Developing and characterising decellularized extracellular matrix hydrogels to bio-fabricate female reproductive tissues

This study investigated the development and characterization of decellularized extracellular matrix (dECM) hydrogels tailored for the bio-fabrication of female reproductive tissues, specifically targeting cortex, endometrium, medulla, and oviduct tissues. We aimed to evaluate the cytocompatibility, biomechanical properties, and overall efficacy of these dECMs in promoting cell viability, proliferation, and differentiation. Our findings revealed that these dECMs exhibited high biocompatibility with embryo development and cell viability, supporting micro vascularization and cellular differentiation without the need for external growth factors. These hydrogels displayed biomechanical properties that closely mimicked native tissues, which was vital for maintaining their functional integrity and supporting cellular activities. The printability assessments showed that dECMs, particularly those from cortex tissues, achieved high precision in replicating the intended structures, though challenges such as low porosity remained. The bioprinted constructs demonstrated robust cell growth, with over 97% viability observed by day 7, indicating their suitability for cell culture. This work represented a significant advancement in reproductive tissue bio-fabrication, demonstrating the potential of dECM-based hydrogels in creating structurally and functionally viable tissue constructs. By tailoring each dECM to match the unique biomechanical properties of different tissues, we paved the way for more effective and reliable applications in reproductive medicine and tissue engineering. HighlightsO_LIDeveloped decellularized extracellular matrix (dECM) bio-inks for bio-fabrication of female reproductive tissues. C_LIO_LIDemonstrated high biocompatibility with embryo development and cell viability. C_LIO_LIAchieved accurate bioprinting, maintaining structural integrity. C_LIO_LIPromoted micro vascularization and cell differentiation without added growth factors. C_LI