A novel method for the isolation of sub-populations of Rat Adipose Stem Cells with different proliferation and osteogenic differentiation potentials

last updated: 2017-03-07
TitleA novel method for the isolation of sub-populations of Rat Adipose Stem Cells with different proliferation and osteogenic differentiation potentials
Publication TypePapers in Scientific Journals
Year of Publication2011
AuthorsRada T., Reis R. L., and Gomes M. E.
Abstract

and cartilage tissue-engineering approaches. Recent studies indicate that adipose tissue presents
significant advantages over bone marrow as a cell source for tissue engineering. Most of these
studies report the use of adipose stem cells (ASCs) isolated by a method based on the enzymatic
digestion of the adipose tissue and on the ability of stem cells to adhere to a cell culture plastic
surface. Using this method, a heterogeneous population was obtained containing different cell
types that have been shown to compromise the proliferation and differentiation potential of the
stem cells. This paper reports the development and optimization of a new isolation method that
enables purified cell populations to be obtained that exhibit higher osteogenic differentiation
and/or proliferation potential. This method is based on the use of immunomagnetic beads coated
with specific antibodies and it is compared with other methods described in the literature for
the selection of stem cell populations, e.g. methods based on a gradient solution and enzymatic
digestion. The results showed that the isolation method based on immunomagnetic beads allows
distinct subpopulations of rat ASCs to be isolated, showing different stem cells marker expressions
and different osteogenic differentiation potentials. Therefore, this method can be used to study
niches in ASC populations and/or also allow adipose tissue to be used as a stem cell source in a
more efficient manner, increasing the potential of this cell source in future clinical applications.

JournalTissue Engineering and Regenerative Medicine, DOI: 10.1002/term.364
Date Published2011-07-15
Keywordsadult stem cells, mesenchymal stem cells
RightsopenAccess
Peer reviewedno
Statuspublished

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