Refrigerated amniotic membrane maintains its therapeutic qualities for 48 hours

• Published in: Frontiers in bioengineering and biotechnology Vol. 12
• Main Authors: Stelling-Férez, J., Puente-Cuadrado, J. M., Álvarez-Yepes, V., Alcaraz, S., Tristante, E., Hernández-Mármol, I., Mompeán-Egea, I., García-Hernández, A. M., Nicolás, F. J.
• Format: Journal Article
• Language: English
• Published: Frontiers Media S.A 06.11.2024
• Subjects: amniotic membrane; cell migration; chronification; clinical application; conservation; keratinocytes
• ISSN: 2296-4185; 2296-4185
• DOI: 10.3389/fbioe.2024.1455397

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.