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Home › Dataset Library › Gene-chip studies of adipogenesis-regulated microRNAs in mouse primary adipocytes and human obesity (Affymetrix)

Dataset: Gene-chip studies of adipogenesis-regulated microRNAs in mouse primary adipocytes and human obesity (Affymetrix)

Adipose tissue abundance relies partly on the factors that regulate adipogenesis, i.e. proliferation and differentiation of adipocytes....

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Adipose tissue abundance relies partly on the factors that regulate adipogenesis, i.e. proliferation and differentiation of adipocytes. While the transcriptional program that initiates adipogenesis is well-known, the importance of microRNAs in adipogenesis is less well studied. We thus set out to investigate whether miRNAs would be actively modulated during adipogenesis and obesity. Several models exist to study adipogenesis in vitro, of which the cell line 3T3-L1 is probably the most well known, albeit not the most physiologically appropriate. We used a microarray strategy to provide a global profile of miRNAs in brown and white primary murine adipocytes (prior to and following differentiation) and evaluated the similarity of the responses to non-primary cell models, through literature data-mining. We found 65 miRNAs regulated during in vitro adipogenesis in primary adipocytes. When we compared our primary adipocyte profiles with those of cell lines reported in the literature, we found a high degree of difference in adipogenesis-regulated miRNAs. We evaluated the expression of 10 of our adipogenesis-regulated miRNAs using real-time qPCR and then selected 5 miRNAs that showed robust expression levels and profiled these by qPCR in subcutaneous adipose tissue of 20 humans with a range of body mass indices (BMI, range=21-48). Of the miRNAs tested, mir-21 was both highly expressed in human adipose tissue and positively correlated with BMI (R2=0.49, p<0.001). In conclusion, we provide the preliminary analysis of miRNAs important for primary cell in vitro adipogenesis and find that the inflammation-associated miRNA, mir-21, is up-regulated in subcutaneous adipose tissue in human obesity. A global transcriptomic survey of subcutaneous adipose tissue from human subjects characterised as having normal glucose tolerance, glucose intolerance or frank type 2 diabetes.

Species:
human

Samples:
33

Source:
E-GEOD-27949

PubMed:
21426570

Updated:
Dec.12, 2014

Registered:
Sep.15, 2014


Factors: (via ArrayExpress)
Sample FASTING INSULIN CLINICAL STATUS VO2MAX FFM BMI FASTING GLUCOSE HBA1C AGE
GSM691122 117 NGT 41 38.1 5.2 5.5 22
GSM691123 37 NGT 27 35.3 4.5 5.5 48
GSM691124 62 NGT 72 32.9 5.0 5.7 39
GSM691125 67 DM 36 42.2 9.0 6.1 56
GSM691126 53 IGT 45 39.7 5.9 5.4 41
GSM691127 61 IGT 54 36.7 5.8 5.2 47
GSM691128 124 IGT 23 41.5 5.9 5.8 58
GSM691129 162 DM 27 50.2 6.9 6.2 49
GSM691130 52 NGT 39 37.4 4.5 5.9 46
GSM69113 59 NGT 47 36.7 5.0 5.7 45
GSM691132 118 IGT 38 39.5 6.2 6.2 57
GSM691133 36 DM 49 27.2 5.9 6.6 50
GSM691134 33 NGT 26 33.2 5.4 5.7 60
GSM691135 60 DM 30 25.1 9.2 6.5 60
GSM691136 61 DM 46 23.2 9.5 8.4 55
GSM691137 92 DM 51 27.8 10.1 7.1 59
GSM691138 69 DM 41 31.8 8.1 5.9 51
GSM691139 63 IGT 50 26.9 6.1 5.3 77
GSM691140 88 DM 55 27.4 8.8 6.4 67
GSM69114 88 DM 32 28.8 11.7 7.0 64
GSM691142 226 DM 66 32.2 7.3 6.3 58
GSM691143 35 NGT not specified 23.6 5.5 5.5 37
GSM691144 43 DM not specified 39.1 8.5 7.3 44
GSM691145 83 IGT 54 34.2 5.7 5.3 44
GSM691146 71 IGT 37 33.1 5.6 5.7 59
GSM691147 57 NGT 55 26.4 5.1 5.5 27
GSM691148 42 DM 53 25.1 7.7 6.4 62
GSM691149 38 IGT 38 27.3 7.0 5.6 59
GSM691150 19 NGT 76 26.2 4.8 5.5 57
GSM69115 14 IGT 50 16.7 5.9 5.6 59
GSM691152 51 IGT 38 23.0 5.1 6.0 69
GSM691153 28 NGT not specified 23.1 5.1 5.4 42
GSM691154 26 NGT 69 23.2 4.9 5.3 64

Tags

  • adipocyte
  • adipose tissue
  • body
  • cell
  • glucose
  • glucose intolerance
  • line
  • obesity
  • subcutaneous adipose tissue

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