The role of fibroblast PPARβ/δ in skin homeostasis

The skin is the largest organ in the body and is made up of mainly the epidermis and dermis. The skin functions as a natural barrier against external stimuli, dehydration and injury. Peroxisome proliferator-activated receptor β/δ (PPARβ/δ) is one member of the PPAR family of nuclear receptors, and t...

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Main Author: Sng, Ming Keat
Other Authors: Tan Nguan Soon, Andrew
Format: Thesis
Language:English
Published: 2016
Subjects:
Online Access:https://hdl.handle.net/10356/66431
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author Sng, Ming Keat
author2 Tan Nguan Soon, Andrew
author_facet Tan Nguan Soon, Andrew
Sng, Ming Keat
author_sort Sng, Ming Keat
collection NTU
description The skin is the largest organ in the body and is made up of mainly the epidermis and dermis. The skin functions as a natural barrier against external stimuli, dehydration and injury. Peroxisome proliferator-activated receptor β/δ (PPARβ/δ) is one member of the PPAR family of nuclear receptors, and the predominant subtype found in the epidermis and dermis. Epidermal PPARβ/δ has well-established roles in maintaining skin homeostasis, such as during wound healing. However, in the mammalian system, skin homeostasis depends on a complex crosstalk between the epithelial and mesenchymal compartments, underscoring the importance for a tight regulation of the complex epiethelial-mesenchymal interaction. Although epidermal PPARβ/δ in normal wound healing is well-studied, there has been no progress in clinical therapies for diabetic chronic wounds. This is also ensued with problems such as drug bioavailability and patients’ compliance. In our study, we showed that pharmacological activation of fibroblasts PPARβ/δ activity using microencapsulated ligands can promote the healing of diabetic wounds via the modulation of ROS production. The role of PPARβ/δ in other diseases, such as cancer, has also been controversial due to differences in experimental setups and genetic modifications of the PPARβ/δ gene. While epidermal PPARβ/δ has been widely investigated on in these diseases, the role of fibroblasts PPARβ/δ in skin homeostasis and disease has been neglected. Hence, we generated a novel mouse model with the PPARβ/δ gene deleted specifically in the fibroblasts. These animal exhibited skin abnormalities during development, such as dermal thickening and increased collagen production, recapitulating a morphea-like phenotype. In addition, the dermis manifest as a hotbed for inflammatory events. In our subsequent preliminary studies, we showed that cancer-associated fibroblasts from squamous cell carcinoma exhibit low levels of PPARβ/δ. Our novel mouse model will therefore serve as an appropriate model to study the role of fibroblasts PPARβ/δ in diseases, such as acute inflammation, wound healing and tumorigenesis in the future.
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spelling ntu-10356/664312023-02-28T18:35:26Z The role of fibroblast PPARβ/δ in skin homeostasis Sng, Ming Keat Tan Nguan Soon, Andrew School of Biological Sciences DRNTU::Science::Biological sciences The skin is the largest organ in the body and is made up of mainly the epidermis and dermis. The skin functions as a natural barrier against external stimuli, dehydration and injury. Peroxisome proliferator-activated receptor β/δ (PPARβ/δ) is one member of the PPAR family of nuclear receptors, and the predominant subtype found in the epidermis and dermis. Epidermal PPARβ/δ has well-established roles in maintaining skin homeostasis, such as during wound healing. However, in the mammalian system, skin homeostasis depends on a complex crosstalk between the epithelial and mesenchymal compartments, underscoring the importance for a tight regulation of the complex epiethelial-mesenchymal interaction. Although epidermal PPARβ/δ in normal wound healing is well-studied, there has been no progress in clinical therapies for diabetic chronic wounds. This is also ensued with problems such as drug bioavailability and patients’ compliance. In our study, we showed that pharmacological activation of fibroblasts PPARβ/δ activity using microencapsulated ligands can promote the healing of diabetic wounds via the modulation of ROS production. The role of PPARβ/δ in other diseases, such as cancer, has also been controversial due to differences in experimental setups and genetic modifications of the PPARβ/δ gene. While epidermal PPARβ/δ has been widely investigated on in these diseases, the role of fibroblasts PPARβ/δ in skin homeostasis and disease has been neglected. Hence, we generated a novel mouse model with the PPARβ/δ gene deleted specifically in the fibroblasts. These animal exhibited skin abnormalities during development, such as dermal thickening and increased collagen production, recapitulating a morphea-like phenotype. In addition, the dermis manifest as a hotbed for inflammatory events. In our subsequent preliminary studies, we showed that cancer-associated fibroblasts from squamous cell carcinoma exhibit low levels of PPARβ/δ. Our novel mouse model will therefore serve as an appropriate model to study the role of fibroblasts PPARβ/δ in diseases, such as acute inflammation, wound healing and tumorigenesis in the future. DOCTOR OF PHILOSOPHY (SBS) 2016-04-05T08:01:44Z 2016-04-05T08:01:44Z 2016 Thesis Sng, M. K. (2016). The role of fibroblast PPARβ/δ in skin homeostasis. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/66431 10.32657/10356/66431 en 241 p. application/pdf
spellingShingle DRNTU::Science::Biological sciences
Sng, Ming Keat
The role of fibroblast PPARβ/δ in skin homeostasis
title The role of fibroblast PPARβ/δ in skin homeostasis
title_full The role of fibroblast PPARβ/δ in skin homeostasis
title_fullStr The role of fibroblast PPARβ/δ in skin homeostasis
title_full_unstemmed The role of fibroblast PPARβ/δ in skin homeostasis
title_short The role of fibroblast PPARβ/δ in skin homeostasis
title_sort role of fibroblast pparβ δ in skin homeostasis
topic DRNTU::Science::Biological sciences
url https://hdl.handle.net/10356/66431
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