Refrigerated amniotic membrane maintains its therapeutic qualities for 48 hours.

IF 4.3 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in Bioengineering and Biotechnology Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.3389/fbioe.2024.1455397
J Stelling-Férez, J M Puente-Cuadrado, V Álvarez-Yepes, S Alcaraz, E Tristante, I Hernández-Mármol, I Mompeán-Egea, A M García-Hernández, F J Nicolás
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引用次数: 0

Abstract

During wound healing, the migration of keratinocytes is critical for wound closure. The application of amniotic membrane (AM) on wounds with challenging contexts (e.g., chronification and diabetic foot ulcer) has proven very successful. However, the use of AM for clinical practice has several restraints when applied to patients; the most important restriction is preserving AM's therapeutic properties between its thawing and application onto the patient's wound. Moreover, AM collection and processing requires a cleanroom, together with specialized staff and equipment, and facilities that are not usually available in many hospitals and healthcare units. In this publication, we kept previously cryopreserved AM at different temperatures (37°C, 20°C, and 4°C) in different media (DMEM high glucose and saline solution with or without human albumin) and for long incubation time periods after thawing (24 h and 48 h). HaCaT keratinocytes and TGF-β1-chronified HaCaT keratinocytes were used to measure several parameters related to wound healing: migration, cell cycle arrest rescue, and the expression of key genes and migration-related proteins. Our findings indicate that AM kept in physiological saline solution at 4°C for 24 h or 48 h performed excellently in promoting HaCaT cell migration compared to AM that had been immediately thawed (0 h). Indeed, key proteins, extracellular signal-regulated kinase (ERK) and c-Jun, were induced by AM at 4°C in saline solution. Similarly, cell proliferation and different genes related to survival, inflammation, and senescence had, in all cases, the same response as to standard AM. These data suggest that the handling method in saline solution at 4°C does not interfere with AM's therapeutic properties.

冷藏羊膜的治疗效果可保持 48 小时。
在伤口愈合过程中,角质细胞的迁移对伤口闭合至关重要。事实证明,在具有挑战性的伤口(如慢性溃疡和糖尿病足溃疡)上应用羊膜非常成功。然而,将羊膜应用于临床实践有几个限制因素:最重要的限制因素是在羊膜解冻和应用于患者伤口之间要保持羊膜的治疗特性。此外,AM 的收集和处理需要洁净室、专业人员和设备,而许多医院和医疗单位通常都不具备这些设施。在这篇论文中,我们将先前冷冻保存的 AM 保存在不同温度(37°C、20°C 和 4°C)的不同培养基(DMEM 高糖和生理盐水,含或不含人血白蛋白)中,并在解冻后进行长时间培养(24 小时和 48 小时)。用 HaCaT 角质细胞和 TGF-β1 时序化的 HaCaT 角质细胞来测量与伤口愈合有关的几个参数:迁移、细胞周期停滞挽救、关键基因和迁移相关蛋白的表达。我们的研究结果表明,与立即解冻(0 小时)的 AM 相比,在 4°C 生理盐水溶液中保存 24 小时或 48 小时的 AM 在促进 HaCaT 细胞迁移方面表现出色。事实上,4°C生理盐水中的AM诱导了细胞外信号调节激酶(ERK)和c-Jun等关键蛋白。同样,细胞增殖和与存活、炎症和衰老有关的不同基因在所有情况下都对标准 AM 有相同的反应。这些数据表明,在 4°C 的生理盐水中处理 AM 的方法不会干扰 AM 的治疗特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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