The response of nucleus pulposus cell senescence to static and dynamic compressions in a disc organ culture.

Author: Shi J1, Pang L2, Jiao S3
Affiliation:
1Liaocheng People's Hospital and Liaocheng Clinical School of Taishan Medical University, Liaocheng, China.
2Department of Spine Surgery, Liaocheng People's Hospital, Liaocheng, 252000, Shandong, China, Liaocheng, China.
3Department of Orthopaedics, Yantai Yeda Hospital, Yantai, 264006, Shandong, China, Liaocheng, China shouguojiao0113@sina.com.
Conference/Journal: Biosci Rep.
Date published: 2018 Feb 5
Other: Pages: BSR20180064 , Special Notes: doi: 10.1042/BSR20180064. [Epub ahead of print] , Word Count: 185


BACKGROUND: Mechanical stimuli obviously affect disc nucleus pulposus (NP) biology. Previous studies have indicate that static compression exhibits detrimental effects on disc biology compared with dynamic compression.

OBJECTIVE: To study disc NP cell senescence under static compression and dynamic compression in a disc organ culture.

METHODS: Porcine discs were cultured and subjected to compression (static compression: 0.4 MPa for 4 hours once per day; dynamic compression: 0.4 MPa at a frequency of 1.0 Hz for 4 hours once per day) for 7 days using a self-developed mechanically active bioreactor. The non-compressed discs were used as controls.

RESULTS: Compared with the dynamic compression, static compression significantly promoted disc NP cell senescence, reflected by the increased senescence associated β-galactosidase (SA-β-Gal) activity, senescence-associated heterochromatic foci (SAHF) formation and senescence markers expression, and the decreased telomerase activity and NP matrix biosynthesis.

CONCLUSION: Static compression accelerates disc NP cell senescence compared with the dynamic compression in a disc organ culture. This study provides that acceleration of NP cell senescence may be involved in previously reported static compression-mediated disc NP degenerative changes.

©2018 The Author(s).

KEYWORDS: compression; degeneration; nucleus pulposus; organ culture; senescence

PMID: 29437905 DOI: 10.1042/BSR20180064

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