The combination of DHEA, histamine, and insulin increases adipogenic differentiation and enhances tissue transplantation outcome in mice. (19th June 2013)
- Record Type:
- Journal Article
- Title:
- The combination of DHEA, histamine, and insulin increases adipogenic differentiation and enhances tissue transplantation outcome in mice. (19th June 2013)
- Main Title:
- The combination of DHEA, histamine, and insulin increases adipogenic differentiation and enhances tissue transplantation outcome in mice
- Authors:
- Park, Yoorim
Jung, Min Kyung
Yoon, Sun Young
Lee, Ha‐Reum
Hur, Dae Young
Kim, Daejin
Yang, Yoolhee
Kim, Tae Sung
Kim, Seonghan
Yoon, Suk Ran
Park, Hyun Jeong
Bang, Sa Ik
Cho, Dae Ho - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <p>Adipose stem cells (ASCs) are pluripotent cells that can generate pure fat tissue for regeneration. Differentiated adipose cells have been generated by a common inducer cocktail composed of dexamethasone, insulin, and isobutylmethylxanthine (DIM). The major drawbacks of adipose cells are their tendency to float on the culture media and their cost. To overcome some of these disadvantages, a new inducer cocktail that includes insulin, dehydroepiandrosterone, and histamine (D<sub>H</sub>IH) was tested. As a result, lipid accumulation was elevated more than twofold with D<sub>H</sub>IH than with DIM. Cell adhesion and viability, which are important factors for stable differentiation, were increased with D<sub>H</sub>IH and were proven through measurement of mRNA expression levels of adhesion marker genes, N‐cadherin and vascular cell adhesion molecule, as well as through an alamar blue assay. The expression of adipogenesis‐related genes, adiponectin, and glucose transporter type 4 lasted for a long time. To improve the efficiency of grafting, cell adhesion and neovascularization need to be increased. Neovascularization was observed around the transplanted adipose cells, which showed a higher number of vessel formation in D<sub>H</sub>IH than in DIM. The above results suggest that D<sub>H</sub>IH can produce pure differentiated adipose cells effectively and enhance their adhesion onto the target location when these<abstract abstract-type="main"> <title>Abstract</title> <p>Adipose stem cells (ASCs) are pluripotent cells that can generate pure fat tissue for regeneration. Differentiated adipose cells have been generated by a common inducer cocktail composed of dexamethasone, insulin, and isobutylmethylxanthine (DIM). The major drawbacks of adipose cells are their tendency to float on the culture media and their cost. To overcome some of these disadvantages, a new inducer cocktail that includes insulin, dehydroepiandrosterone, and histamine (D<sub>H</sub>IH) was tested. As a result, lipid accumulation was elevated more than twofold with D<sub>H</sub>IH than with DIM. Cell adhesion and viability, which are important factors for stable differentiation, were increased with D<sub>H</sub>IH and were proven through measurement of mRNA expression levels of adhesion marker genes, N‐cadherin and vascular cell adhesion molecule, as well as through an alamar blue assay. The expression of adipogenesis‐related genes, adiponectin, and glucose transporter type 4 lasted for a long time. To improve the efficiency of grafting, cell adhesion and neovascularization need to be increased. Neovascularization was observed around the transplanted adipose cells, which showed a higher number of vessel formation in D<sub>H</sub>IH than in DIM. The above results suggest that D<sub>H</sub>IH can produce pure differentiated adipose cells effectively and enhance their adhesion onto the target location when these differentiated adipose cells were applied as a clinical resource.</p> </abstract> … (more)
- Is Part Of:
- Biotechnology and applied biochemistry. Volume 60:Number 3(2013:May/Jun.)
- Journal:
- Biotechnology and applied biochemistry
- Issue:
- Volume 60:Number 3(2013:May/Jun.)
- Issue Display:
- Volume 60, Issue 3 (2013)
- Year:
- 2013
- Volume:
- 60
- Issue:
- 3
- Issue Sort Value:
- 2013-0060-0003-0000
- Page Start:
- 356
- Page End:
- 364
- Publication Date:
- 2013-06-19
- Subjects:
- Biotechnology -- Periodicals
Biochemical engineering -- Periodicals
Biochemistry -- Periodicals
Biochemistry -- Periodicals
Genetic Techniques -- Periodicals
Microbiological Techniques -- Periodicals
660.6 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1470-8744 ↗
http://www.babonline.org/ ↗
http://onlinelibrary.wiley.com/ ↗
http://bab.portlandpress.com/ ↗
http://bab.portlandpress.co.uk/ ↗ - DOI:
- 10.1002/bab.1100 ↗
- Languages:
- English
- ISSNs:
- 0885-4513
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2089.848000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3692.xml