Niche stiffness underlies the ageing of central nervous system progenitor cells.
Adult Stem Cells
/ pathology
Aging
/ pathology
Animals
Animals, Newborn
Cell Count
Central Nervous System
/ pathology
Extracellular Matrix
/ pathology
Female
Humans
Membrane Proteins
/ antagonists & inhibitors
Multipotent Stem Cells
/ pathology
Oligodendroglia
/ pathology
Rats
Stem Cell Niche
/ physiology
Journal
Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
07
04
2017
accepted:
15
07
2019
pubmed:
16
8
2019
medline:
31
3
2020
entrez:
16
8
2019
Statut:
ppublish
Résumé
Ageing causes a decline in tissue regeneration owing to a loss of function of adult stem cell and progenitor cell populations
Identifiants
pubmed: 31413369
doi: 10.1038/s41586-019-1484-9
pii: 10.1038/s41586-019-1484-9
pmc: PMC7025879
mid: EMS83737
doi:
Substances chimiques
Membrane Proteins
0
Piezo1 protein, rat
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
130-134Subventions
Organisme : Medical Research Council
ID : MR/M011089/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_12009
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/K017047/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/N006402/1
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UP_1002/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 203151
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R015635/1
Pays : United Kingdom
Commentaires et corrections
Type : ErratumIn
Références
Goodell, M. A. & Rando, T. A. Stem cells and healthy aging. Science 350, 1199–1204 (2015).
doi: 10.1126/science.aab3388
Sim, F. J., Zhao, C., Penderis, J. & Franklin, R. J. M. The age-related decrease in CNS remyelination efficiency is attributable to an impairment of both oligodendrocyte progenitor recruitment and differentiation. J. Neurosci. 22, 2451–2459 (2002).
doi: 10.1523/JNEUROSCI.22-07-02451.2002
Gopinath, S. D. & Rando, T. A. Stem cell review series: aging of the skeletal muscle stem cell niche. Aging Cell 7, 590–598 (2008).
doi: 10.1111/j.1474-9726.2008.00399.x
Swift, J. et al. Nuclear lamin-A scales with tissue stiffness and enhances matrix-directed differentiation. Science 341, 1240104 (2013).
doi: 10.1126/science.1240104
Hinks, G. L. & Franklin, R. J. Delayed changes in growth factor gene expression during slow remyelination in the CNS of aged rats. Mol. Cell. Neurosci. 16, 542–556 (2000).
doi: 10.1006/mcne.2000.0897
Tang, D. G., Tokumoto, Y. M., Apperly, J. A., Lloyd, A. C. & Raff, M. C. Lack of replicative senescence in cultured rat oligodendrocyte precursor cells. Science 291, 868–871 (2001).
doi: 10.1126/science.1056780
Keough, M. B. et al. An inhibitor of chondroitin sulfate proteoglycan synthesis promotes central nervous system remyelination. Nat. Commun. 7, 11312 (2016).
doi: 10.1038/ncomms11312
He, L., Si, G., Huang, J., Samuel, A. D. T. & Perrimon, N. Mechanical regulation of stem-cell differentiation by the stretch-activated Piezo channel. Nature 555, 103–106 (2018).
doi: 10.1038/nature25744
Eisenhoffer, G. T. et al. Crowding induces live cell extrusion to maintain homeostatic cell numbers in epithelia. Nature 484, 546–549 (2012).
doi: 10.1038/nature10999
Li, J. et al. Piezo1 integration of vascular architecture with physiological force. Nature 515, 279–282 (2014).
doi: 10.1038/nature13701
McHugh, B. J. et al. Integrin activation by Fam38A uses a novel mechanism of R-Ras targeting to the endoplasmic reticulum. J. Cell Sci. 123, 51–61 (2010).
doi: 10.1242/jcs.056424
McHugh, B. J., Murdoch, A., Haslett, C. & Sethi, T. Loss of the integrin-activating transmembrane protein Fam38A (Piezo1) promotes a switch to a reduced integrin-dependent mode of cell migration. PLoS One 7, e40346 (2012).
doi: 10.1371/journal.pone.0040346
Jäkel, S. et al. Altered human oligodendrocyte heterogeneity in multiple sclerosis. Nature 566, 543–547 (2019).
doi: 10.1038/s41586-019-0903-2
Suzuki, K. et al. In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration. Nature 540, 144–149 (2016).
doi: 10.1038/nature20565
Nissim, L., Perli, S. D., Fridkin, A., Perez-Pinera, P. & Lu, T. K. Multiplexed and programmable regulation of gene networks with an integrated RNA and CRISPR/Cas toolkit in human cells. Mol. Cell 54, 698–710 (2014).
doi: 10.1016/j.molcel.2014.04.022
Chan, K. Y. et al. Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems. Nat. Neurosci. 20, 1172–1179 (2017).
doi: 10.1038/nn.4593
Duncan, I. D., Brower, A., Kondo, Y., Curlee, J. F. Jr & Schultz, R. D. Extensive remyelination of the CNS leads to functional recovery. Proc. Natl Acad. Sci. USA 106, 6832–6836 (2009); correction 106, 12208 (2009).
doi: 10.1073/pnas.0812500106
Sellers, D. L., Maris, D. O. & Horner, P. J. Postinjury niches induce temporal shifts in progenitor fates to direct lesion repair after spinal cord injury. J. Neurosci. 29, 6722–6733 (2009).
doi: 10.1523/JNEUROSCI.4538-08.2009
Koser, D. E., Moeendarbary, E., Hanne, J., Kuerten, S. & Franze, K. CNS cell distribution and axon orientation determine local spinal cord mechanical properties. Biophys. J. 108, 2137–2147 (2015).
doi: 10.1016/j.bpj.2015.03.039
Christ, A. F. et al. Mechanical difference between white and gray matter in the rat cerebellum measured by scanning force microscopy. J. Biomech. 43, 2986–2992 (2010).
doi: 10.1016/j.jbiomech.2010.07.002
Franze, K. et al. Spatial mapping of the mechanical properties of the living retina using scanning force microscopy. Soft Matter 7, 3147–3154 (2011).
doi: 10.1039/c0sm01017k
Hertz, H. Über die Berührung fester elastischer Körper. J. Reine Angew. Math. 92, 156–171 (1881).
Koser, D. E. et al. Mechanosensing is critical for axon growth in the developing brain. Nat. Neurosci. 19, 1592–1598 (2016).
doi: 10.1038/nn.4394
Moshayedi, P. et al. Mechanosensitivity of astrocytes on optimized polyacrylamide gels analyzed by quantitative morphometry. J. Phys. Condens. Matter 22, 194114 (2010).
doi: 10.1088/0953-8984/22/19/194114
Boudou, T. et al. An extended modeling of the micropipette aspiration experiment for the characterization of the Young’s modulus and Poisson’s ratio of adherent thin biological samples: numerical and experimental studies. J. Biomech. 39, 1677–1685 (2006).
doi: 10.1016/j.jbiomech.2005.04.026
Khazipov, R. et al. Atlas of the postnatal rat brain in stereotaxic coordinates. Front. Neuroanat. 9, 161 (2015).
doi: 10.3389/fnana.2015.00161
Woodruff, R. H. & Franklin, R. J. M. Demyelination and remyelination of the caudal cerebellar peduncle of adult rats following stereotaxic injections of lysolecithin, ethidium bromide, and complement/anti-galactocerebroside: a comparative study. Glia 25, 216–228 (1999).
doi: 10.1002/(SICI)1098-1136(19990201)25:3<216::AID-GLIA2>3.0.CO;2-L
Jeffery, N. D. & Blakemore, W. F. Remyelination of mouse spinal cord axons demyelinated by local injection of lysolecithin. J. Neurocytol. 24, 775–781 (1995).
doi: 10.1007/BF01191213
De Waele, J. et al. 3D culture of murine neural stem cells on decellularized mouse brain sections. Biomaterials 41, 122–131 (2015).
doi: 10.1016/j.biomaterials.2014.11.025
Kay, M. A., He, C.-Y. & Chen, Z.-Y. A robust system for production of minicircle DNA vectors. Nat. Biotechnol. 28, 1287–1289 (2010).
doi: 10.1038/nbt.1708
Challis, R. C. et al. Widespread and targeted gene expression by systemic AAV vectors: production, purification, and administration. Preprint at https://doi.org/10.1101/246405 (2018).
Pertea, M., Kim, D., Pertea, G. M., Leek, J. T. & Salzberg, S. L. Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie and Ballgown. Nature Protocols 11, 1650–1667 (2016).
doi: 10.1038/nprot.2016.095