Enhancing placental function – my first publication explained

Enhancing placental function  – my first publication explained

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Four years after my Masters of Research in Maternal and Fetal Health at The University of Manchester, our paper is finally published in Theranostics which means I have my first science journal publication! As other scientists will know, this is a very exciting moment in our science journey.

 

The title is “Placental Homing Peptide-microRNA Inhibitor Conjugates for Targeted Enhancement of Intrinsic Placental Growth Signaling”. What does that mean?! In simple terms, it’s all about targeting the placenta in order to enhance its function by delivering therapeutic molecules to it. Science journals can be very inaccessible to non-scientists but it is so important we relay our scientific findings to the public. I’m going to talk about why an earth we did this research, how we did it, our results and what they mean… and hopefully it all makes sense and you’ve learnt something new!

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The background…

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Many serious pregnancy complications such as pre-eclampsia (high blood pressure and protein present in the urine), fetal growth restriction (FGR; baby is smaller than average) and macrosomia (baby is larger than average) develop as a result of suboptimal growth and development of the placenta. The placenta is the interface between mother and baby for nutrient transfer.

These conditions can lead to preterm delivery which in turn can cause complications. Babies who are born too early have an increased risk of developing cardiovascular and metabolic diseases, but there are currently no treatments available during pregnancy. Administration of a drug via an injection in human pregnancy can cause dangerous side effects and disturbances to the fetus’ development (teratogenicity). We all take pain killers for headaches from time-to-time right? You just pop them into your mouth, and the drug circulates throughout your whole body. This means at the site of pain, the drug is more diluted but may also result in unwanted effects.

This paper is therefore all about trying to target the placenta specifically with a therapeutic to improve placental growth and development. The human placenta has two different layers: the outer syncytium, which is the site of nutrient transfer, and the underlying layer of proliferating cytotrophoblasts (CTB). These CTBs are important for growth and supporting nutritional demands of the growing fetus. These cells divide, and fuse with the syncytium.

  • Low proliferation of CTB = FGR and pre-eclampsia
  • High proliferation of CTB = macrosomia

The rate of growth/proliferation is affected by various hormones and growth factors, but also regulated by small RNA molecules called microRNAs (miRs). These regulate gene expression and consequently alter various biological processes such as cell proliferation. miR-145 and miR-675 are known to cause a reduction in placental growth, and so inhibiting these could improve placental growth in the pregnant women. But how does this get around the issue of teratogenicity? Well, our group have shown it’s possible to deliver a therapeutic molecule, which is packaged in lipids (a liposome), specifically to the placenta with minimising unwanted effects in the mother and fetus. This is done by using a specific placental homing peptide conjugate (a link of small molecules that form the foundations of proteins) which selectively binds to the placental surface. Think of it as a molecular postcode for the placenta!

structure miR inhibitor

So, put two and two together and in this paper we tried to use placental homing peptides to deliver miR-145 and miR-675 inhibitors directly to the placenta with the aim to enhance placental growth.

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What did we do?

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Testing the safety of miR inhibitor delivery

Ensuring that the miR inhibitors can be used as a clinical intervention for poor placental growth and development means prior safety testing. We need to make sure that their delivery doesn’t cause detrimental effects. We exposed pregnant mice to either a short or longer-term treatment of a fluorescent-labelled non-specific inhibitor. With a fluorescence microscope we visualised the presence and localisation of it (miR inhibitor in green) within the mouse placenta. Localisation of the miR inhibitor was found in the short-term treatment and also in the longer term one too.Results2 - fluor distribution writing

The miR inhibitor was not found in fetal tissues which is great! However, we found it localised in some of the maternal tissues suggesting a possibility of off-target effects – something that would need to be investigated further. The non-specific miR inhibitor didn’t cause a change to fetal or placental weight, litter size or the present of fetal abnormalities, so this indicates that it’s tolerated well in pregnancy… phew!

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Testing specific miR inhibitors in mice

Pregnant mice were either injected with a control solution (PBS), the non-specific (scrambled) inhibitor, or the treatments miR-675 inhibitor or miR-145 inhibitor.

Placental weight:

The miR-675 inhibitor did significantly increase placental weight. However, miR-145 did not. Despite this, interestingly a statistical test confirmed that it did reduce variability in placental weight. No placentas fell below the 10th weight centile for either inhibitor, which suggests they have growth-promoting effects.

Fetal weight:

Both miR-675 and miR-145 inhibitors increased fetal weight but the non-specific inhibitor altered the fetal weight distribution as well. At the moment, we aren’t too sure why. One potential reason could be species-specific effects, but if you want to geek out, check out the discussion section of the paper (link below) where other suggestions are discussed!

Results4 - placetnal fetal weight writing

We also tested the two specific miR inhibitors for any changes in litter size and number of miscarriages. Neither had an effect therefore further suggesting that this novel treatment is safe to use in pregnant mice, another step in the right direction!

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Testing the specific inhibitors in human tissue

Placental explants, which are chunks of fresh tissue, from first trimester (early pregnancy) and term (end of pregnancy) were cultured in the miR-675 inhibitor or miR-145 inhibitor with or without the placental homing peptide added on.  Both miR-675 and miR-145 with the peptide significantly increased the placental CTB cell proliferation, but so did their equivalents without the homing peptide, which was interesting. This enhanced cell proliferation was only found in first trimester placental samples.

Results5 - human prolif writing

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Summary

Without getting bogged down in all the intense sciencey discussion of this data (again, feel free to view the link for the actual paper below if you would like to read some more), what can we conclude from this study?

  • We provide evidence that the use of these homing peptides have a favourable therapeutic profile during pregnancy – they appear safe to use!
  • It’s the first piece of evidence for targeted delivery of a miR inhibitor to the placenta.
  • A homing peptide-miRNA inhibitor can be used to increase human placental growth in early pregnancy, which means it should be possible to manipulate the expression of those pesky placental miRs which contribute to pre-eclampsia and FGR.
  • This study suggests that these novel therapeutics may provide a new strategy for targeted treatment of compromised placental development and function.

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Of course further research is required to push the therapeutic potential of placental homing peptide-microRNA inhibitors further in the hope they will enter clinical trials in the future, but this study provides some really interesting data. Watch this space!

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You can find the original paper here!

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This was a much more science-heavy blog post than I normally write. Would you like more science explained posts?

Please comment below as always to let me know what you thought. Your feedback really is valuable to me. It helps me to grow as a science blogger and get the information out there that you like to read!

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2 thoughts on “Enhancing placental function – my first publication explained

  1. This was very well written! Your breakdown of the paper was effective in telling the story of your work. It’s always fun to read about what other researchers are working on in different fields from your own.

    Like

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