KASTRITI, Maria Eleni, Louis FAURE, Dorothea VON AHSEN, Thibault GERALD BOUDERLIQUE, Johan BOSTRÖM, Tatiana SOLOVIEVA, Cameron JACKSON, Marianne BRONNER, Dies MEIJER, Saida HADJAB, Francois LALLEMEND, Alek ERICKSON, Marketa KAUCKA, Viacheslav DYACHUK, Thomas PERLMANN, Laura LAHTI, Jan KŘIVÁNEK, Jean-Francois BRUNET, Kaj FRIED a Igor ADAMEYKO. Schwann cell precursors represent a neural crest-like state with biased multipotency. The Embo Journal. HOBOKEN: WILEY, 2022, roč. 41, č. 17, s. 1-28. ISSN 0261-4189. Dostupné z: https://dx.doi.org/10.15252/embj.2021108780.
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Základní údaje
Originální název Schwann cell precursors represent a neural crest-like state with biased multipotency
Autoři KASTRITI, Maria Eleni, Louis FAURE, Dorothea VON AHSEN, Thibault GERALD BOUDERLIQUE, Johan BOSTRÖM, Tatiana SOLOVIEVA, Cameron JACKSON, Marianne BRONNER, Dies MEIJER, Saida HADJAB, Francois LALLEMEND, Alek ERICKSON, Marketa KAUCKA, Viacheslav DYACHUK, Thomas PERLMANN, Laura LAHTI, Jan KŘIVÁNEK (203 Česká republika, domácí), Jean-Francois BRUNET, Kaj FRIED a Igor ADAMEYKO (garant).
Vydání The Embo Journal, HOBOKEN, WILEY, 2022, 0261-4189.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 10601 Cell biology
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 11.400
Kód RIV RIV/00216224:14110/22:00127652
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.15252/embj.2021108780
UT WoS 000822696300001
Klíčová slova anglicky Schwann cell lineage; Schwann cell precursors; multipotency; neural crest; regulons.
Štítky 14110517, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 31. 1. 2023 10:34.
Anotace
Schwann cell precursors (SCPs) are nerve-associated progenitors that can generate myelinating and non-myelinating Schwann cells but also are multipotent like the neural crest cells from which they originate. SCPs are omnipresent along outgrowing peripheral nerves throughout the body of vertebrate embryos. By using single-cell transcriptomics to generate a gene expression atlas of the entire neural crest lineage, we show that early SCPs and late migratory crest cells have similar transcriptional profiles characterised by a multipotent "hub" state containing cells biased towards traditional neural crest fates. SCPs keep diverging from the neural crest after being primed towards terminal Schwann cells and other fates, with different subtypes residing in distinct anatomical locations. Functional experiments using CRISPR-Cas9 loss-of-function further show that knockout of the common "hub" gene Sox8 causes defects in neural crest-derived cells along peripheral nerves by facilitating differentiation of SCPs towards sympathoadrenal fates. Finally, specific tumour populations found in melanoma, neurofibroma and neuroblastoma map to different stages of SCP/Schwann cell development. Overall, SCPs resemble migrating neural crest cells that maintain multipotency and become transcriptionally primed towards distinct lineages.
VytisknoutZobrazeno: 12. 5. 2024 01:38