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

Tags

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

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