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Identification of a discrete subpopulation of spinal cord ependymal cells with neural stem cell properties

Stenudd, Moa (author)
Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden.
Sabelstrom, Hanna (author)
Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden.
Llorens-Bobadilla, Enric (author)
Karolinska Institutet
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Zamboni, Margherita (author)
Karolinska Institutet
Blom, Hans, 1968- (author)
KTH,Tillämpad fysik,Science for Life Laboratory, SciLifeLab
Brismar, Hjalmar (author)
Karolinska Institutet,KTH,Science for Life Laboratory, SciLifeLab,Biofysik
Zhang, Shupei (author)
Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden.
Basak, Onur (author)
Hubrecht Inst Dev Biol & Stem Cell Res, NL-3584 CT Utrecht, Netherlands.;Univ Med Ctr Utrecht, NL-3584 GC Utrecht, Netherlands.
Clevers, Hans (author)
Hubrecht Inst Dev Biol & Stem Cell Res, NL-3584 CT Utrecht, Netherlands.;Univ Med Ctr Utrecht, NL-3584 GC Utrecht, Netherlands.
Goritz, Christian (author)
Karolinska Institutet
Barnabe-Heider, Fanie (author)
Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden.;Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden.
Frisen, Jonas (author)
Karolinska Institutet
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Karolinska Institutet Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden (creator_code:org_t)
CELL PRESS, 2022
2022
English.
In: Cell Reports. - : CELL PRESS. - 2211-1247. ; 38:9
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Spinal cord ependymal cells display neural stem cell properties in vitro and generate scar-forming astrocytes and remyelinating oligodendrocytes after injury. We report that ependymal cells are functionally heterogeneous and identify a small subpopulation (8% of ependymal cells and 0.1% of all cells in a spinal cord segment), which we denote ependymal A (EpA) cells, that accounts for the in vitro stem cell potential in the adult spinal cord. After spinal cord injury, EpA cells undergo self-renewing cell division as they give rise to differentiated progeny. Single-cell transcriptome analysis revealed a loss of ependymal cell gene expression programs as EpA cells gained signaling entropy and dedifferentiated to a stem-cell-like transcriptional state after an injury. We conclude that EpA cells are highly differentiated cells that can revert to a stem cell state and constitute a therapeutic target for spinal cord repair.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

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