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破骨细胞驱动的聚多巴胺向多巴胺释放:用于聚多巴胺功能化组织工程支架的升级补丁

Osteoclast-Driven Polydopamine-to-Dopamine Release: An Upgrade Patch for Polydopamine-Functionalized Tissue Engineering Scaffolds.

作者信息

Wang Lufei, Hu Huamin, Ko Ching-Chang

机构信息

Guangxi Key Laboratory of Oral and Maxillofacial Rehabilitation and Reconstruction & College and Hospital of Stomatology, Guangxi Medical University, Nanning 530021, China.

Division of Oral and Craniofacial Health Sciences, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

J Funct Biomater. 2024 Jul 29;15(8):211. doi: 10.3390/jfb15080211.

Abstract

Polydopamine, a mussel-inspired self-adherent polymer of dopamine, has impressive adhesive properties and thus is one of the most versatile approaches to functionalize tissue engineering scaffolds. To date, many types of polydopamine-functionalized scaffolds have been manufactured and extensively applied in bone tissue engineering at the preclinical stage. However, how polydopamine is biodegraded and metabolized during the bone healing process and the side effects of its metabolite remain largely unknown. These issues are often neglected in the modern manufacture of polydopamine-functionalized materials and restrict them from stepping forward to clinical applications. In this study, using our bioinspired polydopamine-laced hydroxyapatite collagen calcium silicate material as a representative of polydopamine-functionalized tissue engineering scaffolds, we discovered that polydopamine can be metabolized to dopamine specifically by osteoclasts, which we termed "osteoclast-driven polydopamine-to-dopamine release". The released dopamine showed an osteoinductive effect in vitro and promoted bone regeneration in calvarial critical-sized defects. The concept of "osteoclast-driven polydopamine-to-dopamine release" has considerable application potential. It could be easily adopted by other existing polydopamine-functionalized scaffolds: just by recruiting osteoclasts. Once adopted, scaffolds will obtain a dopamine-releasing function, which enables their modulation of osteoblast activity and hence elevates the osteoinductive effect. Thus, "osteoclast-driven polydopamine-to-dopamine release" serves as an upgrade patch, which is useful for many existing polydopamine-functionalized materials.

摘要

聚多巴胺是一种受贻贝启发的多巴胺自粘附聚合物,具有令人印象深刻的粘附特性,因此是使组织工程支架功能化的最通用方法之一。迄今为止,许多类型的聚多巴胺功能化支架已被制造出来,并在临床前阶段广泛应用于骨组织工程。然而,聚多巴胺在骨愈合过程中如何被生物降解和代谢,以及其代谢产物的副作用在很大程度上仍然未知。在现代聚多巴胺功能化材料的制造中,这些问题常常被忽视,限制了它们向临床应用迈进。在本研究中,我们以受生物启发的聚多巴胺掺杂羟基磷灰石胶原硅酸钙材料作为聚多巴胺功能化组织工程支架的代表,发现聚多巴胺可被破骨细胞特异性代谢为多巴胺,我们将其称为“破骨细胞驱动的聚多巴胺向多巴胺释放”。释放的多巴胺在体外显示出骨诱导作用,并促进了颅骨临界尺寸缺损处的骨再生。“破骨细胞驱动的聚多巴胺向多巴胺释放”这一概念具有相当大的应用潜力。它可以很容易地被其他现有的聚多巴胺功能化支架采用:只需招募破骨细胞。一旦采用,支架将获得多巴胺释放功能,这使其能够调节成骨细胞活性,从而提高骨诱导作用。因此,“破骨细胞驱动的聚多巴胺向多巴胺释放”作为一个升级补丁,对许多现有的聚多巴胺功能化材料都很有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd2e/11355103/70d52202900e/jfb-15-00211-g001.jpg

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