Adipose stem cells controlled by surface chemistry. (12th December 2011)
- Record Type:
- Journal Article
- Title:
- Adipose stem cells controlled by surface chemistry. (12th December 2011)
- Main Title:
- Adipose stem cells controlled by surface chemistry
- Authors:
- Liu, Xi
He, Jin
Zhang, Shuming
Wang, Xiu‐Mei
Liu, Huan‐Ye
Cui, Fu‐Zhai - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <p>This study investigated how human adipose stem cells (hASCs) could be influenced by surface chemistry. Self‐assembled monolayers of alkanethiolates on gold were introduced as a surface chemistry model to provide a range of functional groups such as OH, COOH, NH<sub>2</sub>, Phenyl, SH, Br, and CH<sub>3</sub> on surfaces. Initially, morphological changes of hASCs in response to different surface chemistries were observed with focal adhesion. Cell growth behaviour evaluated by Cell Counting Kit‐8 (CCK8) assay (Dojindo Molecular Technologies Inc., Shanghai, China) and cytoskeletal F‐actin Biochem Kit™ (Denver, CO, USA) staining revealed a descending order of growth rate on the following surfaces: NH<sub>2</sub> &gt; SH &gt; COOH &gt; Phenyl &gt; Br &gt; OH &gt; CH<sub>3</sub>. The mRNA expressions of lineage specific markers including alkaline phosphatase (ALP), osteocalcin (OCN), type II collagen, aggrecan, peroxisome proliferator‐activated receptor gamma (PPAR<italic>γ</italic>), and fatty acid binding protein‐2 (aP2), were determined using real‐time reversed transcriptase‐polymerase chain reaction (RT‐PCR). Results revealed that NH<sub>2</sub> favoured hASC differentiation toward osteogenic, while phenyl and SH promoted chondrogenic differentiation of hASCs with a high level up‐regulation of type II collagen and aggrecan. hASCs on Br increased in PPAR<italic>γ</italic> and aP2 expression, indicating adipogenic<abstract abstract-type="main"> <title>Abstract</title> <p>This study investigated how human adipose stem cells (hASCs) could be influenced by surface chemistry. Self‐assembled monolayers of alkanethiolates on gold were introduced as a surface chemistry model to provide a range of functional groups such as OH, COOH, NH<sub>2</sub>, Phenyl, SH, Br, and CH<sub>3</sub> on surfaces. Initially, morphological changes of hASCs in response to different surface chemistries were observed with focal adhesion. Cell growth behaviour evaluated by Cell Counting Kit‐8 (CCK8) assay (Dojindo Molecular Technologies Inc., Shanghai, China) and cytoskeletal F‐actin Biochem Kit™ (Denver, CO, USA) staining revealed a descending order of growth rate on the following surfaces: NH<sub>2</sub> &gt; SH &gt; COOH &gt; Phenyl &gt; Br &gt; OH &gt; CH<sub>3</sub>. The mRNA expressions of lineage specific markers including alkaline phosphatase (ALP), osteocalcin (OCN), type II collagen, aggrecan, peroxisome proliferator‐activated receptor gamma (PPAR<italic>γ</italic>), and fatty acid binding protein‐2 (aP2), were determined using real‐time reversed transcriptase‐polymerase chain reaction (RT‐PCR). Results revealed that NH<sub>2</sub> favoured hASC differentiation toward osteogenic, while phenyl and SH promoted chondrogenic differentiation of hASCs with a high level up‐regulation of type II collagen and aggrecan. hASCs on Br increased in PPAR<italic>γ</italic> and aP2 expression, indicating adipogenic differentiation. These results highlight the vital role of surface chemistry on the modulation of hASC differentiation and suggests chemical methods for designing biomaterials for stem cell‐based tissue regeneration. Copyright © 2011 John Wiley &amp; Sons, Ltd.</p> </abstract> … (more)
- Is Part Of:
- Journal of tissue engineering and regenerative medicine. Volume 7:Number 2(2013:Feb.)
- Journal:
- Journal of tissue engineering and regenerative medicine
- Issue:
- Volume 7:Number 2(2013:Feb.)
- Issue Display:
- Volume 7, Issue 2 (2013)
- Year:
- 2013
- Volume:
- 7
- Issue:
- 2
- Issue Sort Value:
- 2013-0007-0002-0000
- Page Start:
- 112
- Page End:
- 117
- Publication Date:
- 2011-12-12
- Subjects:
- Tissue engineering -- Periodicals
Regeneration (Biology) -- Periodicals
610.28 - Journal URLs:
- https://www.hindawi.com/journals/jterm/journal-report/?utm_source=google&utm_medium=cpc&utm_campaign=HDW_MRKT_GBL_SUB_ADWO_PAI_DYNA_JOUR_X_X0000_WileyFlipsBatch4&gclid=EAIaIQobChMIm9PnxrmL_wIVibnVCh2F4we9EAAYASAAEgI0tvD_BwE ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/term.498 ↗
- Languages:
- English
- ISSNs:
- 1932-6254
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5069.508000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3556.xml