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Delayed Wound Healing in Heat Stable Antigen (HSA/CD24)-Deficient Mice
BACKGROUND: Healthy individuals rarely have problems with wound healing. Most skin lesions heal rapidly and efficiently within one to two weeks. However, many medical and surgical complications can be attributed to deficiencies in wound repair. Open wounds have lost the barrier that protects tissues...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594912/ https://www.ncbi.nlm.nih.gov/pubmed/26440795 http://dx.doi.org/10.1371/journal.pone.0139787 |
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author | Shapira, Shiran Ben-Amotz, Oded Sher, Osnat Kazanov, Dina Mashiah, Jacob Kraus, Sarah Gur, Eyal Arber, Nadir |
author_facet | Shapira, Shiran Ben-Amotz, Oded Sher, Osnat Kazanov, Dina Mashiah, Jacob Kraus, Sarah Gur, Eyal Arber, Nadir |
author_sort | Shapira, Shiran |
collection | PubMed |
description | BACKGROUND: Healthy individuals rarely have problems with wound healing. Most skin lesions heal rapidly and efficiently within one to two weeks. However, many medical and surgical complications can be attributed to deficiencies in wound repair. Open wounds have lost the barrier that protects tissues from bacterial invasion and allows the escape of vital fluids. Without expeditious healing, infections become more frequent. The CD24 gene encodes a heavily-glycosylated cell surface protein anchored to the membrane by phosphatidylinositol. CD24 plays an important role in the adaptive immune response and controls an important genetic checkpoint for homeostasis and autoimmune diseases in both mice and humans. We have previously shown that overexpression of CD24 results in increased proliferation and migration rates. AIM: To examine the role of CD24 in the wound healing process. METHODS: An excisional model of wound healing was used and delayed wound healing was studied in genetically modified heat stable antigen (HSA/CD24)-deficient mice (HSA (-/-)) compared to wild-type (WT) mice. RESULTS: Large full-thickness skin wounds, excised on the back of mice, exhibited a significant delay in the formation of granulation tissue, and in wound closure when compared to their WTHSA (+/+) littermates. Wounds were histologically analyzed and scored, based on the degree of cellular invasion, granulation tissue formation, vascularity, and re-epithelialization. Additionally, in stitched wounds, the HSA (-/-) mice failed to maintain their stitches; they did not hold and fell already 24 hours, revealing erythematous wound fields. Re-expression of HSA, delivered by lentivirus, restored the normal healing phenotype, within 24 hours post-injury, and even improved the healing in WT, and in BalbC mice. CONCLUSIONS: Delayed wound-healing in the absence of HSA/CD24 suggests that CD24 plays an important role in this process. Increased expression of CD24, even in the normal state, may be used to enhance wound repair. |
format | Online Article Text |
id | pubmed-4594912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45949122015-10-09 Delayed Wound Healing in Heat Stable Antigen (HSA/CD24)-Deficient Mice Shapira, Shiran Ben-Amotz, Oded Sher, Osnat Kazanov, Dina Mashiah, Jacob Kraus, Sarah Gur, Eyal Arber, Nadir PLoS One Research Article BACKGROUND: Healthy individuals rarely have problems with wound healing. Most skin lesions heal rapidly and efficiently within one to two weeks. However, many medical and surgical complications can be attributed to deficiencies in wound repair. Open wounds have lost the barrier that protects tissues from bacterial invasion and allows the escape of vital fluids. Without expeditious healing, infections become more frequent. The CD24 gene encodes a heavily-glycosylated cell surface protein anchored to the membrane by phosphatidylinositol. CD24 plays an important role in the adaptive immune response and controls an important genetic checkpoint for homeostasis and autoimmune diseases in both mice and humans. We have previously shown that overexpression of CD24 results in increased proliferation and migration rates. AIM: To examine the role of CD24 in the wound healing process. METHODS: An excisional model of wound healing was used and delayed wound healing was studied in genetically modified heat stable antigen (HSA/CD24)-deficient mice (HSA (-/-)) compared to wild-type (WT) mice. RESULTS: Large full-thickness skin wounds, excised on the back of mice, exhibited a significant delay in the formation of granulation tissue, and in wound closure when compared to their WTHSA (+/+) littermates. Wounds were histologically analyzed and scored, based on the degree of cellular invasion, granulation tissue formation, vascularity, and re-epithelialization. Additionally, in stitched wounds, the HSA (-/-) mice failed to maintain their stitches; they did not hold and fell already 24 hours, revealing erythematous wound fields. Re-expression of HSA, delivered by lentivirus, restored the normal healing phenotype, within 24 hours post-injury, and even improved the healing in WT, and in BalbC mice. CONCLUSIONS: Delayed wound-healing in the absence of HSA/CD24 suggests that CD24 plays an important role in this process. Increased expression of CD24, even in the normal state, may be used to enhance wound repair. Public Library of Science 2015-10-06 /pmc/articles/PMC4594912/ /pubmed/26440795 http://dx.doi.org/10.1371/journal.pone.0139787 Text en © 2015 Shapira et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Shapira, Shiran Ben-Amotz, Oded Sher, Osnat Kazanov, Dina Mashiah, Jacob Kraus, Sarah Gur, Eyal Arber, Nadir Delayed Wound Healing in Heat Stable Antigen (HSA/CD24)-Deficient Mice |
title | Delayed Wound Healing in Heat Stable Antigen (HSA/CD24)-Deficient Mice |
title_full | Delayed Wound Healing in Heat Stable Antigen (HSA/CD24)-Deficient Mice |
title_fullStr | Delayed Wound Healing in Heat Stable Antigen (HSA/CD24)-Deficient Mice |
title_full_unstemmed | Delayed Wound Healing in Heat Stable Antigen (HSA/CD24)-Deficient Mice |
title_short | Delayed Wound Healing in Heat Stable Antigen (HSA/CD24)-Deficient Mice |
title_sort | delayed wound healing in heat stable antigen (hsa/cd24)-deficient mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594912/ https://www.ncbi.nlm.nih.gov/pubmed/26440795 http://dx.doi.org/10.1371/journal.pone.0139787 |
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