle protein (X chromosome)” (Smpx; HGMW-approved human gene symbol SMPX) and we hypothesize that it plays a role in skeletal muscle hypertrophy.

JournalGenomics
Journal citation72 (3), pp. 260-271
ISSN0888-7543
Year15 Mar 2001
Digital Object Identifier (DOI)https://doi.org/10.1006/geno.2000.6461
Publication dates
Published15 Mar 2001

Related outputs

Periostin modulates myofibroblast differentiation during full-thickness cutaneous wound repair
Elliott, C.G., Wang, J., Guo, X., Xu, S.W., Eastwood, M., Guan, J., Leask, A., Conway, S.J., Hamilton, D.W. and Shi-Wen, X. 2012. Periostin modulates myofibroblast differentiation during full-thickness cutaneous wound repair. Journal of Cell Science. 125 (1), pp. 121-132. https://doi.org/10.1242/jcs.087841

In vitro mesenchymal stem cell differentiation after mechanical stimulation
Sarraf, C., Otto, W.R. and Eastwood, M. 2011. In vitro mesenchymal stem cell differentiation after mechanical stimulation. Cell Proliferation. 44 (1), pp. 99-108. https://doi.org/10.1111/j.1365-2184.2010.00740.x

Thrombospondin 1 is a key mediator of transforming growth factor β-mediated cell contractility in systemic sclerosis via a mitogen-activated protein kinase kinase (MEK)/extracellular signal-regulated kinase (ERK)-dependent mechanism
Chen, Y., Leask, A., Abraham, D.J., Kennedy, L., Shi-Wen, X., Denton, C.P., Black, C.M., Verjee, L.S. and Eastwood, M. 2011. Thrombospondin 1 is a key mediator of transforming growth factor β-mediated cell contractility in systemic sclerosis via a mitogen-activated protein kinase kinase (MEK)/extracellular signal-regulated kinase (ERK)-dependent mechanism. Fibrogenesis and tissue repair. 4 (9). https://doi.org/10.1186/1755-1536-4-9

Expression of integrin β1 by fibroblasts is required for tissue repair in vivo
Liu, S., Shi-Wen, X., Blumbach, K., Eastwood, M., Denton, C.P., Eckes, B., Krieg, T., Abraham, D.J. and Leask, A. 2010. Expression of integrin β1 by fibroblasts is required for tissue repair in vivo. Journal of Cell Science. 123 (21), pp. 3674-3682. https://doi.org/10.1242/jcs.070672

Post-transcriptional regulation of alpha-smooth muscle actin determines the contractile phenotype of Dupuytren's nodular cells
Verjee, L.S., Midwood, K., Davidson, D., Eastwood, M. and Nanchahal, J. 2010. Post-transcriptional regulation of alpha-smooth muscle actin determines the contractile phenotype of Dupuytren's nodular cells. Journal of Cellular Physiology. 224 (3), pp. 681-690. https://doi.org/10.1002/jcp.22167

Rosiglitazone alleviates the persistent fibrotic phenotype of lesional skin scleroderma fibroblasts
Shi-Wen, X., Eastwood, M., Stratton, R.J., Denton, C.P., Leask, A. and Abraham, D.J. 2010. Rosiglitazone alleviates the persistent fibrotic phenotype of lesional skin scleroderma fibroblasts. Rheumatology. 49 (2), pp. 259-263. https://doi.org/10.1093/rheumatology/kep371

Rac inhibition reverses the phenotype of fibrotic fibroblasts
Shi-Wen, X., Liu, S., Eastwood, M., Sonnylal, S., Denton, C.P., Abraham, D.J. and Leask, A. 2009. Rac inhibition reverses the phenotype of fibrotic fibroblasts. PLoS ONE. 4 (10) e7438. https://doi.org/10.1371/journal.pone.0007438

Requirement of transforming growth factor β–activated kinase 1 for transforming growth factor β–induced -smooth muscle actin expression and extracellular matrix contraction in fibroblasts
Shi-Wen, X., Parapuram, S.K., Pala, D., Chen, Y., Carter, D.E., Eastwood, M., Denton, C.P., Abraham, D.J. and Leask, A. 2009. Requirement of transforming growth factor β–activated kinase 1 for transforming growth factor β–induced -smooth muscle actin expression and extracellular matrix contraction in fibroblasts. Arthritis & Rheumatism. 60 (1), pp. 234-241. https://doi.org/10.1002/art.24223

Inducible lineage-specific deletion of TβRII in fibroblasts defines a pivotal regulatory role during adult skin wound healing
Denton, C.P., Khan, K., Hoyles, R.K., Shiwen, X., Leoni, P., Chen, Y., Eastwood, M. and Abraham, D.J. 2009. Inducible lineage-specific deletion of TβRII in fibroblasts defines a pivotal regulatory role during adult skin wound healing. Journal of Investigative Dermatology. 129 (1), pp. 194-204. https://doi.org/10.1038/jid.2008.171

Heparan sulfate-dependent ERK activation contributes to the overexpression of fibrotic proteins and enhanced contraction by scleroderma fibroblasts
Chen, Y., Leask, A., Abraham, D.J., Pala, D., Shiwen, X., Khan, K., Liu, S., Carter, D.E., Wilcox-Adelman, S., Goetinck, P.F., Denton, C.P., Black, C.M., Pitsillides, A.A., Sarraf, C. and Eastwood, M. 2008. Heparan sulfate-dependent ERK activation contributes to the overexpression of fibrotic proteins and enhanced contraction by scleroderma fibroblasts. Arthritis & Rheumatism. 58 (2), pp. 577-585. https://doi.org/10.1002/art.23146

Dynamic protrusive cell behaviour generates force and drives early matrix contraction by fibroblasts
Dahlmann-Noor, A.H., Martin-Martin, B., Eastwood, M., Khaw, P.T. and Bailly, M. 2007. Dynamic protrusive cell behaviour generates force and drives early matrix contraction by fibroblasts. Experimental Cell Research. 313 (20), pp. 4158-4169. https://doi.org/10.1016/j.yexcr.2007.07.040

Force generation of different human cardiac valve interstitial cells: relevance to individual valve function and tissue engineering
Smith, S., Taylor, P.M., Chester, A.H., Allen, S.P., Dreger, S.A., Eastwood, M. and Yacoub, M.H. 2007. Force generation of different human cardiac valve interstitial cells: relevance to individual valve function and tissue engineering. Journal of Heart Valve Disease. 16 (4), pp. 440-446.

FAK Is Required for TGFβ-induced JNK Phosphorylation in Fibroblasts: Implications for Acquisition of a Matrix-remodeling Phenotype
Shangxi, L., Shi-Wen, X., Kennedy, L., Pala, D., Chen, Y., Eastwood, M., Carter, D.E., Black, C.M., Abraham, D.J. and Leask, A. 2007. FAK Is Required for TGFβ-induced JNK Phosphorylation in Fibroblasts: Implications for Acquisition of a Matrix-remodeling Phenotype. Molecular Biology of the Cell. 18 (6), pp. 2169-2178. https://doi.org/10.1091/mbc.E06-12-1121

CCN2 is necessary for the function of mouse embryonic fibroblasts
Kennedy, L., Liu, S., Shi-Wen, X., Chen, Y., Eastwood, M., Carter, D.E., Lyon, K.M., Black, C.M., Abraham, D.J. and Leask, A. 2007. CCN2 is necessary for the function of mouse embryonic fibroblasts. Experimental Cell Research. 313 (5), pp. 952-964. https://doi.org/10.1016/j.yexcr.2006.12.006

Contribution of activin receptor-like kinase 5 (transforming growth factor beta receptor type I) signaling to the fibrotic phenotype of scleroderma fibroblasts
Chen, Y., Shi-Wen, X., Eastwood, M., Black, C.M., Denton, C.P., Leask, A. and Abraham, D.J. 2006. Contribution of activin receptor-like kinase 5 (transforming growth factor beta receptor type I) signaling to the fibrotic phenotype of scleroderma fibroblasts. Arthritis & Rheumatism. 54 (4), pp. 1309-1316. https://doi.org/10.1002/art.21725

Matrix contraction by dermal fibroblasts requires transforming growth Factor-ß /activin-linked kinase 5, heparan sulfate-containing proteoglycans, and MEK/ERK: insights into pathological scarring in chronic fibrotic disease
Chen, Y., Shi-Wen, X., van Beek, J., Kennedy, L., McLeod, M., Renzoni, E.A., Bou-Gharios, G., Wilcox-Adelman, S., Goetinck, P.F., Eastwood, M., Black, C.M., Abraham, D.J. and Leask, A. 2005. Matrix contraction by dermal fibroblasts requires transforming growth Factor-ß /activin-linked kinase 5, heparan sulfate-containing proteoglycans, and MEK/ERK: insights into pathological scarring in chronic fibrotic disease. American Journal of Pathology. 167 (6), pp. 1699-1711.

Cell proliferation rates in an artificial tissue-engineered environment
Sarraf, C., Harris, A.B., McCulloch, A.D. and Eastwood, M. 2005. Cell proliferation rates in an artificial tissue-engineered environment. Cell Proliferation. 38 (4), pp. 215-221. https://doi.org/10.1111/j.1365-2184.2005.00347.x

Investigating the mechanical shear-plane between core and sheath elements of peripheral nerves
Georgeu, G.A., Walbeehm, E.T., Tillett, R.L., Afoke, A., Brown, R.A. and Phillips, J.B. 2005. Investigating the mechanical shear-plane between core and sheath elements of peripheral nerves. Cell and Tissue Research. 320 (2), pp. 229-234. https://doi.org/10.1007/s00441-004-1031-2

Activation of Key Profibrotic Mechanisms in Transgenic Fibroblasts Expressing Kinase-deficient Type II Transforming Growth Factor beta-receptor (T beta RII delta k)
Denton, C.P., Lindahl, G.E., Khan, K., Shiwen, X., Ong, V.H., Gaspar, N.J., Lazaridis, K., Edwards, D.R., Leask, A., Eastwood, M., Leoni, P., Renzoni, E.A., Bou-Gharios, G., Abraham, D.J. and Black, C.M. 2005. Activation of Key Profibrotic Mechanisms in Transgenic Fibroblasts Expressing Kinase-deficient Type II Transforming Growth Factor beta-receptor (T beta RII delta k). Journal of Biological Chemistry. 280 (16), pp. 16053-16065. https://doi.org/10.1074/jbc.M413134200

Stem cells, tissue engineering and the mechanical environment
Sarraf, C. and Eastwood, M. 2005. Stem cells, tissue engineering and the mechanical environment. in: Ashammakhi, N.A. and Reis, R.L. (ed.) Topics in tissue engineering Biomaterials and tissue engineering group.

Investigating mechanical behaviour at a core-sheath interface in peripheral nerve
Tillett, R.L., Afoke, A., Hall, S.M., Brown, R.A. and Phillips, J.B. 2004. Investigating mechanical behaviour at a core-sheath interface in peripheral nerve. Journal of the Peripheral Nervous System. 9 (4), pp. 255-262. https://doi.org/10.1111/j.1085-9489.2004.09411.x

Endothelin-1 promotes myofibroblast induction through the ETA receptor via a rac/phosphoinositide 3-kinase/akt-dependent pathway and is essential for the enhanced contractile phenotype of fibrotic fibroblasts
Shi-Wen, X., Chen, Y., Denton, C.P., Eastwood, M., Renzoni, E.A., Bou-Gharios, G., Pearson, J., Dashwood, M., du Bois, R., Black, C.M., Leask, A. and Abraham, D.J. 2004. Endothelin-1 promotes myofibroblast induction through the ETA receptor via a rac/phosphoinositide 3-kinase/akt-dependent pathway and is essential for the enhanced contractile phenotype of fibrotic fibroblasts. Molecular Biology of the Cell. 15 (6), pp. 2707-2719. https://doi.org/10.1091/mbc.E03-12-0902

Peripheral nerves in the rat exhibit localized heterogeneity of tensile properties during limb movement
Phillips, J.B., Smit, X., De Zoysa, N., Afoke, A. and Brown, R.A. 2004. Peripheral nerves in the rat exhibit localized heterogeneity of tensile properties during limb movement. Journal of Physiology. 557 (3), pp. 879-887. https://doi.org/10.1113/jphysiol.2004.061804

Mechanical functioning of peripheral nerves: linkage with the "mushrooming" effect
Walbeehm, E.T., Afoke, A., Wit, T., Holman, F., Hovius, S.E.R. and Brown, R.A. 2004. Mechanical functioning of peripheral nerves: linkage with the "mushrooming" effect. Cell and Tissue Research. 316 (1), pp. 115-121. https://doi.org/10.1007/s00441-004-0867-9

New multi-cue bioreactor for tissue engineering of tubular cardiovascular samples under physiological conditions
McCulloch, A.D., Harris, A.B., Sarraf, C. and Eastwood, M. 2004. New multi-cue bioreactor for tissue engineering of tubular cardiovascular samples under physiological conditions. Tissue Engineering. 10 (3/4), pp. 565-573.

Heart valve and arterial tissue engineering
Sarraf, C., Harris, A.B., McCulloch, A.D. and Eastwood, M. 2003. Heart valve and arterial tissue engineering. Cell Proliferation. 36 (5), pp. 241-254. https://doi.org/10.1046/j.1365-2184.2003.00281.x

Evidence for sequential utilization of fibronectin, vitronectin, and collagen during fibroblast-mediated collagen contraction
Sethi, K.K., Yannas, I.V., Mudera, V., Eastwood, M., McFarland, C. and Brown, R.A. 2002. Evidence for sequential utilization of fibronectin, vitronectin, and collagen during fibroblast-mediated collagen contraction. Wound Repair and Regeneration. 10 (6), pp. 397 -408. https://doi.org/10.1046/j.1524-475X.2002.10609.x

Enhanced fibroblast contraction of 3D collagen lattices and integrin expression by TGF-β1 and -β: mechanoregulatory growth factors?
Brown, R.A., Sethi, K.K., Gwanmesia, I., Raemdonck, D., Eastwood, M. and Mudera, V. 2002. Enhanced fibroblast contraction of 3D collagen lattices and integrin expression by TGF-β1 and -β: mechanoregulatory growth factors? Experimental Cell Research. 274 (2), pp. 310-322. https://doi.org/10.1006/excr.2002.5471

Tissue engineering of biological cardiovascular system surrogates
Sarraf, C., Harris, A.B., McCulloch, A.D. and Eastwood, M. 2002. Tissue engineering of biological cardiovascular system surrogates. Heart, Lung & Circulation. 11 (3), pp. 142-150. https://doi.org/10.1046/j.1444-2892.2002.00150.x

Permalink - https://westminsterresearch.westminster.ac.uk/item/93zw9/identification-of-a-novel-stretch-responsive-skeletal-muscle-gene-smpx


Share this

Usage statistics

103 total views
0 total downloads
These values cover views and downloads from WestminsterResearch and are for the period from September 2nd 2018, when this repository was created.