Page 417 - IJB-10-2
P. 417

International Journal of Bioprinting                            3D-bioprinted macrophage inflammation model




            therapeutic interventions, marking a significant stride   Conflict of interest
            toward personalized medicine.
                                                               The authors declare no conflicts of interest.
               The established model can be further expanded and
            modified, allowing for exploration of the multifaceted,   Author contributions
            dynamic processes of wound healing and regeneration,
            including tissue mimicry, macrophage behavior, and   Conceptualization: Nimal Raveendran, Kanchan Vaswani,
                                                                  Pingping Han, Corey S. Moran, Sašo Ivanovski
            intricate cell–cell  interactions. This  opens avenues  for   Formal analysis: Nimal Raveendran, Pingping Han, Corey
            a  more  comprehensive  understanding  of  physiological   S. Moran, Sašo Ivanovski
            processes and pathophysiological conditions, providing   Funding acquisition: Sašo Ivanovski
            a  robust foundation for  advancements in  regenerative   Investigation:  Nimal  Raveendran, Kanchan  Vaswani,
            medicine, drug development, and personalized healthcare.   Saraswat Basu
            The  versatility  of  the  developed  model  positions  it  as  a   Methodology: Nimal Raveendran, Kanchan Vaswani,
            valuable tool for unraveling the complexities of biological   Saraswat Basu, Sašo Ivanovski
            systems and holds promise for diverse applications in   Project administration: Nimal Raveendran, Corey S.
            biomedical research and clinical practice.
                                                                  Moran, Sašo Ivanovski
               In terms of future directions, a comprehensive study of   Supervision: Sašo Ivanovski
            all cells contributing to the inflammatory milieu would be   Validation: Nimal Raveendran, Pingping Han, Corey S. Moran
            important to model the entire inflammatory process. To   Visualization: Nimal Raveendran, Pingping Han
            this end, the current model requires further optimization   Writing – original draft: Nimal Raveendran, Kanchan Vaswani
            to accurately mimic the in vivo tissue inflammatory process   Writing – review & editing: Corey S. Moran, Sašo Ivanovski
            by characterization of a 3D construct carrying the myriad
            of different cells found in native tissues.        Ethics approval and consent to participate

            4. Conclusion                                      Not applicable.

            This study aimed to optimize the 3D bioprinting method   Consent for publication
            for THP-1 cells and evaluate macrophage differentiation   Not applicable.
            and polarization within the bioprinted construct under
            culture conditions. Optimal concentration of PMA and   Availability of data
            LPS for M0 differentiation and M1 polarization within
            the 3D-bioprinted model were determined, and the anti-  Data  is  available  from  the  corresponding  author  upon
            inflammatory action of Ibu against these cells within the   reasonable request.
            construct was demonstrated. However, further model
            validation is required using different pro-inflammatory   References
            stimuli and anti-inflammatory drugs. The 3D constructs
            developed in this study are limited in their ability to   1.   Merien F. A journey with Elie Metchnikoff: from innate
            replicate human tissues or organs due to the sole inclusion   cell mechanisms in infectious diseases to quantum biology.
                                                                  Front Public Health. 2016;4:125.
            of only a single cell type (macrophages). As such, this   doi: 10.3389/fpubh.2016.00125
            research serves as an important step toward establishing
            clinically relevant inflamed tissue models, and there is a   2.   Lokaj J, John C. Ilya Ilich Metchnikov and Paul Ehrlich:
            need for future studies to incorporate diverse cell types in   1908 Nobel Prize winners for their research on immunity.
                                                                  Epidemiol Mikrobiol Imunol. 2008;57(4):119-124.
            multicellular constructs to achieve more comprehensive
            replication of target tissues.                     3.   Wrzesinski K, Fey SJ. From 2D to 3D--a new dimension for
                                                                  modelling the effect of natural products on human tissue.
            Acknowledgments                                       Curr Pharm Des. 2015;21(38):5605-5616.
                                                                  doi: 10.2174/1381612821666151002114227
            The authors would like to thank Colgate-Palmolive, NY,   4.   Kapalczynska M, Kolenda T, Przybyla W, et al. 2D and 3D
            USA for their financial support.
                                                                  cell cultures - a comparison of different types of cancer cell
                                                                  cultures. Arch Med Sci. 2018;14(4):910-919.
            Funding                                               doi: 10.5114/aoms.2016.63743
            This research was funded by Colgate-Palmolive      5.   Jensen C, Teng Y. Is it time to start transitioning from 2D to
            industrial grant.                                     3D cell culture? Front Mol Biosci. 2020;7:33.


            Volume 10 Issue 2 (2024)                       409                                doi: 10.36922/ijb.2116
   412   413   414   415   416   417   418   419   420   421   422