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Liu et al.                                                                                                                                                                                Adipogenesis of obital fat stem cells

                        A                                     B
















                        C                                     D
















           Figure 3: Adipogenic differentiation was assessed by oil red O staining after culturing orbital adipose-derived stem cells in adipogenic
           media for 14 days. (A, C): young group; (B, D): middle-aged group; (A, B): non-induced; (C, D): induced. More positive staining cells were
           observed in (A, C) than those in (B, D), and almost no staining was seen in (A, B) (scale bar: 100 µm)
                     A                               Induced  B                                Induced
                                                     Non-induced                               Non-induced













           Figure 4: Quantitative analysis confirmed the adipogenic differentiation of orbital adipose-derived stem cells in contrast with the non-
           induced cells. Compared to the young age group, both the percentage of oil red O staining-positive cells (A) and the expression level of
           peroxisome proliferator-activated receptor γ mRNA (B) were significantly reduced in the middle-aged group (*P < 0.001)

           OF is derived from both mesodermal and ectodermal   of septal structure correlated with age were predicted,
           cells. [13]  The central fat pads of both upper and lower   and were attributable to OF herniation, resulting in a
           lids are mesodermally derived, while the medial fat in   baggy-eye appearance. Irregular and decreased fat cell
           the upper and lower eyelids develops from the neural   size at middle age may indicate the reduced capacity
           crest cells. [4,5]  Therefore, to achieve consistency   to accumulate lipid and reserve energy. [14]
           between groups, all samples used in this study were
           taken from the central fat compartments of the lower   Next, OASCs were isolated and expanded in vitro. The
           eyelids.                                           cell phenotype was characterized by flow cytometry,
                                                              and the effects of age on the number of OASCs’, their
           At the histological level, the fibrous septum surrounding   proliferation, and differentiation were investigated.
           the fat lobules was thin and sparse in the middle-aged   OASCs from both groups expressed a similar CD
           group, and the loosely arranged adipocytes appeared   marker profile, which was consistent with that reported
           smaller than those in the younger age group. Changes   for ASCs from SF depots. Although the viable cells

            326                                                                                       Plastic and Aesthetic Research ¦ Volume 3 ¦ October 25, 2016
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