Use of photosynthetic transgenic cyanobacteria to promote lymphangiogenesis in scaffolds for dermal regeneration
- PMID: 33753313
- DOI: 10.1016/j.actbio.2021.03.033
Use of photosynthetic transgenic cyanobacteria to promote lymphangiogenesis in scaffolds for dermal regeneration
Abstract
Impaired wound healing represents an unsolved medical need with a high impact on patients´ quality of life and global health care. Even though its causes are diverse, ischemic-hypoxic conditions and exacerbated inflammation are shared pathological features responsible for obstructing tissue restoration. In line with this, it has been suggested that promoting a normoxic pro-regenerative environment and accelerating inflammation resolution, by reinstating the lymphatic fluid transport, could allow the wound healing process to be resumed. Our group was first to demonstrate the functional use of scaffolds seeded with photosynthetic microorganisms to supply tissues with oxygen. Moreover, we previously proposed a photosynthetic gene therapy strategy to create scaffolds that deliver other therapeutic molecules, such as recombinant human growth factors into the wound area. In the present work, we introduce the use of transgenic Synechococcus sp. PCC 7002 cyanobacteria (SynHA), which can produce oxygen and lymphangiogenic hyaluronic acid, in photosynthetic biomaterials. We show that the co-culture of lymphatic endothelial cells with SynHA promotes their survival and proliferation under hypoxic conditions. Also, hyaluronic acid secreted by the cyanobacteria enhanced their lymphangiogenic potential as shown by changes to their gene expression profile, the presence of lymphangiogenic protein markers and their capacity to build lymph vessel tubes. Finally, by seeding SynHA into collagen-based dermal regeneration materials, we developed a viable photosynthetic scaffold that promotes lymphangiogenesis in vitro under hypoxic conditions. The results obtained in this study lay the groundwork for future tissue engineering applications using transgenic cyanobacteria that could become a therapeutic alternative for chronic wound treatment. STATEMENT OF SIGNIFICANCE: In this study, we introduce the use of transgenic Synechococcus sp. PCC 7002 (SynHA) cyanobacteria, which were genetically engineered to produce hyaluronic acid, to create lymphangiogenic photosynthetic scaffolds for dermal regeneration. Our results confirmed that SynHA cyanobacteria maintain their photosynthetic capacity under standard human cell culture conditions and efficiently proliferate when seeded inside fibrin-collagen scaffolds. Moreover, we show that SynHA supported the viability of co-cultured lymphatic endothelial cells (LECs) under hypoxic conditions by providing them with photosynthetic-derived oxygen, while cyanobacteria-derived hyaluronic acid stimulated the lymphangiogenic capacity of LECs. Since tissue hypoxia and impaired lymphatic drainage are two key factors that directly affect wound healing, our results suggest that lymphangiogenic photosynthetic biomaterials could become a treatment option for chronic wound management.
Keywords: Biomaterials; Hyaluronic acid; Hypoxia; Lymph vessels; Lymphatic endothelial cells; Oxygen; Synechococcus sp. PCC 7002.
Copyright © 2021. Published by Elsevier Ltd.
Conflict of interest statement
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Similar articles
-
Bioactivated scaffolds promote angiogenesis and lymphangiogenesis for dermal regeneration in vivo.J Tissue Eng. 2025 Mar 12;16:20417314251317542. doi: 10.1177/20417314251317542. eCollection 2025 Jan-Dec. J Tissue Eng. 2025. PMID: 40078220 Free PMC article.
-
Adipose-Derived Stem Cells Improve Angiogenesis and Lymphangiogenesis in a Hypoxic Dermal Regeneration Model In Vitro.Medicina (Kaunas). 2023 Apr 4;59(4):706. doi: 10.3390/medicina59040706. Medicina (Kaunas). 2023. PMID: 37109664 Free PMC article.
-
The use of commercial fibrin glue in dermal replacement material reduces angiogenic and lymphangiogenic gene and protein expression in vitro.J Biomater Appl. 2023 May;37(10):1858-1873. doi: 10.1177/08853282231171681. Epub 2023 Apr 21. J Biomater Appl. 2023. PMID: 37082911 Free PMC article.
-
Biomaterial Based Strategies for Engineering New Lymphatic Vasculature.Adv Healthc Mater. 2020 Sep;9(18):e2000895. doi: 10.1002/adhm.202000895. Epub 2020 Jul 30. Adv Healthc Mater. 2020. PMID: 32734721 Free PMC article. Review.
-
Modeling lymphangiogenesis: Pairing in vitro and in vivo metrics.Microcirculation. 2023 Apr;30(2-3):e12802. doi: 10.1111/micc.12802. Epub 2023 Feb 28. Microcirculation. 2023. PMID: 36760223 Free PMC article. Review.
Cited by
-
Hypoxic environment of wounds and photosynthesis-based oxygen therapy.Burns Trauma. 2024 Jun 10;12:tkae012. doi: 10.1093/burnst/tkae012. eCollection 2024. Burns Trauma. 2024. PMID: 38860010 Free PMC article. Review.
-
Current Status of Lymphangiogenesis: Molecular Mechanism, Immune Tolerance, and Application Prospect.Cancers (Basel). 2023 Feb 11;15(4):1169. doi: 10.3390/cancers15041169. Cancers (Basel). 2023. PMID: 36831512 Free PMC article. Review.
-
A First in Human Trial Implanting Microalgae Shows Safety of Photosynthetic Therapy for the Effective Treatment of Full Thickness Skin Wounds.Front Med (Lausanne). 2021 Nov 30;8:772324. doi: 10.3389/fmed.2021.772324. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34917636 Free PMC article.
-
Towards an In Vitro 3D Model for Photosynthetic Cancer Treatment: A Study of Microalgae and Tumor Cell Interactions.Int J Mol Sci. 2022 Nov 4;23(21):13550. doi: 10.3390/ijms232113550. Int J Mol Sci. 2022. PMID: 36362338 Free PMC article.
-
Dual roles of photosynthetic hydrogel with sustained oxygen generation in promoting cell survival and eradicating anaerobic infection.Mater Today Bio. 2024 Aug 10;28:101197. doi: 10.1016/j.mtbio.2024.101197. eCollection 2024 Oct. Mater Today Bio. 2024. PMID: 39221211 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials