کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2816722 1159950 2014 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Variable expression of lineage regulators in differentiated stromal cells indicates distinct mechanisms of differentiation towards common cell fate
ترجمه فارسی عنوان
بیان متغیر رگولاتورهای خطوط در سلول های استرومایی متمایز نشان می دهد که مکانیزم های متمایز تمایز به سرنوشت سلولی مشترک است
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی ژنتیک
چکیده انگلیسی


• 14 stromal cell populations analyzed exhibit multipotency.
• Variable expression of lineage genes despite similar differentiation potential.
• Cell-to-cell variation of expression of lineage regulators.
• Unsimultaneous expression of lineage regulators in single cells.

Mesenchymal stem cells (MSCs) possess a multi-lineage differentiation capacity that makes them important players in the field of regenerative medicine. MSC populations derived from different tissues or donors have been shown to exhibit variable gene expression patterns. Further, it is widely acknowledged that MSC isolates are heterogeneous mixtures of cells at different developmental stages. However, the heterogeneity of expression of lineage regulators has not been linked to differentiation potential of different MSC populations towards mesenchymal lineages. Here, we analyzed variation of expression of differentiation markers across whole population and between single differentiating cells of multipotent stromal cell populations derived from adipose tissue (AdMSCs) and skin (FBs) of seven donors. The results of the analyses show that all cell populations exhibit similar differentiation potential towards adipocyte, osteoblast and chondrocyte lineages despite tissue type- and donor-specific variations of expression of differentiation-associated genes. Further, we detected variable expression of lineage regulators in individual differentiating cells. Together, our data indicate that single cells of stromal cell populations could use distinct molecular mechanisms to reach a common cell fate.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gene - Volume 533, Issue 1, 1 January 2014, Pages 173–179
نویسندگان
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