Abstract

A better understanding of the cell-fate transitions that occur in complex cellular ecosystems in normal development and disease could inform cell engineering efforts and lead to improved therapies. However, a major challenge is to simultaneously identify new cell states, and their transitions, to elucidate the gene expression dynamics governing cell-type diversification. Here, we present CellRouter, a multifaceted single-cell analysis platform that identifies complex cell-state transition trajectories by using flow networks to explore the subpopulation structure of multi-dimensional, single-cell omics data. We demonstrate its versatility by applying CellRouter to single-cell RNA sequencing data sets to reconstruct cell-state transition trajectories during hematopoietic stem and progenitor cell (HSPC) differentiation to the erythroid, myeloid and lymphoid lineages, as well as during re-specification of cell identity by cellular reprogramming of monocytes and B-cells to HSPCs. CellRouter opens previously undescribed paths for in-depth characterization of complex cellular ecosystems and establishment of enhanced cell engineering approaches.

Details

Title
Reconstruction of complex single-cell trajectories using CellRouter
Author
Edroaldo Lummertz da Rocha 1   VIAFID ORCID Logo  ; R Grant Rowe 1 ; Lundin, Vanessa 1 ; Mohan Malleshaiah 2 ; Jha, Deepak Kumar 1 ; Rambo, Carlos R 3 ; Hu, Li 4   VIAFID ORCID Logo  ; North, Trista E 5 ; Collins, James J 6 ; Daley, George Q 1 

 Stem Cell Transplantation Program, Division of Pediatric Hematology and Oncology, Boston Children’s Hospital and Dana-Farber Cancer Institute, Boston, MA, USA; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA; Harvard Stem Cell Institute, Cambridge, MA, USA; Manton Center for Orphan Disease Research, Boston, MA, USA 
 Department of Systems Biology, Harvard Medical School, Boston, MA, USA; Division of Systems Biology, Montreal Clinical Research Institute, 110 Avenue Des Pins Ouest, Montreal, QC H2W, Canada 
 Department of Electrical and Electronic Engineering, Federal University of Santa Catarina, Florianopolis, Brazil 
 Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, USA 
 Stem Cell Transplantation Program, Division of Pediatric Hematology and Oncology, Boston Children’s Hospital and Dana-Farber Cancer Institute, Boston, MA, USA; Harvard Stem Cell Institute, Cambridge, MA, USA 
 Institute for Medical Engineering & Science, Department of Biological Engineering, and Synthetic Biology Center, Massachusetts Institute of Technology, Broad Institute of MIT and Harvard, Cambridge, MA, USA; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA 
Pages
1-13
Publication year
2018
Publication date
Mar 2018
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2009579454
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.