Decellularized kidney extracellular matrix-based hydrogels for renal tissue engineering

IF 9.4 1区 医学 Q1 ENGINEERING, BIOMEDICAL Acta Biomaterialia Pub Date : 2024-05-01 DOI:10.1016/j.actbio.2024.04.026
Rita Quinteira , Sara Gimondi , Nelson O. Monteiro , Rita Sobreiro-Almeida , Laura Lasagni , Paola Romagnani , Nuno M. Neves
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Abstract

Kidney regeneration is hindered by the limited pool of intrinsic reparative cells. Advanced therapies targeting renal regeneration have the potential to alleviate the clinical and financial burdens associated with kidney disease. Delivery systems for cells, extracellular vesicles, or growth factors aimed at enhancing regeneration can benefit from vehicles enabling targeted delivery and controlled release. Hydrogels, optimized to carry biological cargo while promoting regeneration, have emerged as promising candidates for this purpose. This study aims to develop a hydrogel from decellularized kidney extracellular matrix (DKECM) and explore its biocompatibility as a biomaterial for renal regeneration. The resulting hydrogel crosslinks with temperature and exhibits a high concentration of extracellular matrix. The decellularization process efficiently removes detergent residues, yielding a pathogen-free biomaterial that is non-hemolytic and devoid of α-gal epitope. Upon interaction with macrophages, the hydrogel induces differentiation into both pro-inflammatory and anti-inflammatory phenotypes, suggesting an adequate balance to promote biomaterial functionality in vivo. Renal progenitor cells encapsulated in the DKECM hydrogel demonstrate higher viability and proliferation than in commercial collagen-I hydrogels, while also expressing tubular cells and podocyte markers in long-term culture.

Overall, the injectable biomaterial derived from porcine DKECM is anticipated to elicit minimal host reaction while fostering progenitor cell bioactivity, offering a potential avenue for enhancing renal regeneration in clinical settings.

Statement of significance

The quest to improve treatments for kidney disease is crucial, given the challenges faced by patients on dialysis or waiting for transplants. Exciting new therapies combining biomaterials with cells can revolutionize kidney repair. In this study, researchers created a hydrogel from pig kidney. This gel could be used to deliver cells and other substances that help in kidney regeneration. Despite coming from pigs, it's safe for use in humans, with no harmful substances and reduced risk of immune reactions. Importantly, it promotes a balanced healing response in the body. This research not only advances our knowledge of kidney repair but also offers hope for more effective treatments for kidney diseases.

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用于肾组织工程的脱细胞肾脏细胞外基质水凝胶
肾脏再生受到内在修复细胞库有限的阻碍。针对肾脏再生的先进疗法有可能减轻与肾脏疾病相关的临床和经济负担。旨在促进再生的细胞、细胞外囊泡或生长因子输送系统可受益于定向输送和控制释放的载体。水凝胶经过优化,既能携带生物货物,又能促进再生,已成为实现这一目的的理想候选材料。本研究旨在利用脱细胞肾脏细胞外基质(DKECM)开发一种水凝胶,并探索其作为肾脏再生生物材料的生物相容性。这种水凝胶会随温度升高而交联,并显示出高浓度的细胞外基质。脱细胞过程可有效去除洗涤剂残留物,从而获得不溶血、无α-gal表位的无病原体生物材料。在与巨噬细胞相互作用时,水凝胶会诱导巨噬细胞分化成促炎和抗炎两种表型,这表明水凝胶在促进生物材料在体内发挥功能方面达到了适当的平衡。包裹在 DKECM 水凝胶中的肾祖细胞比包裹在商用胶原蛋白-I 水凝胶中的肾祖细胞具有更高的存活率和增殖能力,同时在长期培养中还能表达肾小管细胞和荚膜细胞标记。总之,从猪 DKECM 中提取的可注射生物材料预计会引起最小的宿主反应,同时促进祖细胞的生物活性,为在临床环境中加强肾脏再生提供了潜在的途径。令人兴奋的新疗法将生物材料与细胞结合在一起,可以彻底改变肾脏修复的方式。在这项研究中,研究人员从猪肾中提取了一种水凝胶。这种凝胶可用于输送有助于肾脏再生的细胞和其他物质。尽管这种凝胶来自猪肾,但它对人体是安全的,不含任何有害物质,而且降低了免疫反应的风险。重要的是,它能促进体内平衡的愈合反应。这项研究不仅增进了我们对肾脏修复的了解,也为更有效地治疗肾脏疾病带来了希望。
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来源期刊
Acta Biomaterialia
Acta Biomaterialia 工程技术-材料科学:生物材料
CiteScore
16.80
自引率
3.10%
发文量
776
审稿时长
30 days
期刊介绍: Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.
期刊最新文献
Editorial Board Editorial Board Erratum to “Anti-fibrotic and anti-stricture effects of biodegradable biliary stents braided with dexamethasone-impregnated sheath/core structured monofilaments” [Acta Biomaterialia. Volume 178, 1 April 2024, Pages 137-146] Corrigendum to “Optimizing the cell compatibility and mechanical properties in TiZrNbTa medium-entropy alloy/β-Ti composites through phase transformation” [Acta Biomaterialia. Volume 181, June 2024, Pages 469-482] Association between neural stem/progenitor cells and biomaterials in spinal cord injury therapies: A systematic review and network meta-analysis
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