The Reparative Ability of the Aligned Decellularized Annulus Fibrosus Matrix/Poly(Ether Carbonate Urethane)Urea Blended Fibrous Scaffolds on Annulus Fibrosus Defects
{"title":"The Reparative Ability of the Aligned Decellularized Annulus Fibrosus Matrix/Poly(Ether Carbonate Urethane)Urea Blended Fibrous Scaffolds on Annulus Fibrosus Defects","authors":"Yifeng Li, Yu Zhang, Chen Liu","doi":"10.1002/jbm.a.70140","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Currently, there is a lack of effective methods to repair annulus fibrosus (AF) defects in clinical practice. Therefore, exploring strategies to promote AF regeneration is of significant importance for delaying intervertebral disc degeneration. In recent years, tissue engineering technology has become a hotspot in the field of AF repair, offering promising treatments for intervertebral disc degenerative diseases. Studies have shown that surface structural characteristics, such as the fiber orientation of scaffold materials, play a crucial role in regulating the differentiation of cells adhering to the scaffold surface. Here we used electrospinning technology to prepare aligned and random decellularized annulus fibrosus matrix (DAFM)/poly(ether carbonate urethane)urea (PECUU) blended fibrous scaffolds. Rat AF stem cells (AFSCs) cultured on the aligned DAFM/PECUU blended fibrous scaffolds exhibited an aligned distribution, and the secreted AF-associated extracellular matrix components, including <i>Collagen type I</i>, <i>Collagen type II</i>, and <i>Aggrecan</i>, were also aligned. In contrast, AFSCs on the random DAFM/PECUU blended fibrous scaffolds exhibited an irregular distribution, and the secreted AF-associated extracellular matrix components were also irregularly distributed. Moreover, AFSCs on the aligned DAFM/PECUU blended fibrous scaffolds expressed higher levels of <i>Col-I</i> and <i>Aggrecan</i> than those on the random DAFM/PECUU blended fibrous scaffold. Both aligned and random DAFM/PECUU blended fibrous scaffolds degraded slowly in vivo. Magnetic resonance imaging, hematoxylin and eosin staining, Safranin O-fast green staining, and immunohistochemical staining demonstrated that both aligned and random DAFM/PECUU blended fibrous scaffolds effectively repaired AF defects in rats in vivo. However, the aligned DAFM/PECUU blended fibrous scaffolds exhibited superior repair capability.</p>\n </div>","PeriodicalId":15142,"journal":{"name":"Journal of biomedical materials research. Part A","volume":"114 8","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2026-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biomedical materials research. Part A","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jbm.a.70140","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Currently, there is a lack of effective methods to repair annulus fibrosus (AF) defects in clinical practice. Therefore, exploring strategies to promote AF regeneration is of significant importance for delaying intervertebral disc degeneration. In recent years, tissue engineering technology has become a hotspot in the field of AF repair, offering promising treatments for intervertebral disc degenerative diseases. Studies have shown that surface structural characteristics, such as the fiber orientation of scaffold materials, play a crucial role in regulating the differentiation of cells adhering to the scaffold surface. Here we used electrospinning technology to prepare aligned and random decellularized annulus fibrosus matrix (DAFM)/poly(ether carbonate urethane)urea (PECUU) blended fibrous scaffolds. Rat AF stem cells (AFSCs) cultured on the aligned DAFM/PECUU blended fibrous scaffolds exhibited an aligned distribution, and the secreted AF-associated extracellular matrix components, including Collagen type I, Collagen type II, and Aggrecan, were also aligned. In contrast, AFSCs on the random DAFM/PECUU blended fibrous scaffolds exhibited an irregular distribution, and the secreted AF-associated extracellular matrix components were also irregularly distributed. Moreover, AFSCs on the aligned DAFM/PECUU blended fibrous scaffolds expressed higher levels of Col-I and Aggrecan than those on the random DAFM/PECUU blended fibrous scaffold. Both aligned and random DAFM/PECUU blended fibrous scaffolds degraded slowly in vivo. Magnetic resonance imaging, hematoxylin and eosin staining, Safranin O-fast green staining, and immunohistochemical staining demonstrated that both aligned and random DAFM/PECUU blended fibrous scaffolds effectively repaired AF defects in rats in vivo. However, the aligned DAFM/PECUU blended fibrous scaffolds exhibited superior repair capability.
期刊介绍:
The Journal of Biomedical Materials Research Part A is an international, interdisciplinary, English-language publication of original contributions concerning studies of the preparation, performance, and evaluation of biomaterials; the chemical, physical, toxicological, and mechanical behavior of materials in physiological environments; and the response of blood and tissues to biomaterials. The Journal publishes peer-reviewed articles on all relevant biomaterial topics including the science and technology of alloys,polymers, ceramics, and reprocessed animal and human tissues in surgery,dentistry, artificial organs, and other medical devices. The Journal also publishes articles in interdisciplinary areas such as tissue engineering and controlled release technology where biomaterials play a significant role in the performance of the medical device.
The Journal of Biomedical Materials Research is the official journal of the Society for Biomaterials (USA), the Japanese Society for Biomaterials, the Australasian Society for Biomaterials, and the Korean Society for Biomaterials.
Articles are welcomed from all scientists. Membership in the Society for Biomaterials is not a prerequisite for submission.