Calcium‐dependent deceleration of the cell cycle in muscle cells by simulated microgravity. Issue 5 (30th January 2013)
- Record Type:
- Journal Article
- Title:
- Calcium‐dependent deceleration of the cell cycle in muscle cells by simulated microgravity. Issue 5 (30th January 2013)
- Main Title:
- Calcium‐dependent deceleration of the cell cycle in muscle cells by simulated microgravity
- Authors:
- Damm, Tatiana Benavides
Richard, Stéphane
Tanner, Samuel
Wyss, Fabienne
Egli, Marcel
Franco‐Obregón, Alfredo - Abstract:
- Abstract : Of all our mechanosensitive tissues, skeletal muscle is the most developmentally responsive to physical activity. Conversely, restricted mobility due to injury or disease results in muscle atrophy. Gravitational force is another form of mechanical input with profound developmental consequences. The mechanical unloading resulting from the reduced gravitational force experienced during spaceflight results in oxidative muscle loss. We examined the early stages of myogenesis under conditions of simulated microgravity (SM). C2C12 mouse myoblasts in SM proliferated more slowly (2.23× less) as a result of their being retained longer within the G2 /M phase of the cell cycle (2.10× more) relative to control myoblasts at terrestrial gravity. Blocking calcium entry via TRP channels with SKF‐96365 (10–20 μM) accumulated myoblasts within the G2 /M phase of the cell cycle and retarded their proliferation. On the genetic level, SM resulted in the reduced expression of TRPC1 and IGF‐1 isoforms, transcriptional events regulated by calcium downstream of mechanical input. A decrease in TRPC1‐mediated calcium entry thus appears to be a pivotal event in the muscle atrophy brought on by gravitational mechanical unloading. Hence, relieving the constant force of gravity on cells might prove one valid experimental approach to expose the underlying mechanisms modulating mechanically regulated developmental programs.—Benavides Damm, T., Richard, S., Tanner, S., Wyss, F., Egli, M.,Abstract : Of all our mechanosensitive tissues, skeletal muscle is the most developmentally responsive to physical activity. Conversely, restricted mobility due to injury or disease results in muscle atrophy. Gravitational force is another form of mechanical input with profound developmental consequences. The mechanical unloading resulting from the reduced gravitational force experienced during spaceflight results in oxidative muscle loss. We examined the early stages of myogenesis under conditions of simulated microgravity (SM). C2C12 mouse myoblasts in SM proliferated more slowly (2.23× less) as a result of their being retained longer within the G2 /M phase of the cell cycle (2.10× more) relative to control myoblasts at terrestrial gravity. Blocking calcium entry via TRP channels with SKF‐96365 (10–20 μM) accumulated myoblasts within the G2 /M phase of the cell cycle and retarded their proliferation. On the genetic level, SM resulted in the reduced expression of TRPC1 and IGF‐1 isoforms, transcriptional events regulated by calcium downstream of mechanical input. A decrease in TRPC1‐mediated calcium entry thus appears to be a pivotal event in the muscle atrophy brought on by gravitational mechanical unloading. Hence, relieving the constant force of gravity on cells might prove one valid experimental approach to expose the underlying mechanisms modulating mechanically regulated developmental programs.—Benavides Damm, T., Richard, S., Tanner, S., Wyss, F., Egli, M., Franco‐Obregón, A. Calcium‐dependent deceleration of the cell cycle in muscle cells by simulated microgravity. FASEB J. 27, 2045–2054 (2013). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 27:Issue 5(2013)
- Journal:
- FASEB journal
- Issue:
- Volume 27:Issue 5(2013)
- Issue Display:
- Volume 27, Issue 5 (2013)
- Year:
- 2013
- Volume:
- 27
- Issue:
- 5
- Issue Sort Value:
- 2013-0027-0005-0000
- Page Start:
- 2045
- Page End:
- 2054
- Publication Date:
- 2013-01-30
- Subjects:
- mechanotransduction -- transient receptor potential canonical type 1 -- TRPC1 -- insulin‐like growth factor 1 -- IGF‐1
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.12-218693 ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13220.xml