Comparison of Markers and Functional Attributes of Human Adipose-Derived Stem Cells and Dedifferentiated Adipocyte Cells from Subcutaneous Fat of an Obese Diabetic Donor

被引:32
|
作者
Watson, James E. [1 ]
Patel, Niketa A. [1 ,2 ]
Carter, Gay [1 ]
Moor, Andrea [3 ]
Patel, Rekha [2 ]
Ghansah, Tomar [2 ]
Mathur, Abhishek [3 ]
Murr, Michel M. [3 ]
Bickford, Paula [1 ,4 ]
Gould, Lisa J. [1 ,3 ]
Cooper, Denise R. [1 ,2 ]
机构
[1] James A Haley Vet Hosp, Res Serv, Tampa, FL USA
[2] Univ S Florida, Dept Mol Med, Morsani Coll Med, Tampa, FL USA
[3] Univ S Florida, Dept Surg, Morsani Coll Med, Tampa, FL 33620 USA
[4] Univ S Florida, Dept Neurosurg, Morsani Coll Med, Tampa, FL 33620 USA
关键词
D O I
10.1089/wound.2013.0452
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Objective: Adipose tissue is a robust source of adipose-derived stem cells (ADSCs) that may be able to provide secreted factors that promote the ability of wounded tissue to heal. However, adipocytes also have the potential to dedifferentiate in culture to cells with stem cell-like properties that may improve their behavior and functionality for certain applications. Approach: ADSCs are adult mesenchymal stem cells that are cultured from the stromal vascular fraction of adipose tissue. However, adipocytes are capable of dedifferentiating into cells with stem cell properties. In this case study, we compare ADSC and dedifferentiated fat (DFAT) cells from the same patient and fat depot for mesenchymal cell markers, embryonic stem cell markers, ability to differentiate to adipocytes and osteoblasts, senescence and telomerase levels, and ability of conditioned media (CM) to stimulate migration of human dermal fibroblasts (HDFs). Innovation and Conclusions: ADSCs and DFAT cells displayed identical levels of CD90, CD44, CD105, and were CD34-and CD45-negative. They also expressed similar levels of Oct4, BMI1, KLF4, and SALL4. DFAT cells, however, showed higher efficiency in adipogenic and osteogenic capacity. Telomerase levels of DFAT cells were double those of ADSCs, and senescence declined in DFAT cells. CM from both cell types altered the migration of fibroblasts. Despite reports of ADSCs from a number of human depots, there have been no comparisons of the ability of dedifferentiated DFAT cells from the same donor and depot to differentiate or modulate migration of HDFs. Since ADSCs were from an obese diabetic donor, reprogramming of DFAT cells may help improve a patient's cells for regenerative medicine applications.
引用
收藏
页码:219 / 228
页数:10
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