Adiponectin paper (Boursereau et al. 2017) Flashcards

1
Q

What were the authors investigating in this paper?

A

How do miRNAs relate to adiponectin’s anti-inflammatory action on skeletal muscle

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2
Q

What were the author’s objectives?

A
  • Identify any miRNAs that are regulated by adiponectin in skeletal muscle
  • Identify the functions of any identified mRNAs
  • Determine if the same miRNAs found in mice are also regulated by adiponectin in humans
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3
Q

How did the authors address which miRNAs were regulated by adiponectin in skeletal muscle?

A

miRNA arrays to identify which ones were different between muscles that were producing adiponectin vs muscles that weren’t. Then they did RT-qPCR to address how much expression was changing

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4
Q

Why did they choose to focus on miR-711?

A

It was substantially upregulated in muscle cells with adiponectin

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5
Q

What experimental evidence allowed the authors to conclude that miR-711 was a major effector of the anti-inflammatory effects of adiponectin in skeletal muscle?

A
  • miR-711 was substantially upregulated when adiponectin was being expressed, compared to the controls where the hormone wasn’t expressed
  • miR-711 is also overexpressed when adiponectin is
  • Blocking miR-711 negates any effects of adiponectin
  • Expressing only miR-711, without any adiponectin, shows the same decrease on expression the TLR4 pathway components as what it seen with adiponectin treatment alone
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6
Q

How did the authors identify the function of miR-711?

A

In silico functional analysis. They looked for sequences in the genome that were complementary to miR-711’s sequence to determine which genes may be its targets

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7
Q

Why did the authors focus on components of the TLR4 pathway when determining if miR-711 was the effector?

A

These are involved in inflammatory signalling pathways, which was the author’s topic

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8
Q

How did the authors determine if miR-711 in mice also functions as adiponectin’s effector in human skeletal muscle?

A

RT-qPCR to determine expression levels in human myotube cells that were treated in vitro with adiponectin or nothing

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