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NELL-1 induces Sca-1+ mesenchymal progenitor cell expansion in models of bone maintenance and repair
Aaron W. James, … , Xinli Zhang, Chia Soo
Aaron W. James, … , Xinli Zhang, Chia Soo
Published June 15, 2017
Citation Information: JCI Insight. 2017;2(12):e92573. https://doi.org/10.1172/jci.insight.92573.
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Research Article Bone biology Cell biology

NELL-1 induces Sca-1+ mesenchymal progenitor cell expansion in models of bone maintenance and repair

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Abstract

NELL-1 is a secreted, osteogenic protein first discovered to control ossification of the cranial skeleton. Recently, NELL-1 has been implicated in bone maintenance. However, the cellular determinants of NELL-1’s bone-forming effects are still unknown. Here, recombinant human NELL-1 (rhNELL-1) implantation was examined in a clinically relevant nonhuman primate lumbar spinal fusion model. Prolonged rhNELL-1 protein release was achieved using an apatite-coated β-tricalcium phosphate carrier, resulting in a local influx of stem cell antigen-1–positive (Sca-1+) mesenchymal progenitor cells (MPCs), and complete osseous fusion across all samples (100% spinal fusion rate). Murine studies revealed that Nell-1 haploinsufficiency results in marked reductions in the numbers of Sca-1+CD45–CD31– bone marrow MPCs associated with low bone mass. Conversely, rhNELL-1 systemic administration in mice showed a marked anabolic effect accompanied by increased numbers of Sca-1+CD45–CD31– bone marrow MPCs. Mechanistically, rhNELL-1 induces Sca-1 transcription among MPCs, in a process requiring intact Wnt/β-catenin signaling. In summary, NELL-1 effectively induces bone formation across small and large animal models either via local implantation or intravenous delivery. NELL-1 induces an expansion of a bone marrow subset of MPCs with Sca-1 expression. These findings provide compelling justification for the clinical translation of a NELL-1–based therapy for local or systemic bone formation.

Authors

Aaron W. James, Jia Shen, Rebecca Tsuei, Alan Nguyen, Kevork Khadarian, Carolyn A. Meyers, Hsin Chuan Pan, Weiming Li, Jin H. Kwak, Greg Asatrian, Cymbeline T. Culiat, Min Lee, Kang Ting, Xinli Zhang, Chia Soo

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Figure 3

RhNELL-1 application in nonhuman primate lumbar spinal fusion: immunohistochemical analysis.

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RhNELL-1 application in nonhuman primate lumbar spinal fusion: immunohis...
(A) Immunofluorescent staining of nonhuman primate lumbar vertebral fusion segment from PBS, 1.0 mg/ml rhNELL-1, and 1.7 mg/ml rhNELL-1 treatment groups. From left to right: CD31/CD45+ cells appear green, stem cell antigen 1+ (Sca-1+) cells appear red, CD31/CD45+Sca-1+ cells appear yellow, and on the far right CD31–CD45–Sca-1+ cells appear red after digitally removing yellow fluorescence. Scale bars: 50 μm. (B) Quantification of CD31–CD45–Sca-1+ immunofluorescent staining in A. Six random images per sample were analyzed. n = 4 spinal fusion levels per treatment group, performed in single replicate. Data reported as mean ± SEM. **P < 0.01 compared with the PBS group. ##P < 0.01 compared with the 1.0 mg/ml rhNELL-1 group, using a 1-way ANOVA followed by a post-hoc Tukey’s test.

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