Cargando…
An Engineered Human Fibroblast Growth Factor-1 Derivative, TTHX1114, Ameliorates Short-term Corneal Nitrogen Mustard Injury in Rabbit Organ Cultures
PURPOSE: Organ cultures of rabbit corneas have been used to ascertain the effectiveness of a human fibroblast growth factor (FGF)-1 derivative (TTHX1114), lacking cysteine residues, to protect against and/or repair epithelial lesions following exposure to nitrogen mustard (NM). METHODS: Rabbit corne...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155473/ https://www.ncbi.nlm.nih.gov/pubmed/30267094 http://dx.doi.org/10.1167/iovs.18-24568 |
_version_ | 1783357907707887616 |
---|---|
author | Eveleth, David D. Eveleth, Jennifer J. Subramaniam, Amuthakannan Hahn, Rita Zhou, Peihong Gordon, Marion K. Bradshaw, Ralph A. |
author_facet | Eveleth, David D. Eveleth, Jennifer J. Subramaniam, Amuthakannan Hahn, Rita Zhou, Peihong Gordon, Marion K. Bradshaw, Ralph A. |
author_sort | Eveleth, David D. |
collection | PubMed |
description | PURPOSE: Organ cultures of rabbit corneas have been used to ascertain the effectiveness of a human fibroblast growth factor (FGF)-1 derivative (TTHX1114), lacking cysteine residues, to protect against and/or repair epithelial lesions following exposure to nitrogen mustard (NM). METHODS: Rabbit corneas were exposed to NM and cultured for up to 14 days, with or without drug (TTHX1114). At specified times, tissue was examined by histopathology and graded by a novel composite scale. Proliferation was measured by 5-ethynyl-2′-deoxyuridine (EdU) incorporation, and the expression of native FGF-1 and ADAM-17 after NM exposure was determined by immunofluorescence. RESULTS: Rabbit corneas, exposed to a single dose of NM, showed a nearly complete loss of epithelial cells by day 6 but were significantly regenerated by day 14. When treated continuously with TTHX1114 following vesicant exposure, the losses remained at day 2 levels. The loss of keratocytes in the stroma was not affected by TTHX1114. EdU incorporation over the same time course showed a steady increase in tissue that had not been treated with TTHX1114, while corneas that were treated with the drug showed a higher percent incorporation initially, which then decreased, indicating the strong proliferative response to TTHX1114. ADAM-17 was not significantly altered by TTHX1114 treatment. Corneal epithelial FGF-1 disappeared after only 1 day following exposure to NM. CONCLUSIONS: TTHX1114 is protective against NM-induced damage of the corneal epithelium, possibly by supplying an NM-resistant source of trophic support and by stimulating regeneration of new epithelial cells. These responses underscore the potential value of TTHX1114 as an anti-vesicant therapeutic. |
format | Online Article Text |
id | pubmed-6155473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-61554732018-09-26 An Engineered Human Fibroblast Growth Factor-1 Derivative, TTHX1114, Ameliorates Short-term Corneal Nitrogen Mustard Injury in Rabbit Organ Cultures Eveleth, David D. Eveleth, Jennifer J. Subramaniam, Amuthakannan Hahn, Rita Zhou, Peihong Gordon, Marion K. Bradshaw, Ralph A. Invest Ophthalmol Vis Sci Cornea PURPOSE: Organ cultures of rabbit corneas have been used to ascertain the effectiveness of a human fibroblast growth factor (FGF)-1 derivative (TTHX1114), lacking cysteine residues, to protect against and/or repair epithelial lesions following exposure to nitrogen mustard (NM). METHODS: Rabbit corneas were exposed to NM and cultured for up to 14 days, with or without drug (TTHX1114). At specified times, tissue was examined by histopathology and graded by a novel composite scale. Proliferation was measured by 5-ethynyl-2′-deoxyuridine (EdU) incorporation, and the expression of native FGF-1 and ADAM-17 after NM exposure was determined by immunofluorescence. RESULTS: Rabbit corneas, exposed to a single dose of NM, showed a nearly complete loss of epithelial cells by day 6 but were significantly regenerated by day 14. When treated continuously with TTHX1114 following vesicant exposure, the losses remained at day 2 levels. The loss of keratocytes in the stroma was not affected by TTHX1114. EdU incorporation over the same time course showed a steady increase in tissue that had not been treated with TTHX1114, while corneas that were treated with the drug showed a higher percent incorporation initially, which then decreased, indicating the strong proliferative response to TTHX1114. ADAM-17 was not significantly altered by TTHX1114 treatment. Corneal epithelial FGF-1 disappeared after only 1 day following exposure to NM. CONCLUSIONS: TTHX1114 is protective against NM-induced damage of the corneal epithelium, possibly by supplying an NM-resistant source of trophic support and by stimulating regeneration of new epithelial cells. These responses underscore the potential value of TTHX1114 as an anti-vesicant therapeutic. The Association for Research in Vision and Ophthalmology 2018-09 /pmc/articles/PMC6155473/ /pubmed/30267094 http://dx.doi.org/10.1167/iovs.18-24568 Text en Copyright 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Cornea Eveleth, David D. Eveleth, Jennifer J. Subramaniam, Amuthakannan Hahn, Rita Zhou, Peihong Gordon, Marion K. Bradshaw, Ralph A. An Engineered Human Fibroblast Growth Factor-1 Derivative, TTHX1114, Ameliorates Short-term Corneal Nitrogen Mustard Injury in Rabbit Organ Cultures |
title | An Engineered Human Fibroblast Growth Factor-1 Derivative, TTHX1114, Ameliorates Short-term Corneal Nitrogen Mustard Injury in Rabbit Organ Cultures |
title_full | An Engineered Human Fibroblast Growth Factor-1 Derivative, TTHX1114, Ameliorates Short-term Corneal Nitrogen Mustard Injury in Rabbit Organ Cultures |
title_fullStr | An Engineered Human Fibroblast Growth Factor-1 Derivative, TTHX1114, Ameliorates Short-term Corneal Nitrogen Mustard Injury in Rabbit Organ Cultures |
title_full_unstemmed | An Engineered Human Fibroblast Growth Factor-1 Derivative, TTHX1114, Ameliorates Short-term Corneal Nitrogen Mustard Injury in Rabbit Organ Cultures |
title_short | An Engineered Human Fibroblast Growth Factor-1 Derivative, TTHX1114, Ameliorates Short-term Corneal Nitrogen Mustard Injury in Rabbit Organ Cultures |
title_sort | engineered human fibroblast growth factor-1 derivative, tthx1114, ameliorates short-term corneal nitrogen mustard injury in rabbit organ cultures |
topic | Cornea |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155473/ https://www.ncbi.nlm.nih.gov/pubmed/30267094 http://dx.doi.org/10.1167/iovs.18-24568 |
work_keys_str_mv | AT evelethdavidd anengineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT evelethjenniferj anengineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT subramaniamamuthakannan anengineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT hahnrita anengineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT zhoupeihong anengineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT gordonmarionk anengineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT bradshawralpha anengineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT evelethdavidd engineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT evelethjenniferj engineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT subramaniamamuthakannan engineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT hahnrita engineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT zhoupeihong engineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT gordonmarionk engineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures AT bradshawralpha engineeredhumanfibroblastgrowthfactor1derivativetthx1114amelioratesshorttermcornealnitrogenmustardinjuryinrabbitorgancultures |