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The Nell-1 growth factor stimulates bone formation by purified human perivascular cells

Authors :
Chia Soo
Weiming Li
Zack Yin
Mirko Corselli
Hong Zhang
Zhong Zheng
Weiwei Chen
Pang Shen
Jia Shen
Min Lee
Janette N. Zara
Aaron W. James
Feng Chen
Jinny Kwak
Ben Wu
Bruno Péault
Xinli Zhang
Kang Ting
Ronald K. Siu
Source :
Zhang, X, Peault, B, Chen, W, Li, W, Corselli, M, James, A W, Lee, M, Siu, R K, Shen, P, Zheng, Z, Shen, J, Kwak, J, Zara, J N, Chen, F, Zhang, H, Yin, Z, Wu, B, Ting, K & Soo, C 2011, ' The Nell-1 Growth Factor Stimulates Bone Formation by Purified Human Perivascular Cells ', Tissue Engineering, Part A, vol. 17, no. 19-20, pp. 2497-2509 . https://doi.org/10.1089/ten.tea.2010.0705
Publication Year :
2011

Abstract

The search for novel sources of stem cells other than bone marrow mesenchymal stem cells (MSCs) for bone regeneration and repair has been a critical endeavor. We previously established an effective protocol to homogeneously purify human pericytes from multiple fetal and adult tissues, including adipose, bone marrow, skeletal muscle, and pancreas, and identified pericytes as a primitive origin of human MSCs. In the present study, we further characterized the osteogenic potential of purified human pericytes combined with a novel osteoinductive growth factor, Nell-1. Purified pericytes grown on either standard culture ware or human cancellous bone chip (hCBC) scaffolds exhibited robust osteogenic differentiation in vitro. Using a nude mouse muscle pouch model, pericytes formed significant new bone in vivo as compared to scaffold alone (hCBC). Moreover, Nell-1 significantly increased pericyte osteogenic differentiation, both in vitro and in vivo. Interestingly, Nell-1 significantly induced pericyte proliferation and was observed to have pro-angiogenic effects, both in vitro and in vivo. These studies suggest that pericytes are a potential new cell source for future efforts in skeletal regenerative medicine, and that Nell-1 is a candidate growth factor able to induce pericyte osteogenic differentiation.

Details

ISSN :
1937335X
Volume :
17
Issue :
19-20
Database :
OpenAIRE
Journal :
Tissue engineering. Part A
Accession number :
edsair.doi.dedup.....3a1ebdfb042855c1ba7f5d12e20d7bd2