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Metabolic and functional characterization of human adipose-derived stem cells in tissue engineering.

Publication ,  Journal Article
Mischen, BT; Follmar, KE; Moyer, KE; Buehrer, B; Olbrich, KC; Levin, LS; Klitzman, B; Erdmann, D
Published in: Plast Reconstr Surg
September 2008

BACKGROUND: The use of adipose-derived stem cells for tissue engineering involves exposing them to metabolically adverse conditions. This study examines the metabolism, proliferation, and differentiation of adipose-derived stem cells under various conditions. METHODS: Adipose-derived stem cells were cultured in 16 media conditions containing 0.6, 2.4, 4.3, or 6.1 mM glucose; 0.1, 2.5, 4.1, or 6.1 mM glutamine; and then grown in either 0.1% or 20% oxygen. Conditioned media were collected and assayed for glucose, lactate, and pyruvate. Cell proliferation and cell death were measured at several time points. Osteogenic differentiation was analyzed by alizarin red staining/quantification and alkaline phosphatase activity, measured weekly over 4 weeks. RESULTS: Adipose-derived stem cells remained metabolically active in all nutrient and oxygen conditions tested. Glucose consumption and lactate production increased under hypoxic conditions, but pyruvate consumption was jointly dependent on oxygen and glucose concentration. The 20% oxygen environment produced greater proliferation and cell death compared with the hypoxic environment. Osteogenic differentiation of adipose-derived stem cells was observed only when glucose and/or oxygen concentrations were physiologically normal to high. CONCLUSIONS: Adipose-derived stem cells are an excellent source of multipotent cells and are capable of advancing current tissue engineering methodologies. These data show that adipose-derived stem cells remain viable under adverse conditions of low glucose, glutamine, and oxygen concentrations. However, there are variable levels of differentiation in the various culture conditions, which could lead to challenges in de novo osteogenesis and other forms of tissue engineering. Therefore, these results should be used in developing specific strategies to ensure successful application of adipose-derived stem cells in bone engineering and similar applications.

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Published In

Plast Reconstr Surg

DOI

EISSN

1529-4242

Publication Date

September 2008

Volume

122

Issue

3

Start / End Page

725 / 738

Location

United States

Related Subject Headings

  • Tissue and Organ Harvesting
  • Tissue Engineering
  • Surgery
  • Pyruvic Acid
  • Multipotent Stem Cells
  • Lactic Acid
  • Humans
  • Glucose
  • Cells, Cultured
  • Cell Division
 

Citation

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Mischen, B. T., Follmar, K. E., Moyer, K. E., Buehrer, B., Olbrich, K. C., Levin, L. S., … Erdmann, D. (2008). Metabolic and functional characterization of human adipose-derived stem cells in tissue engineering. Plast Reconstr Surg, 122(3), 725–738. https://doi.org/10.1097/PRS.0b013e318180ec9f
Mischen, Blaine T., Keith E. Follmar, Kurtis E. Moyer, Ben Buehrer, Kevin C. Olbrich, L Scott Levin, Bruce Klitzman, and Detlev Erdmann. “Metabolic and functional characterization of human adipose-derived stem cells in tissue engineering.Plast Reconstr Surg 122, no. 3 (September 2008): 725–38. https://doi.org/10.1097/PRS.0b013e318180ec9f.
Mischen BT, Follmar KE, Moyer KE, Buehrer B, Olbrich KC, Levin LS, et al. Metabolic and functional characterization of human adipose-derived stem cells in tissue engineering. Plast Reconstr Surg. 2008 Sep;122(3):725–38.
Mischen, Blaine T., et al. “Metabolic and functional characterization of human adipose-derived stem cells in tissue engineering.Plast Reconstr Surg, vol. 122, no. 3, Sept. 2008, pp. 725–38. Pubmed, doi:10.1097/PRS.0b013e318180ec9f.
Mischen BT, Follmar KE, Moyer KE, Buehrer B, Olbrich KC, Levin LS, Klitzman B, Erdmann D. Metabolic and functional characterization of human adipose-derived stem cells in tissue engineering. Plast Reconstr Surg. 2008 Sep;122(3):725–738.

Published In

Plast Reconstr Surg

DOI

EISSN

1529-4242

Publication Date

September 2008

Volume

122

Issue

3

Start / End Page

725 / 738

Location

United States

Related Subject Headings

  • Tissue and Organ Harvesting
  • Tissue Engineering
  • Surgery
  • Pyruvic Acid
  • Multipotent Stem Cells
  • Lactic Acid
  • Humans
  • Glucose
  • Cells, Cultured
  • Cell Division