Literature DB >> 17518688

Effects of glutamine, glucose, and oxygen concentration on the metabolism and proliferation of rabbit adipose-derived stem cells.

K E Follmar1, F C Decroos, H L Prichard, H T Wang, D Erdmann, K C Olbrich.   

Abstract

The use of adipose-derived stem cells (ASCs) for tissue engineering involves exposing them to metabolically adverse conditions. This study examined the metabolism, proliferation, and viability of ASCs under various oxygen, glucose, and glutamine concentrations to determine how these cells respond to such environments. ASCs were cultured in each of 8 media preparations containing 4.8 or 21.5 mM glucose, and 0, 2, 4, or 6 mM glutamine. The ASCs were cultured under normoxic (20% O(2)) and hypoxic (0.1% O(2)) conditions. Conditioned media were collected and assayed for glucose, glutamine, lactate, pyruvate, and glutamate. Cell proliferation and cell death were measured after 5 days of culture. ASCs remained metabolically active under all culture conditions; however, their proliferation rate was significantly reduced in the absence of glutamine. Hypoxia resulted in increased cell death. ASCs are a viable source of stem cells for tissue engineering purposes, although substantial challenges remain. These cells are able to survive in environments with limited oxygen and glutamine and thus may be able to survive brief periods of limited nutrient transport after implantation.

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Year:  2006        PMID: 17518688     DOI: 10.1089/ten.2006.12.3525

Source DB:  PubMed          Journal:  Tissue Eng        ISSN: 1076-3279


  16 in total

Review 1.  The potential of adipose stem cells in regenerative medicine.

Authors:  Bettina Lindroos; Riitta Suuronen; Susanna Miettinen
Journal:  Stem Cell Rev Rep       Date:  2011-06       Impact factor: 5.739

Review 2.  Osteogenesis of Adipose-Derived Stem Cells.

Authors:  Brian E Grottkau; Yunfeng Lin
Journal:  Bone Res       Date:  2013-06-28       Impact factor: 13.567

Review 3.  The multiparametric effects of hydrodynamic environments on stem cell culture.

Authors:  Melissa A Kinney; Carolyn Y Sargent; Todd C McDevitt
Journal:  Tissue Eng Part B Rev       Date:  2011-05-25       Impact factor: 6.389

4.  Hypoxia and amino acid supplementation synergistically promote the osteogenesis of human mesenchymal stem cells on silk protein scaffolds.

Authors:  Sejuti Sengupta; Sang-Hyug Park; Atur Patel; Julia Carn; Kyongbum Lee; David L Kaplan
Journal:  Tissue Eng Part A       Date:  2010-09-01       Impact factor: 3.845

5.  Relationships between degradability of silk scaffolds and osteogenesis.

Authors:  Sang-Hyug Park; Eun Seok Gil; Hyeon Joo Kim; Kyongbum Lee; David L Kaplan
Journal:  Biomaterials       Date:  2010-08       Impact factor: 12.479

Review 6.  The role of hypoxia in stem cell differentiation and therapeutics.

Authors:  Hamid Abdollahi; Lisa J Harris; Ping Zhang; Stephen McIlhenny; Vikram Srinivas; Thomas Tulenko; Paul J DiMuzio
Journal:  J Surg Res       Date:  2009-10-24       Impact factor: 2.192

7.  Effects of hypoxic culture conditions on umbilical cord-derived human mesenchymal stem cells.

Authors:  Antonina Lavrentieva; Ingrida Majore; Cornelia Kasper; Ralf Hass
Journal:  Cell Commun Signal       Date:  2010-07-16       Impact factor: 5.712

8.  Functional binding of human adipose-derived stromal cells: effects of extraction method and hypoxia pretreatment.

Authors:  Peter J Amos; Alexander M Bailey; Hulan Shang; Adam J Katz; Michael B Lawrence; Shayn M Peirce
Journal:  Ann Plast Surg       Date:  2008-04       Impact factor: 1.539

9.  Use of adipose stem cells and polylactide discs for tissue engineering of the temporomandibular joint disc.

Authors:  Katja Mäenpää; Ville Ellä; Jari Mauno; Minna Kellomäki; Riitta Suuronen; Timo Ylikomi; Susanna Miettinen
Journal:  J R Soc Interface       Date:  2009-05-27       Impact factor: 4.118

10.  Buccal Fat Pad-Derived Stem Cells for Repair of Maxillofacial Bony Defects.

Authors:  Mitsu Meshram; Sonal Anchlia; Harsh Shah; Siddharth Vyas; Jigar Dhuvad; Lalit Sagarka
Journal:  J Maxillofac Oral Surg       Date:  2018-03-29
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