The study, led by Denis Jacob Machado, assistant professor at UNC Charlotte, and Vladimir Mashanov, staff scientist at Wake Forest, used RNA sequencing and advanced transmission electron microscopy to pinpoint 16 genes linked to tissue pliability. "We're uncovering the precise instructions that DNA sends to the cell," Jacob Machado explained, likening the process to decoding commands from a ship captain to its crew.
These discoveries, published in BMC Genomics under the title "Unveiling putative modulators of mutable collagenous tissue in the brittle star Ophiomastix wendtii: an RNA-Seq analysis," represent a significant step toward creating smart biomaterials capable of revolutionizing tissue regeneration and wound healing.
Through comparative tissue analyses, the team determined how gene expression within JLC-rich areas contributes to MCT modulation. Their work identified molecular mechanisms that could potentially be replicated in human biomedical applications, such as creating surgical glues or dynamic stents.
"This collagen matrix can change its pliability to become as soft or rigid as we want," Jacob Machado said, describing its potential to revolutionize biomedical tools. The next phase of research will explore how silencing certain genes affects MCT behavior, offering further insights into its regenerative potential.
"Our research puts science on an accelerated path to understanding cellular tissue regeneration," the researchers noted. Future work will focus on leveraging this understanding to engineer novel collagen-based biomaterials with tunable mechanical properties for tissue engineering and regenerative medicine.
This groundbreaking study underscores the possibilities for applying nature's design principles to advance human health.
Research Report:Unveiling putative modulators of mutable collagenous tissue in the brittle star Ophiomastix wendtii: an RNA-Seq analysis
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