O084 Adipose-derived stem cells attenuate the induction of tissue destructive and inflammatory fibroblasts by ionising radiation. (22nd July 2022)
- Record Type:
- Journal Article
- Title:
- O084 Adipose-derived stem cells attenuate the induction of tissue destructive and inflammatory fibroblasts by ionising radiation. (22nd July 2022)
- Main Title:
- O084 Adipose-derived stem cells attenuate the induction of tissue destructive and inflammatory fibroblasts by ionising radiation
- Authors:
- Langridge, B J
Abu-Hannah, J
Carter, R
Butler, PEM - Abstract:
- Abstract: Introduction: Radiation-Induced Fibrosis (RIF) is a common complication of radiotherapy with no effective treatment, causing permanent, progressive disability and disfigurement of cancer patients. Autologous lipotransfer has promise as a treatment for RIF, with adipose-derived stem cells (ADSCs) proposed as the key effector mechanism. This study investigates the effects of ADSCs on irradiated human dermal fibroblasts (HDFs). Methods: HDFs ( n = 3), control or irradiated (10Gy), were grown in monoculture, co-culture with ADSCs or in the presence of ADSC-conditioned media (ADSC-CM) over a 2-week period. RT-PCR was used to determine the mRNA expression of 84 inflammatory and fibrotic genes. ELISA was used to measure the levels of MMP1, MMP3 and CCL2 secreted. Immunocytochemistry was used to stain HDFs for type 1 collagen and αSMA. Results: Compared to control HDFs, irradiated HDFs demonstrated reduced proliferation and upregulated the mRNA expression and protein secretion of multiple fibrotic and inflammatory genes, including MMP-1, MMP-3, IL-4 and CCL2. Accompanying upregulation of these genes was increased expression of fibroblast activation markers FAPA and PDPN and decreased expression of THY1. Coculture with ADSCs or ADSC-CM attenuated many of these effects. Conclusion: Ionising radiation promotes the generation of FAPα+THY1- tissue-destructive fibroblasts that secrete high levels of MMPs, degrading and restructuring the extracellular matrix of the skin. ElevatedAbstract: Introduction: Radiation-Induced Fibrosis (RIF) is a common complication of radiotherapy with no effective treatment, causing permanent, progressive disability and disfigurement of cancer patients. Autologous lipotransfer has promise as a treatment for RIF, with adipose-derived stem cells (ADSCs) proposed as the key effector mechanism. This study investigates the effects of ADSCs on irradiated human dermal fibroblasts (HDFs). Methods: HDFs ( n = 3), control or irradiated (10Gy), were grown in monoculture, co-culture with ADSCs or in the presence of ADSC-conditioned media (ADSC-CM) over a 2-week period. RT-PCR was used to determine the mRNA expression of 84 inflammatory and fibrotic genes. ELISA was used to measure the levels of MMP1, MMP3 and CCL2 secreted. Immunocytochemistry was used to stain HDFs for type 1 collagen and αSMA. Results: Compared to control HDFs, irradiated HDFs demonstrated reduced proliferation and upregulated the mRNA expression and protein secretion of multiple fibrotic and inflammatory genes, including MMP-1, MMP-3, IL-4 and CCL2. Accompanying upregulation of these genes was increased expression of fibroblast activation markers FAPA and PDPN and decreased expression of THY1. Coculture with ADSCs or ADSC-CM attenuated many of these effects. Conclusion: Ionising radiation promotes the generation of FAPα+THY1- tissue-destructive fibroblasts that secrete high levels of MMPs, degrading and restructuring the extracellular matrix of the skin. Elevated secretion of pro-inflammatory mediators CCL2 and IL-4, create a microenvironment permissive for the recruitment of monocytes and pro-fibrotic macrophages. ADSCs reverse many of the changes driven by ionising radiation, including the generation of tissue-destructive fibroblasts, through paracrine signalling. Take-home message: Ionising radiation promotes the generation of FAPα+THY1- tissue-destructive fibroblasts that secrete high levels of MMPs, degrading and restructuring the extracellular matrix of the skin. ADSCs can reverse many of the changes driven by ionising radiation, including the generation of tissue-destructive fibroblasts, through paracrine signalling. … (more)
- Is Part Of:
- British journal of surgery. Volume 109(2022)Supplement 4
- Journal:
- British journal of surgery
- Issue:
- Volume 109(2022)Supplement 4
- Issue Display:
- Volume 109, Issue 4 (2022)
- Year:
- 2022
- Volume:
- 109
- Issue:
- 4
- Issue Sort Value:
- 2022-0109-0004-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-07-22
- Subjects:
- Surgery -- Periodicals
617.005 - Journal URLs:
- http://www.bjs.co.uk/bjsCda/cda/microHome.do ↗
https://academic.oup.com/bjs# ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1093/bjs/znac242.084 ↗
- Languages:
- English
- ISSNs:
- 0007-1323
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2325.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22700.xml