Genetic correction of Werner syndrome gene reveals impaired pro‐angiogenic function and HGF insufficiency in mesenchymal stem cells. Issue 5 (22nd April 2020)
- Record Type:
- Journal Article
- Title:
- Genetic correction of Werner syndrome gene reveals impaired pro‐angiogenic function and HGF insufficiency in mesenchymal stem cells. Issue 5 (22nd April 2020)
- Main Title:
- Genetic correction of Werner syndrome gene reveals impaired pro‐angiogenic function and HGF insufficiency in mesenchymal stem cells
- Authors:
- Tu, Jiajie
Wan, Chao
Zhang, Fengjie
Cao, Lianbao
Law, Patrick Wai Nok
Tian, Yuyao
Lu, Gang
Rennert, Owen M.
Chan, Wai‐Yee
Cheung, Hoi‐Hung - Abstract:
- Abstract: WRN mutation causes a premature aging disease called Werner syndrome (WS). However, the mechanism by which WRN loss leads to progeroid features evident with impaired tissue repair and regeneration remains unclear. To determine this mechanism, we performed gene editing in reprogrammed induced pluripotent stem cells (iPSCs) derived from WS fibroblasts. Gene correction restored the expression of WRN. WRN +/+ mesenchymal stem cells (MSCs) exhibited improved pro‐angiogenesis. An analysis of paracrine factors revealed that hepatocyte growth factor (HGF) was downregulated in WRN −/− MSCs. HGF insufficiency resulted in poor angiogenesis and cutaneous wound healing. Furthermore, HGF was partially regulated by PI3K/AKT signaling, which was desensitized in WRN −/− MSCs. Consistently, the inhibition of the PI3K/AKT pathway in WRN +/+ MSC resulted in reduced angiogenesis and poor wound healing. Our findings indicate that the impairment in the pro‐angiogenic function of WS‐MSCs is due to HGF insufficiency and PI3K/AKT dysregulation, suggesting trophic disruption between stromal and epithelial cells as a mechanism for WS pathogenesis. Abstract : Through correction of the Werner syndrome (WS) causative gene WRN, the paper reports a mechanism of HGF insufficiency in WS MSC and its connection with the impaired pro‐angiogenesis function. PI3K/AKT is the downregulated pathway in WS MSC.
- Is Part Of:
- Aging cell. Volume 19:Issue 5(2020)
- Journal:
- Aging cell
- Issue:
- Volume 19:Issue 5(2020)
- Issue Display:
- Volume 19, Issue 5 (2020)
- Year:
- 2020
- Volume:
- 19
- Issue:
- 5
- Issue Sort Value:
- 2020-0019-0005-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2020-04-22
- Subjects:
- WRN -- Werner syndrome -- HGF -- angiogenesis -- PI3K/AKT -- iPSC
Cells -- Aging -- Periodicals
571.8783605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1474-9726 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/acel.13116 ↗
- Languages:
- English
- ISSNs:
- 1474-9718
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0736.360500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 23371.xml