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Subconjunctival Lymphatics Respond to VEGFC and Anti-Metabolites in Rabbit and Mouse Eyes

PURPOSE: To characterize and pharmacologically influence subconjunctival lymphatics in rabbit and mouse eyes. METHODS: Rabbits received subconjunctival injections of trypan blue or fixable fluorescent dextrans. Bleb-related outflow pathways were quantified. Immunofluorescence for vessel-specific mar...

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Detalles Bibliográficos
Autores principales: Lee, Jong Yeon, Wu, Jingyi, Liu, Yameng, Saraswathy, Sindhu, Zhou, Longfang, Bu, Qianwen, Su, Ying, Choi, Dongwon, Park, Eunkyung, Strohmaier, Clemens A., Weinreb, Robert N., Hong, Young-Kwon, Pan, Xiaojing, Huang, Alex S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526361/
https://www.ncbi.nlm.nih.gov/pubmed/36166215
http://dx.doi.org/10.1167/iovs.63.10.16
Descripción
Sumario:PURPOSE: To characterize and pharmacologically influence subconjunctival lymphatics in rabbit and mouse eyes. METHODS: Rabbits received subconjunctival injections of trypan blue or fixable fluorescent dextrans. Bleb-related outflow pathways were quantified. Immunofluorescence for vessel-specific markers (lymphatics [podoplanin and LYVE-1] and blood vessels [CD31]) were performed in native rabbit conjunctiva and after fixable fluorescent dextran injection. Vascular endothelial cell growth factor-C (VEGFC) was injected subconjunctivally in rabbits. mRNA and protein were assessed for the above markers using RT-PCR and Western blot. Alternatively, mouse studies used Prox1-tdTomato transgenic reporter mice. Subconjunctival injection conditions included: no injection, balanced salt solution (BSS), VEGFC, 5-fluorouracil (5FU) and two concentrations of mitomycin-C (MMC). Two mouse injection protocols (short and long) with different follow-up times and number of injections were performed. Mouse eyes were enucleated, flat mounts created, and subconjunctival branching and length assessed. RESULTS: Rabbit eyes demonstrated clear bleb-related subconjunctival outflow pathways that were distinct from blood vessels and were without nasal/temporal predilection. Immunofluorescence against vessel-specific markers showed lymphatics and blood vessels in rabbit conjunctiva, and these lymphatics overlapped with bleb-related subconjunctival outflow pathways. Subconjunctival VEGFC increased lymphatic (P = 0.004–0.04) but not blood vessel (P = 0.77–0.84) mRNA or protein in rabbits. Prox1-tdTomato transgenic reporter mice demonstrated natively fluorescent lymphatics. Subconjunctival VEGFC increased murine lymphatic branching and length (P ≤ 0.001–0.004) while antimetabolites (P ≤ 0.001–0.043) did the opposite for the long protocol. DISCUSSION: Subconjunctival lymphatics are pharmacologically responsive to both VEGFC and antimetabolites in two animal models studied using different methodologies. These results may be important for bleb-forming glaucoma surgeries or ocular drug delivery.