basic & translational research on CSF-based signaling & choroid plexus • find us @HMS_Neuro & @BostonChildrens Pathology Dept • // account run by lab members
🌟 Review led by @ScienceYael on apocrine secretion at the choroid plexus: evidence across imaging/proteomics🔬, regulatory cues, and CSF proteome impact
New from our lab: in mice, maternal psychedelics reach embryonic CSF within minutes, activate the choroid plexus, and alter development with adult behavior effects. Thread🧵👇
🚨 Psychedelics in pregnancy - can a single dose reach the embryo and matter? Yes. In mice they hit embryonic CSF within minutes, activate choroid plexus→CSF axis, & shift cortical development w adult behavioral signatures. @LehtinenLab Preprint:
biorxiv.org/content/10.1101/…
1/13
We uncovered a new serotonergic axis — from the ChP to the CSF — that sculpts the developing brain. It’s powerful, fast, and vulnerable to disruption. This work opens a new window into how 🤰 influence lifelong brain function. 📖 Full paper: rdcu.be/eoaSY
Maternal exposure to the psychedelic LSD triggered the same ChP secretory response. Within 30 minutes, nearly 70% of embryonic ChP cells formed aposomes.
This suggests serotonergic drugs in pregnancy may directly alter brain development via the CSF.
These brain changes translated into long-term behavioral effects.
Mice exposed in utero to repeated ChP activation showed:
⬇ Less social interaction
⬇Fewer repetitive behaviors
– Altered courtship vocalizations
Neurodevelopmental outcomes, shifted before birth.
Apocrine secretion didn’t just reshape the cortex, it altered proliferation in the lateral ganglionic eminence (LGE) too. We saw shifts in interneurons, glia, and microglia.
This pathway impacts multiple brain regions and cell types during development.
When we triggered ChP secretion during neurogenesis, the consequences were striking.
We saw shifts in neuronal fate:
⬆ SATB2+ callosal projection neurons
⬇ TBR1+ corticothalamic neurons
These changes were layer-specific — reorganizing cortical architecture at its foundation.
Apocrine secretion changes the composition of the CSF in minutes. We found a surge of key developmental signals including IGF2, Sonic Hedgehog (SHH), insulin, & transthyretin (TTR). Each of these proteins is known to shape how neural progenitors divide and differentiate.
So what sets off this secretory burst? Among other things, activation of the serotonin receptor 5-HT2C. We showed that stimulating 5-HT2C triggers a wave of calcium signaling followed by apocrine secretion in the embryonic ChP, flooding the CSF w key developmental signals.
Balloon-like structures, called aposomes, form at the surface of ChP cells & release huge amounts of protein directly into the CSF. This is a high-volume, coordinated secretion mechanism, & it massively expands our understanding of how the ChP contributes to brain development.
We discovered the choroid plexus (ChP) doesn’t just secrete tiny vesicles & exosomes. It also unleashes large apocrine secretory structures packed with proteins that flood cerebrospinal fluid (CSF) during brain development. This changes how we think about embryonic 🧠 signaling.
Led by @ScienceYael and out today in @NatureNeuro: the brain's fluid-secreting organ — the choroid plexus — can reshape neural development through a powerful, little-known process. & it can be hijacked by serotonergic drugs like LSD. 🧠👇 A thread rdcu.be/eoaSY
So so so honored to be featured in @SfNtweets Newsletter as part of the Future of Neuroscience! If you want to know a little more about my background, PhD work, and future goals, this one’s for you! :)
sfn.org/publications/neurosc…