Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/38273
Title: Cell kinetics, DNA integrity, differentiation, and lipid fingerprinting analysis of rabbit adipose-derived stem cells
Authors: Sa Barretto, Leticia Siqueira de [UNIFESP]
Lessio, Camila [UNIFESP]
Sawaki e Nakamura, Ahy Natally [UNIFESP]
Lo Turco, Edson Guimaraes [UNIFESP]
Silva, Camila Gonzaga da [UNIFESP]
Zambon, Joao Paulo [UNIFESP]
Gozzo, Fabio Cesar
Pilau, Eduardo Jorge
Almeida, Fernando Goncalves de [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Universidade Estadual de Campinas (UNICAMP)
Keywords: Adipose-derived stem cells
Rabbit
DNA integrity
Lipid fingerprinting analysis
Animal model
Issue Date: 1-Oct-2014
Publisher: Springer
Citation: In Vitro Cellular & Developmental Biology-animal. New York: Springer, v. 50, n. 9, p. 831-839, 2014.
Abstract: Human adipose tissue has been described as a potential alternative reservoir for stem cells. Although studies have been performed in rabbits using autologous adipose-derived stem cells (ADSC), these cells have not been well characterized. the primary objectives of this study were to demonstrate the presence of adipose-derived stem cells isolated from rabbit inguinal fat pads and to characterize them through osteogenic and adipogenic in vitro differentiation and lipid fingerprinting analysis. the secondary objective was to evaluate cell behavior through growth kinetics, cell viability, and DNA integrity. Rabbit ADSCs were isolated to determine the in vitro growth kinetics and cell viability. DNA integrity was assessed by an alkaline Comet assay in passages 0 and 5. the osteogenic differentiation was evaluated by Von Kossa, and Alizarin Red S staining and adipogenic differentiation were assessed by Oil Red O staining. Lipid fingerprinting analyses of control, adipogenic, and osteogenic differentiated cells were performed by MALDI-TOF/MS. We demonstrate that rabbit ADSC have a constant growth rate at the early passages, with increased DNA fragmentation at or after passage 5. Rabbit ADSC viability was similar in passages 2 and 5 (90.7% and 86.6%, respectively), but there was a tendency to decreased cellular growth rate after passage 3. the ADSC were characterized by the expression of surface markers such as CD29 (67.4%) and CD44 (89.4%), using CD 45 (0.77%) as a negative control. ADSC from rabbits were successfully isolated form the inguinal region. These cells were capable to differentiate into osteogenic and adipogenic tissue when they were placed in inductive media. After each passage, there was a trend towards decreased cell growth. On the other hand, DNA fragmentation increased at each passage. ADSC had a different lipid profile when placed in control, adipogenic, or osteogenic media.
URI: http://repositorio.unifesp.br/handle/11600/38273
ISSN: 1071-2690
Other Identifiers: http://dx.doi.org/10.1007/s11626-014-9782-x
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