Department of Research and Development, Grupo Boticário, Biomolecular Research Laboratory, São José dos Pinhais, Paraná, Brazil.
Int J Cosmet Sci. 2013 Oct;35(5):448-57. doi: 10.1111/ics.12064. Epub 2013 Jun 27.
Stem cells have the ability to renew themselves and differentiate into various cell types. For this reason, numerous research groups have been studying these cells for their therapeutic potential. Some of the therapies, however, are not producing the expected results because of contamination by other cell types, especially by fibroblasts. In the cosmetic industry, stem cells are used to test the efficacy of anti-ageing and rejuvenation products. The purpose of this work was to gain a better understanding of the differences in phenotype, in gene expression associated with stem cells, in the pattern of cell surface proteins and in the differentiation capacity of adipose-derived stem cells, of skin-derived stem cells and of commercially available fibroblasts.
In this study, we compared fibroblasts with mesenchymal stem cells derived from bone marrow, skin (dermis) and adipose tissue, to assess the differentiation potential of fibroblasts. Dermal and adipose stem cells were isolated from aesthetic surgery patients, and fibroblasts were obtained from a commercial source. The following parameters were used in this study: immunophenotypic profile (positive: CD29, CD73, CD90 and CD105; negative: CD14, CD45 and HLA-DR); differentiation into osteoblastic, chondrogenic and adipogenic cell types; and PCR array to analyse the gene expression of cells isolated from different culture passages.
Fibroblasts express the same cell immunophenotypic markers, as well as the genes that are known to be expressed in stem cells, and were shown to be expressed also in adipose and dermis stem cells. Fibroblasts are also able to differentiate into the three cell lineages mentioned above, that is, adipocytes, osteocytes and chondrocytes.
Human dermal fibroblasts have a potential to adhere to plastic surfaces and differentiate into other cell types. However, for stem cells intended to be used in cosmetics, experiments conducted with contaminated fibroblasts may produce poor or even falsely negative results for the efficacy of the active ingredient or formulation and thus conceal their promising effects as anti-ageing and skin rejuvenation products.
干细胞具有自我更新和分化为多种细胞类型的能力。出于这个原因,许多研究小组一直在研究这些细胞的治疗潜力。然而,由于其他细胞类型的污染,特别是成纤维细胞的污染,一些疗法并没有产生预期的效果。在化妆品行业,干细胞被用于测试抗衰老和 rejuvenation 产品的功效。这项工作的目的是更好地了解脂肪来源干细胞、皮肤来源干细胞和商业上可用的成纤维细胞之间的表型、与干细胞相关的基因表达、细胞表面蛋白模式和分化能力的差异。
在这项研究中,我们比较了成纤维细胞与骨髓、皮肤(真皮)和脂肪组织来源的间充质干细胞,以评估成纤维细胞的分化潜力。真皮和脂肪干细胞从美容手术患者中分离,成纤维细胞从商业来源获得。本研究采用以下参数:免疫表型谱(阳性:CD29、CD73、CD90 和 CD105;阴性:CD14、CD45 和 HLA-DR);向成骨细胞、软骨细胞和成脂细胞分化;以及 PCR 阵列分析来自不同培养传代的细胞的基因表达。
成纤维细胞表达相同的细胞免疫表型标记物,以及已知在干细胞中表达的基因,并且也在脂肪和真皮干细胞中表达。成纤维细胞还能够分化为上述三种细胞谱系,即脂肪细胞、成骨细胞和软骨细胞。
人真皮成纤维细胞具有粘附于塑料表面并分化为其他细胞类型的潜力。然而,对于打算用于化妆品的干细胞,用污染的成纤维细胞进行的实验可能会对活性成分或制剂的功效产生较差甚至虚假的阴性结果,从而掩盖其作为抗衰老和皮肤 rejuvenation 产品的有前景的效果。