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Merck
  • Multiple origins and modularity in the spatiotemporal emergence of cerebellar astrocyte heterogeneity.

Multiple origins and modularity in the spatiotemporal emergence of cerebellar astrocyte heterogeneity.

PLoS biology (2018-09-28)
Valentina Cerrato, Elena Parmigiani, María Figueres-Oñate, Marion Betizeau, Jessica Aprato, Ishira Nanavaty, Paola Berchialla, Federico Luzzati, Claudio de'Sperati, Laura López-Mascaraque, Annalisa Buffo
摘要

The morphological, molecular, and functional heterogeneity of astrocytes is under intense scrutiny, but how this diversity is ontogenetically achieved remains largely unknown. Here, by quantitative in vivo clonal analyses and proliferation studies, we demonstrate that the major cerebellar astrocyte types emerge according to an unprecedented and remarkably orderly developmental program comprising (i) a time-dependent decline in both clone size and progenitor multipotency, associated with clone allocation first to the hemispheres and then to the vermis(ii) distinctive clonal relationships among astrocyte types, revealing diverse lineage potentials of embryonic and postnatal progenitors; and (iii) stereotyped clone architectures and recurrent modularities that correlate to layer-specific dynamics of postnatal proliferation/differentiation. In silico simulations indicate that the sole presence of a unique multipotent progenitor at the source of the whole astrogliogenic program is unlikely and rather suggest the involvement of additional committed components.

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Sigma-Aldrich
抗NeuN抗体,克隆A60, clone A60, Chemicon®, from mouse
Sigma-Aldrich
Triton X-100, laboratory grade
Sigma-Aldrich
抗 AQP4 兔抗, affinity isolated antibody, Prestige Antibodies® Powered by Atlas Antibodies, buffered aqueous glycerol solution
Sigma-Aldrich
2-苯基吲哚, technical grade, 95%
Sigma-Aldrich
抗脑脂质结合蛋白抗体, from rabbit, purified by affinity chromatography