LRP receptors in chondrocytes are modulated by simulated microgravity and cyclic hydrostatic pressure.

Mechanical loading is essential for the maintenance of musculoskeletal homeostasis. Cartilage has been demonstrated to be highly mechanoresponsive, but the mechanisms by which chondrocytes respond to mechanical stimuli are not clearly understood. The goal of the study was to determine how LRP4, LRP5...

Full description

Bibliographic Details
Main Authors: Rachel C Nordberg, Liliana F Mellor, Andrew R Krause, Henry J Donahue, Elizabeth G Loboa
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0223245
_version_ 1818725663307202560
author Rachel C Nordberg
Liliana F Mellor
Andrew R Krause
Henry J Donahue
Elizabeth G Loboa
author_facet Rachel C Nordberg
Liliana F Mellor
Andrew R Krause
Henry J Donahue
Elizabeth G Loboa
author_sort Rachel C Nordberg
collection DOAJ
description Mechanical loading is essential for the maintenance of musculoskeletal homeostasis. Cartilage has been demonstrated to be highly mechanoresponsive, but the mechanisms by which chondrocytes respond to mechanical stimuli are not clearly understood. The goal of the study was to determine how LRP4, LRP5, and LRP6 within canonical Wnt-signaling are regulated in simulated microgravity and cyclic hydrostatic pressure, and to investigate the potential role of LRP 4/5/6 in cartilage degeneration. Rat chondrosacroma cell (RCS) pellets were stimulated using either cyclic hydrostatic pressure (1Hz, 7.5 MPa, 4hr/day) or simulated microgravity in a rotating wall vessel (RWV) bioreactor (11RPM, 24hr/day). LRP4/5/6 mRNA expression was assessed by RT-qPCR and LRP5 protein expression was determined by fluorescent immunostaining. To further evaluate our in vitro findings in vivo, mice were subjected to hindlimb suspension for 14 days and the femoral heads stained for LRP5 expression. We found that, in vitro, LRP4/5/6 mRNA expression is modulated in a time-dependent manner by mechanical stimulation. Additionally, LRP5 protein expression is upregulated in response to both simulated microgravity and cyclic hydrostatic pressure. LRP5 is also upregulated in vivo in the articular cartilage of hindlimb suspended mice. This is the first study to examine how LRP4/5/6, critical receptors within musculoskeletal biology, respond to mechanical stimulation. Further elucidation of this mechanism could provide significant clinical benefit for the identification of pharmaceutical targets for the maintenance of cartilage health.
first_indexed 2024-12-17T21:45:53Z
format Article
id doaj.art-95a80a9abaca43c6b5495740a3cba160
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-17T21:45:53Z
publishDate 2019-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-95a80a9abaca43c6b5495740a3cba1602022-12-21T21:31:28ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-011410e022324510.1371/journal.pone.0223245LRP receptors in chondrocytes are modulated by simulated microgravity and cyclic hydrostatic pressure.Rachel C NordbergLiliana F MellorAndrew R KrauseHenry J DonahueElizabeth G LoboaMechanical loading is essential for the maintenance of musculoskeletal homeostasis. Cartilage has been demonstrated to be highly mechanoresponsive, but the mechanisms by which chondrocytes respond to mechanical stimuli are not clearly understood. The goal of the study was to determine how LRP4, LRP5, and LRP6 within canonical Wnt-signaling are regulated in simulated microgravity and cyclic hydrostatic pressure, and to investigate the potential role of LRP 4/5/6 in cartilage degeneration. Rat chondrosacroma cell (RCS) pellets were stimulated using either cyclic hydrostatic pressure (1Hz, 7.5 MPa, 4hr/day) or simulated microgravity in a rotating wall vessel (RWV) bioreactor (11RPM, 24hr/day). LRP4/5/6 mRNA expression was assessed by RT-qPCR and LRP5 protein expression was determined by fluorescent immunostaining. To further evaluate our in vitro findings in vivo, mice were subjected to hindlimb suspension for 14 days and the femoral heads stained for LRP5 expression. We found that, in vitro, LRP4/5/6 mRNA expression is modulated in a time-dependent manner by mechanical stimulation. Additionally, LRP5 protein expression is upregulated in response to both simulated microgravity and cyclic hydrostatic pressure. LRP5 is also upregulated in vivo in the articular cartilage of hindlimb suspended mice. This is the first study to examine how LRP4/5/6, critical receptors within musculoskeletal biology, respond to mechanical stimulation. Further elucidation of this mechanism could provide significant clinical benefit for the identification of pharmaceutical targets for the maintenance of cartilage health.https://doi.org/10.1371/journal.pone.0223245
spellingShingle Rachel C Nordberg
Liliana F Mellor
Andrew R Krause
Henry J Donahue
Elizabeth G Loboa
LRP receptors in chondrocytes are modulated by simulated microgravity and cyclic hydrostatic pressure.
PLoS ONE
title LRP receptors in chondrocytes are modulated by simulated microgravity and cyclic hydrostatic pressure.
title_full LRP receptors in chondrocytes are modulated by simulated microgravity and cyclic hydrostatic pressure.
title_fullStr LRP receptors in chondrocytes are modulated by simulated microgravity and cyclic hydrostatic pressure.
title_full_unstemmed LRP receptors in chondrocytes are modulated by simulated microgravity and cyclic hydrostatic pressure.
title_short LRP receptors in chondrocytes are modulated by simulated microgravity and cyclic hydrostatic pressure.
title_sort lrp receptors in chondrocytes are modulated by simulated microgravity and cyclic hydrostatic pressure
url https://doi.org/10.1371/journal.pone.0223245
work_keys_str_mv AT rachelcnordberg lrpreceptorsinchondrocytesaremodulatedbysimulatedmicrogravityandcyclichydrostaticpressure
AT lilianafmellor lrpreceptorsinchondrocytesaremodulatedbysimulatedmicrogravityandcyclichydrostaticpressure
AT andrewrkrause lrpreceptorsinchondrocytesaremodulatedbysimulatedmicrogravityandcyclichydrostaticpressure
AT henryjdonahue lrpreceptorsinchondrocytesaremodulatedbysimulatedmicrogravityandcyclichydrostaticpressure
AT elizabethgloboa lrpreceptorsinchondrocytesaremodulatedbysimulatedmicrogravityandcyclichydrostaticpressure