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10.1016/j.stem.2016.07.004

http://scihub22266oqcxt.onion/10.1016/j.stem.2016.07.004
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suck abstract from ncbi


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pmid27524439
      Cell+Stem+Cell 2016 ; 19 (4 ): 530-543
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  • Proximity-Based Differential Single-Cell Analysis of the Niche to Identify Stem/Progenitor Cell Regulators #MMPMID27524439
  • Silberstein L ; Goncalves KA ; Kharchenko PV ; Turcotte R ; Kfoury Y ; Mercier F ; Baryawno N ; Severe N ; Bachand J ; Spencer JA ; Papazian A ; Lee D ; Chitteti BR ; Srour EF ; Hoggatt J ; Tate T ; Lo Celso C ; Ono N ; Nutt S ; Heino J ; Sipilä K ; Shioda T ; Osawa M ; Lin CP ; Hu GF ; Scadden DT
  • Cell Stem Cell 2016[Oct]; 19 (4 ): 530-543 PMID27524439 show ga
  • Physiological stem cell function is regulated by secreted factors produced by niche cells. In this study, we describe an unbiased approach based on the differential single-cell gene expression analysis of mesenchymal osteolineage cells close to, and further removed from, hematopoietic stem/progenitor cells (HSPCs) to identify candidate niche factors. Mesenchymal cells displayed distinct molecular profiles based on their relative location. We functionally examined, among the genes that were preferentially expressed in proximal cells, three secreted or cell-surface molecules not previously connected to HSPC biology-the secreted RNase angiogenin, the cytokine IL18, and the adhesion molecule Embigin-and discovered that all of these factors are HSPC quiescence regulators. Therefore, our proximity-based differential single-cell approach reveals molecular heterogeneity within niche cells and can be used to identify novel extrinsic stem/progenitor cell regulators. Similar approaches could also be applied to other stem cell/niche pairs to advance the understanding of microenvironmental regulation of stem cell function.
  • |*Stem Cell Niche [MESH]
  • |Animals [MESH]
  • |Bone Marrow Cells/cytology [MESH]
  • |Bone and Bones/cytology [MESH]
  • |Cell Lineage/genetics [MESH]
  • |Cell Self Renewal/genetics [MESH]
  • |Cell Separation [MESH]
  • |Gene Deletion [MESH]
  • |Gene Expression Profiling [MESH]
  • |Hematopoietic Stem Cells/*cytology/metabolism [MESH]
  • |Interleukin-18/metabolism [MESH]
  • |Membrane Glycoproteins/metabolism [MESH]
  • |Ribonuclease, Pancreatic/metabolism [MESH]
  • |Single-Cell Analysis/*methods [MESH]
  • |Time Factors [MESH]
  • |Transcription, Genetic [MESH]


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  • suck abstract from ncbi

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