I'm thrilled to share our latest published paper in @eLife
where we applied cryo-EM to brain organoids to look at ultrastructure of human axons with unprecedented resolution!
Check out the lovely cryo-CLEM clip below.
And a short 🧵 of what we found.
First off, we established a method to culture our air-liquid interface organoid cultures with EM grids to get outgrowth of axon bundles onto the grids. This enables capture of "clean" axons without dendrites like you normally get with cells in vitro.
Then, using correlative light and electron microscopy (CLEM) we could trace axon bundles and focus in on GFP labeled axons within bundles to explore their intracellular architecture.
We found that human growing axons are really unique! For example we know that microtubules are parallel and unidirectional in axons, and we could see that, but we even had the resolution to do subtomogram averaging and see individual protofilaments.
We also found some really interesting ER morphologies that seem to be unique to axons, with incredibly thin tubules almost completely lacking lumen, pointing to a primary role in lipid biosynthesis in this context, which makes sense given the huge surface area of axons.
Finally, we were surprised by the scarcity of ribosomes specifically in the axon shaft, a finding previously seen in more traditional EM, but now corroborated with cryo-EM which has the resolution to pick up even monosomes if they are there.
This has implications in terms of protein biogenesis, and suggests that local translation is not a major contributor along the length of the axon. Importantly, other neuronal processes (i.e. dendrites) had plenty of ribosomes, and we did not capture synapses or growth cones.
We hope that this big dataset of tomograms from human axons will be a useful resource for the community. Explore for yourself and access the full dataset on EMDB and EMPIAR (accession codes in the paper).
This was an awesome collaboration between my lab and @KukulskiWanda. It was the serendipitous result of our labs being next door, and many fruitful lunch breaks with co-first authors Patrick Hoffmann and Stefano Giandomenico. It helps to have friends that can do amazing science!!
• • •
Missing some Tweet in this thread? You can try to
force a refresh
📢New Lancaster Lab paper out now! Check it out, we've discovered a cool way evolution has played with cell shape to make our brains BIG! 🧵 cell.com/cell/fulltext/…
This is a question I've been interested in since starting my lab 6 years ago. And so this paper is a really big deal for me and the lab! So where to start...
We know that the human brain is about 3 times bigger than chimps' and gorillas' but why? How?
We can't (nor would we want to) do experiments on developing ape brains, so we approached this question by using brain organoids, little pea-sized replicas of early brain tissue. And when we made organoids from different apes, there was a clear difference in size!
New preprint from the lab. We’ve joined the fight, and looked at tropism of the virus causing #COVID19 in the brain. Great collaboration with @AnnaAlbecka and Leo James group. Here’s a breakdown of what we find. 🧵
We first look at expression of the viral receptors in human brain organoids and find not much expression, at least at the RNA level, in neural cells. BUT interestingly we find a lot of expression in the choroid plexus. So... what’s the choroid plexus you say?
The choroid plexus (ChP) is what makes your cerebrospinal fluid! It’s also a really important barrier that prevents things from entering the CSF from the blood. So it’s like a gatekeeper, protecting the brain from viruses, toxic compounds and immune cells and factors.