Research Papers:
Cell properties of nucleus pulposus progenitor cells declines with intervertebral disc degeneration
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Xiao-Chuan Li1,2, Xue-Dong Bai1, Hong-Kui Xin1, Ying-Wei Bai1,3, Shi Cheng1, Tian-Yong Wen1, Shi-Sheng Pei1, Jing-Wei Ying1, De-Li Wang1, Qing He1 and Di-Ke Ruan1
1Department of Orthopaedic Surgery, Navy General Hospital, Beijing, 100048, China
2Department of Orthopaedic Surgery, Gaozhou People's Hospital, Guangdong, 525200, China
3Department of Orthopaedic Surgery, The Third People's Hospital of Huizhou, Guangdong, 516000, China
Correspondence to:
Di-Ke Ruan, email: [email protected]
Keywords: intervertebral disc, nucleus pulposus progenitor cells, cell properties, cell senescence, regenration medicine
Received: August 09, 2017 Accepted: September 20, 2017 Published: December 07, 2017
ABSTRACT
Endogenous repair of nucleus pulposus progenitor cells (NPPCs) has exhibited encouraging regenerative potential for treating intervertebral disc degeneration (IDD). However, few studies have explored the properties of NPPCs during the progression of IDD. Hence, additional studies are needed to characterize NPPCs from human degenerated intervertebral disc (IVDs) at different Pfirrmann grades. In this study, human NPPCs were isolated and identified from human IVDs with different Pfirrmann grades. Then, cell biological characteristics, including proliferation, colony formation, cell senescence, migration capacity and chondrogenic ability, were compared. NPPCs were successfully harvested from grade I to IV IVDs, but not from grade V IVD due to the marked loss of nucleus pulposus tissue at grade V, leading to poor cell cultures. All four grades of NPPCs were identified as mesenchymal stem cells (MSCs) based on the criteria of the International Society for Cellular Therapy (ISCT) and shared similar cell morphological characteristics. In addition decreasing trends in proliferation, colony-formation capacity, migration, and chondrogenic ability and increasing levels of cell senescence; were detected in cells from grade I to IV IVDs, with significant changes between NPPCs of grade II and III. In summary, compared with NPPCs from normal IVDs (grade I), cells from degenerated IVDs (grades II to IV) exhibited gradually decreased cell properties and increased cell senescence. Grade II NPPCs displayed the optimal regeneration potential, suggesting that these NPPCs are an ideal candidate for endogenous repair of IDD.