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免疫和炎症途径参与固有骨髓骨化。

Immune and inflammatory pathways are involved in inherent bone marrow ossification.

机构信息

Harvard-MIT Division of Health Sciences and Technology, Brigham and Women's Hospital, Harvard Medical School, 65 Landsdowne Street, PRB 252, Cambridge, MA 02139, USA.

出版信息

Clin Orthop Relat Res. 2012 Sep;470(9):2528-40. doi: 10.1007/s11999-012-2459-4.

Abstract

BACKGROUND

Bone marrow plays a key role in bone formation and healing. Although a subset of marrow explants ossifies in vitro without excipient osteoinductive factors, some explants do not undergo ossification. The disparity of outcome suggests a significant heterogeneity in marrow tissue in terms of its capacity to undergo osteogenesis.

QUESTIONS/PURPOSES: We sought to identify: (1) proteins and signaling pathways associated with osteogenesis by contrasting the proteomes of ossified and poorly ossified marrow explants; and (2) temporal changes in proteome and signaling pathways of marrow ossification in the early and late phases of bone formation.

METHODS

Explants of marrow were cultured. Media conditioned by ossified (n = 4) and poorly ossified (n = 4) subsets were collected and proteins unique to each group were identified by proteomic analysis. Proteomic data were processed to assess proteins specific to the early phase (Days 1-14) and late phase (Days 15-28) of the culture period. Pathways involved in bone marrow ossification were identified through bioinformatics.

RESULTS

Twenty-eight proteins were unique to ossified samples and eight were unique to poorly ossified ones. Twelve proteins were expressed during the early phase and 15 proteins were specific to the late phase. Several identified pathways corroborated those reported for bone formation in the literature. Immune and inflammatory pathways were specific to ossified samples.

CONCLUSIONS

The marrow explant model indicates the inflammatory and immune pathways to be an integral part of the osteogenesis process.

摘要

背景

骨髓在骨骼形成和修复中起着关键作用。尽管一部分骨髓外植体在没有赋形剂成骨诱导因子的情况下在体外发生骨化,但仍有一些外植体不发生骨化。结果的差异表明骨髓组织在成骨能力方面存在显著的异质性。

问题/目的:我们试图通过对比骨化和骨化不良的骨髓外植体的蛋白质组,来确定:(1)与成骨相关的蛋白质和信号通路;(2)在骨形成的早期和晚期阶段,骨髓骨化的蛋白质组和信号通路的时间变化。

方法

培养骨髓外植体。收集骨化(n = 4)和骨化不良(n = 4)亚组的条件培养基,并通过蛋白质组学分析鉴定每个组特有的蛋白质。对蛋白质组数据进行处理,以评估培养期早期(第 1-14 天)和晚期(第 15-28 天)的特定蛋白质。通过生物信息学鉴定涉及骨髓骨化的途径。

结果

28 种蛋白质是骨化样本特有的,8 种蛋白质是骨化不良样本特有的。有 12 种蛋白质在早期表达,15 种蛋白质是晚期特有的。一些确定的途径与文献中报道的骨形成途径相吻合。免疫和炎症途径是骨化样本所特有的。

结论

骨髓外植体模型表明,炎症和免疫途径是成骨过程的一个组成部分。

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本文引用的文献

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A 3D in vitro bone organ model using human progenitor cells.使用人源祖细胞的 3D 体外骨器官模型。
Eur Cell Mater. 2011 May 15;21:445-58; discussion 458. doi: 10.22203/ecm.v021a33.
2
A scaffold-free multicellular three-dimensional in vitro model of osteogenesis.无支架的多细胞三维体外成骨模型。
Calcif Tissue Int. 2011 May;88(5):388-401. doi: 10.1007/s00223-011-9467-3. Epub 2011 Feb 12.
4
Co-culture systems for vascularization--learning from nature.用于血管生成的共培养系统——向大自然学习。
Adv Drug Deliv Rev. 2011 Apr 30;63(4-5):291-9. doi: 10.1016/j.addr.2011.01.009. Epub 2011 Jan 31.

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