Wnttalks: Talk by Bryjalab on Wnt5a and choroid plexus! – 6. 5. 2021

with Žádné komentáře
We cordially invite you to the Wnttalks, where our alumni Karol Kaiser, Ph.D. will present his research from Bryjalab that was focused on Wnt5 and choroid plexus in a talk:

Meis1-Wnt5a axis – The story of two choroid plexuses.

6. 5. 2021 at 11.00 and at 18.00
link to join will be published soon at: https://wnttalks.wordpress.com/


Wnttalks is a prestigious world-wide platform for online talks of Wnt researchers to present their work within Wnt community as an online version of renowned Gordon Research Conferences.
Wnttalks are rotating Europe-Australasia-America, so there is a spot for Europe only every 6 weeks. To accommodate the international nature of the community, each speaker presents twice within a 24-hour period.
We are very proud and honoured that our research topic has been nominated for the European spot!
The setup of Wnttalks is similar in philosophy to the early Wnt meetings – prioritizing trainees and early career scientists presenting their work. There will be two talks per session, each talk allotted a total of 30 minutes (20 min talk and 10 min discussion).
choroid plexus
More about the talk and the paper:

Title of the paper: MEIS-WNT5A axis regulates development of 4th ventricle choroid plexus

Karol Kaiser, Ahram Jang, Petra Kompaníková, Melody P. Lun,Jan Procházka, Ondrej Machon, Neil Dani, Michaela Procházková, Benoit Laurent, Daniel Gyllborg, Renée van Amerongen, , Ryann M. Fame, Suhasini Gupta, Feizhen Wu, Roger A. Barker, Ivana Buková, Radislav Sedláček, Zbyněk Kozmík, Ernest Arenas, Maria K. Lehtinen* and Vítězslav Bryja*


The choroid plexus (ChP) produces cerebrospinal fluid and forms a critical brain barrier. ChP tissues form in each brain ventricle, each one adopting a distinct shape, but remarkably little is known about the mechanisms underlying ChP development.  Here, we show that epithelial WNT5A is critical for determining fourth ventricle (4V)  ChP morphogenesis and size. Systemic Wnt5a knockout, or forced Wnt5a overexpression beginning at E10.5, profoundly reduced ChP size and development.

 However, Wnt5a expression was enriched in Foxj1-positive epithelial cells of 4V ChP plexus, and its conditional deletion in these cells affected the branched, villous morphology of the 4V ChP. We found that WNT5A was enriched in epithelial cells localized to the distal tips of 4V ChP villi, where WNT5A acted locally to activate noncanonical Wnt signaling via Ror1/Ror2 receptors. During 4V ChP development, MEIS1 bound to the proximal Wnt5a promoter, and gain- and loss-of-function approaches demonstrated that MEIS1 regulated Wnt5a expression. Collectively, our findings demonstrate a dual function of WNT5A in ChP development and identify MEIS transcription factors as upstream regulators of Wnt5a in the 4V ChP epithelium.

Link to the preprint of the paper: https://www.biorxiv.org/content/10.1101/2020.05.07.082370v1

Accepted in Development.