mTOR Pathway Activation Following Sciatic Stimulation in Wild-Type and Desmin Knockout Mice

The 52 kDa intermediate filament protein desmin plays an important role in force transmission in skeletal muscle by connecting myofibrils at Z-lines and to the sarcolemma. Desmin content in muscle adapts to contractile activity and may be involved in cellular signaling mechanisms responsible for mus...

Full description

Bibliographic Details
Main Author: Nelson, Daniel S.
Format: Others
Published: BYU ScholarsArchive 2012
Subjects:
Online Access:https://scholarsarchive.byu.edu/etd/3503
https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4502&context=etd
id ndltd-BGMYU2-oai-scholarsarchive.byu.edu-etd-4502
record_format oai_dc
spelling ndltd-BGMYU2-oai-scholarsarchive.byu.edu-etd-45022019-05-16T03:17:54Z mTOR Pathway Activation Following Sciatic Stimulation in Wild-Type and Desmin Knockout Mice Nelson, Daniel S. The 52 kDa intermediate filament protein desmin plays an important role in force transmission in skeletal muscle by connecting myofibrils at Z-lines and to the sarcolemma. Desmin content in muscle adapts to contractile activity and may be involved in cellular signaling mechanisms responsible for muscle growth. Purpose: To compare signaling responses of the mTOR pathway in wild type (WT) vs desmin knock out (KO) mice. Methods: WT (n=12) and KO (n=12) mice were exposed to high frequency electric stimulation of the left hindlimb to elicit an acute response of the mTOR pathway. Non-stimulated right hindlimbs were used as a within animal control. Right and left TA and EDL muscles were dissected 30 min post-stimulation and examined for changes in mTOR, 4E-BP1 and p70S6K. Results: Relative to WT control samples, total mTOR and total 4E-BP1 content was higher in KO control samples. Electrical stimulation resulted in an increase p70S6K phosphorylation in WT and KO animals however there was no difference between the groups. 4E-BP1 phosphorylation was increased in WT but not KO following electrical stimulation. There was no change in mTOR phosphorylation in response to stimulation in WT or KO. Conclusion: The absence of desmin in skeletal muscle does not impair the phosphorylation of p70S6K demonstrating that a tensile load on the muscle will likely result in an increase in protein synthesis. Elevated levels of total mTOR and 4E-BP1 may imply an adaptation to increase sensitivity to growth stimuli in the muscle. 2012-12-13T08:00:00Z text application/pdf https://scholarsarchive.byu.edu/etd/3503 https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4502&context=etd http://lib.byu.edu/about/copyright/ All Theses and Dissertations BYU ScholarsArchive desmin knockout mTOR electrical stimulation 4E-BP1 p70S6k Exercise Science
collection NDLTD
format Others
sources NDLTD
topic desmin
knockout
mTOR
electrical stimulation
4E-BP1
p70S6k
Exercise Science
spellingShingle desmin
knockout
mTOR
electrical stimulation
4E-BP1
p70S6k
Exercise Science
Nelson, Daniel S.
mTOR Pathway Activation Following Sciatic Stimulation in Wild-Type and Desmin Knockout Mice
description The 52 kDa intermediate filament protein desmin plays an important role in force transmission in skeletal muscle by connecting myofibrils at Z-lines and to the sarcolemma. Desmin content in muscle adapts to contractile activity and may be involved in cellular signaling mechanisms responsible for muscle growth. Purpose: To compare signaling responses of the mTOR pathway in wild type (WT) vs desmin knock out (KO) mice. Methods: WT (n=12) and KO (n=12) mice were exposed to high frequency electric stimulation of the left hindlimb to elicit an acute response of the mTOR pathway. Non-stimulated right hindlimbs were used as a within animal control. Right and left TA and EDL muscles were dissected 30 min post-stimulation and examined for changes in mTOR, 4E-BP1 and p70S6K. Results: Relative to WT control samples, total mTOR and total 4E-BP1 content was higher in KO control samples. Electrical stimulation resulted in an increase p70S6K phosphorylation in WT and KO animals however there was no difference between the groups. 4E-BP1 phosphorylation was increased in WT but not KO following electrical stimulation. There was no change in mTOR phosphorylation in response to stimulation in WT or KO. Conclusion: The absence of desmin in skeletal muscle does not impair the phosphorylation of p70S6K demonstrating that a tensile load on the muscle will likely result in an increase in protein synthesis. Elevated levels of total mTOR and 4E-BP1 may imply an adaptation to increase sensitivity to growth stimuli in the muscle.
author Nelson, Daniel S.
author_facet Nelson, Daniel S.
author_sort Nelson, Daniel S.
title mTOR Pathway Activation Following Sciatic Stimulation in Wild-Type and Desmin Knockout Mice
title_short mTOR Pathway Activation Following Sciatic Stimulation in Wild-Type and Desmin Knockout Mice
title_full mTOR Pathway Activation Following Sciatic Stimulation in Wild-Type and Desmin Knockout Mice
title_fullStr mTOR Pathway Activation Following Sciatic Stimulation in Wild-Type and Desmin Knockout Mice
title_full_unstemmed mTOR Pathway Activation Following Sciatic Stimulation in Wild-Type and Desmin Knockout Mice
title_sort mtor pathway activation following sciatic stimulation in wild-type and desmin knockout mice
publisher BYU ScholarsArchive
publishDate 2012
url https://scholarsarchive.byu.edu/etd/3503
https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4502&context=etd
work_keys_str_mv AT nelsondaniels mtorpathwayactivationfollowingsciaticstimulationinwildtypeanddesminknockoutmice
_version_ 1719185242612301824