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新型类人胶原蛋白,最大限度促进 BMP-2 敏感释放,显著修复骨缺损。

Newly Designed Human-Like Collagen to Maximize Sensitive Release of BMP-2 for Remarkable Repairing of Bone Defects.

机构信息

Provincial Key Laboratory of Biotechnology of Shaanxi, Northwest University, 229 TaiBai North Road, Xi'an 710069, Shaanxi, China.

Key Laboratory of Resource Biology and Modern Biotechnology in Western China, Ministry of Education, Northwest University, 229 TaiBai North Road, Xi'an 710069, Shaanxi, China.

出版信息

Biomolecules. 2019 Sep 4;9(9):450. doi: 10.3390/biom9090450.

DOI:10.3390/biom9090450
PMID:31487971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6769454/
Abstract

Designing the "ideal" hydrogel/matrix which can load bone morphogenetic protein-2 (BMP-2) in a low dose and with a sustained release is the key for its successful therapeutic application to enhance osteogenesis. The current use of natural collagen sponges as hydrogel/matrix is limited due to the collagen matrix showing weak mechanical strength and unmanageable biodegradability. Furthermore, the efficiency and safe dose usage of the BMP-2 has never been seriously considered other than purely chasing the lowest dose usage and extended-release time. In this paper, we customized a novel enzymatically cross-linked recombinant human-like collagen (HLC) sponge with low immunogenicity, little risk from hidden viruses, and easy production. We obtained a unique vertical pore structure and the porosity of the HLC, which are beneficial for Mesenchymal stem cells (MSCs) migration into the HLC sponge and angiopoiesis. This HLC sponge loading with low dose BMP-2 (1 µg) possessed high mechanical strength along with a burst and a sustained release profile. These merits overcome previous limitations of HLC in bone repair and are safer and more sensitive than commercial collagens. For the first time, we identified that a 5 µg dose of BMP-2 can bring about the side effect of bone overgrowth through this sensitive delivery system. Osteoinduction of the HLC-BMP sponges was proved by an in vivo mouse ectopic bone model and a rat cranial defect repair model. The method and the HLC-BMP sponge have the potential to release other growth factors and aid other tissue regeneration. Additionally, the ability to mass-produce HLC in our study overcomes the current supply shortage, which limits bone repair in the clinic.

摘要

设计“理想的”水凝胶/基质,使其能够以低剂量和持续释放负载骨形态发生蛋白-2(BMP-2),是其成功治疗应用以增强成骨作用的关键。由于胶原基质表现出较弱的机械强度和难以控制的生物降解性,当前将天然胶原海绵用作水凝胶/基质的用途受到限制。此外,除了纯粹追求最低剂量使用和延长释放时间之外,BMP-2 的效率和安全剂量使用从未得到认真考虑。在本文中,我们定制了一种新型的酶交联重组人样胶原(HLC)海绵,具有低免疫原性、低隐藏病毒风险和易于生产的特点。我们获得了独特的垂直孔结构和 HLC 的孔隙率,有利于间充质干细胞(MSCs)迁移到 HLC 海绵和血管生成。这种装载低剂量 BMP-2(1µg)的 HLC 海绵具有较高的机械强度,同时具有爆发性和持续释放特性。这些优点克服了 HLC 在骨修复中的先前限制,并且比商业胶原更安全、更敏感。我们首次通过这种敏感的递送系统确定 5µg 剂量的 BMP-2 会引起骨过度生长的副作用。通过体内小鼠异位骨模型和大鼠颅缺损修复模型证明了 HLC-BMP 海绵的成骨诱导作用。该方法和 HLC-BMP 海绵具有释放其他生长因子和辅助其他组织再生的潜力。此外,我们在研究中大规模生产 HLC 的能力克服了目前限制临床骨修复的供应短缺问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/1748bdbf8935/biomolecules-09-00450-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/ac628e0689c4/biomolecules-09-00450-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/824d61ba32c3/biomolecules-09-00450-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/90e675ce17fb/biomolecules-09-00450-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/7c4f27ae6c15/biomolecules-09-00450-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/d6e7af7de928/biomolecules-09-00450-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/deda73dcf934/biomolecules-09-00450-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/1748bdbf8935/biomolecules-09-00450-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/ac628e0689c4/biomolecules-09-00450-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/8be132188671/biomolecules-09-00450-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/824d61ba32c3/biomolecules-09-00450-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/90e675ce17fb/biomolecules-09-00450-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/7c4f27ae6c15/biomolecules-09-00450-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/d6e7af7de928/biomolecules-09-00450-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/deda73dcf934/biomolecules-09-00450-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5093/6769454/1748bdbf8935/biomolecules-09-00450-g008.jpg

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