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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Characterization of Equine Adipose Tissue-Derived Progenitor Cells Before and After Cryopreservation

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Author(s):
Mambelli, Lisley I. [1] ; Santos, Enrico J. C. [1, 2] ; Frazao, Paulo J. R. [3] ; Chaparro, Mariana B. [3] ; Kerkis, Alexandre [2] ; Zoppa, Andre L. V. [3] ; Kerkis, Irina [1]
Total Authors: 7
Affiliation:
[1] Butantan Inst, Genet Lab, Sao Paulo - Brazil
[2] Vet Activ Ltda, Appl Genet, Sao Paulo - Brazil
[3] Univ Sao Paulo, Dept Surg, Sch Vet Med & Anim Sci, Sao Paulo - Brazil
Total Affiliations: 3
Document type: Journal article
Source: TISSUE ENGINEERING PART C-METHODS; v. 15, n. 1, p. 87-94, MAR 2009.
Web of Science Citations: 46
Abstract

In horses, stem cell therapies are a promising tool to the treatment of many injuries, which are common consequences of athletic endeavor, resulting in high morbidity and often compromising the performance. In spite of many advantages, the isolation of stem cells similar to human, from equine adipose tissue, occurred only recently. The aim of this study was to isolate equine adipose tissue-derived progenitor cells (eAT-PC), to characterize their proliferative potential, and to study their differentiation capacity before and after cryopreservation. The cells, isolated from horse adipose tissue, presented similar fibroblast-like cell morphology in vitro. Their proliferation rate was evaluated during 63 days (23 passages) before and after cryopreservation. After the induction of osteogenic differentiation, von Kossa staining and positive immunostaining studies revealed the formation of calcified extracellular matrix confirming the osteogenic potential of these cells. Adipogenic differentiation was induced using two protocols: routine and other one developed by us, while our protocol requires a shorter time (Oil Red O staining revealed significant accumulation of lipid droplets after 7 days). Chondrogenic differentiation was observed after 21 days of induced pellet culture, as evidenced by histological (toluidine blue) and immunohistochemistry studies. Our data demonstrate that eAT-PC can be easily isolated and successfully expanded in vitro while presenting significant proliferating rate. These cells can be maintained undifferentiated in vitro and can efficiently undergo differentiation at least into mesodermal derivates. These eAT-PC properties were preserved even after cryopreservation. Our findings classify eAT-PC as a promising type of progenitor cells that can be applied in different cell therapies in equines. (AU)