کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2094029 1081987 2016 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Genome-wide analysis of gene expression during adipogenesis in human adipose-derived stromal cells reveals novel patterns of gene expression during adipocyte differentiation
ترجمه فارسی عنوان
تجزیه و تحلیل ژن از بیان ژن در طی آدیپوژنز در سلول های استرومایی حاصل از چربی انسان نشانگر الگوهای نوین بیان ژن در زمان تمایز آدیپوسیت است
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوتکنولوژی یا زیست‌فناوری
چکیده انگلیسی


• A unique comprehensive transcriptomic study on adipogenesis in human ASCs
• Novel genes and transcription factors involved in adipogenesis were identified.
• Adipogenesis linked to neural and blood vessel development
• Identification of marker genes which characterise adipogenesis

We have undertaken an in-depth transcriptome analysis of adipogenesis in human adipose-derived stromal cells (ASCs) induced to differentiate into adipocytes in vitro. Gene expression was assessed on days 1, 7, 14 and 21 post-induction and genes differentially expressed numbered 128, 218, 253 and 240 respectively. Up-regulated genes were associated with blood vessel development, leukocyte migration, as well as tumor growth, invasion and metastasis. They also shared common pathways with certain obesity-related pathophysiological conditions. Down-regulated genes were enriched for immune response processes. KLF15, LMO3, FOXO1 and ZBTB16 transcription factors were up-regulated throughout the differentiation process. CEBPA, PPARG, ZNF117, MLXIPL, MMP3 and RORB were up-regulated only on days 14 and 21, which coincide with the maturation of adipocytes and could possibly serve as candidates for controlling fat accumulation and the size of mature adipocytes. In summary, we have identified genes that were up-regulated only on days 1 and 7 or days 14 and 21 that could serve as potential early and late-stage differentiation markers.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Stem Cell Research - Volume 16, Issue 3, May 2016, Pages 725–734
نویسندگان
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