Single-cell multi-omic atlas and morphogen screening informs midbrain and hindbrain organoid engineering

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Authors: Nadezhda Azbukina, Zhisong He, Hsiu‐Chuan Lin, Małgorzata Santel, Bijan Kashanian, Ashley Maynard, Tivadar Török, Ryoko Okamoto, Marina T. Nikolova, Makiko Seimiya, Sabina Kanton, Valentin Brösamle
+3 more René Holtackers, J. Gray Camp, Barbara Treutlein
Cited by: 1
References: 98

Abstract

Patterning of the neural tube establishes midbrain and hindbrain structures that coordinate motor movement, process sensory input and integrate cognitive functions. Cellular impairment within these structures underlies diverse neurological disorders, and in vitro organoid models promise inroads to understanding development and modeling disease. Here, we use paired single-cell transcriptome and accessible chromatin sequencing to map cell composition and regulatory mechanisms in organoid models of midbrain and hindbrain. We find that existing midbrain organoid protocols generate ventral and dorsal cell types, covering regions including floor plate, dorsal and ventral midbrain and adjacent hindbrain regions. Gene regulatory network inference and transcription factor perturbation resolve mechanisms underlying neuronal differentiation. A single-cell multiplexed patterning screen identifies morphogen concentrations that expand existing organoid models, including conditions generating medulla glycinergic neurons and cerebellum glutamatergic subtypes. Together, the multi-omic atlas and morphogen screen reveal morphogen-regulon relationships guiding region-specific progenitor differentiation towards diverse neuron types of the posterior brain.

Fields of Study & Subjects

Single-cell and spatial transcriptomics Neurogenesis and neuroplasticity mechanisms Pluripotent Stem Cells Research

Publication details

Journal / source
Nature Neuroscience
Publisher
Springer Science and Business Media LLC
Volume
29
Issue
7
Pages
1548–1558
Publication date
3 June 2026
Language
EN