Single-Cell Profiling Reveals Sex, Lineage, and Regional Diversity in the Mouse Kidney

Chronic kidney disease affects 10% of the population with notable differences in ethnic and sex-related susceptibility to kidney injury and disease. Kidney dysfunction leads to significant morbidity and mortality and chronic disease in other organ systems. A mouse-organ-centered understanding underl...

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Published inDevelopmental cell Vol. 51; no. 3; pp. 399 - 413.e7
Main Authors Ransick, Andrew, Lindström, Nils O., Liu, Jing, Zhu, Qin, Guo, Jin-Jin, Alvarado, Gregory F., Kim, Albert D., Black, Hannah G., Kim, Junhyong, McMahon, Andrew P.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 04.11.2019
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Abstract Chronic kidney disease affects 10% of the population with notable differences in ethnic and sex-related susceptibility to kidney injury and disease. Kidney dysfunction leads to significant morbidity and mortality and chronic disease in other organ systems. A mouse-organ-centered understanding underlies rapid progress in human disease modeling and cellular approaches to repair damaged systems. To enhance an understanding of the mammalian kidney, we combined anatomy-guided single-cell RNA sequencing of the adult male and female mouse kidney with in situ expression studies and cell lineage tracing. These studies reveal cell diversity and marked sex differences, distinct organization and cell composition of nephrons dependent on the time of nephron specification, and lineage convergence, in which contiguous functionally related cell types are specified from nephron and collecting system progenitor populations. A searchable database, Kidney Cell Explorer (https://cello.shinyapps.io/kidneycellexplorer/), enables gene-cell relationships to be viewed in the anatomical framework of the kidney. [Display omitted] •Proximal nephron segments show distinct expression profiles between the sexes•The time of nephron formation determines position and segmental cell diversity•Lineage convergence is observed at nephron-collecting system junctions•Data can be queried and viewed within an annotated anatomical database Ransick et al. combined in-depth single-cell profiling of male and female adult kidneys with cluster registration to kidney structures to generate an anatomical atlas of the mammalian nephron and collecting system. Kidney Cell Explorer (https://cello.shinyapps.io/kidneycellexplorer/) enables gene-cell relationships to be viewed in the anatomical framework of the mammalian kidney.
AbstractList Chronic kidney disease affects 10% of the population with notable differences in ethnic and sex-related susceptibility to kidney injury and disease. Kidney dysfunction leads to significant morbidity and mortality and chronic disease in other organ systems. A mouse-organ-centered understanding underlies rapid progress in human disease modeling and cellular approaches to repair damaged systems. To enhance an understanding of the mammalian kidney, we combined anatomy-guided single-cell RNA sequencing of the adult male and female mouse kidney with in situ expression studies and cell lineage tracing. These studies reveal cell diversity and marked sex differences, distinct organization and cell composition of nephrons dependent on the time of nephron specification, and lineage convergence, in which contiguous functionally related cell types are specified from nephron and collecting system progenitor populations. A searchable database, Kidney Cell Explorer (https://cello.shinyapps.io/kidneycellexplorer/), enables gene-cell relationships to be viewed in the anatomical framework of the kidney.
Chronic kidney disease affects 10% of the population with notable differences in ethnic and sex-related susceptibility to kidney injury and disease. Kidney dysfunction leads to significant morbidity and mortality and chronic disease in other organ systems. A mouse-organ-centered understanding underlies rapid progress in human disease modeling and cellular approaches to repair damaged systems. To enhance an understanding of the mammalian kidney, we combined anatomy-guided single-cell RNA sequencing of the adult male and female mouse kidney with in situ expression studies and cell lineage tracing. These studies reveal cell diversity and marked sex differences, distinct organization and cell composition of nephrons dependent on the time of nephron specification, and lineage convergence, in which contiguous functionally related cell types are specified from nephron and collecting system progenitor populations. A searchable database, Kidney Cell Explorer (https://cello.shinyapps.io/kidneycellexplorer/), enables gene-cell relationships to be viewed in the anatomical framework of the kidney.Chronic kidney disease affects 10% of the population with notable differences in ethnic and sex-related susceptibility to kidney injury and disease. Kidney dysfunction leads to significant morbidity and mortality and chronic disease in other organ systems. A mouse-organ-centered understanding underlies rapid progress in human disease modeling and cellular approaches to repair damaged systems. To enhance an understanding of the mammalian kidney, we combined anatomy-guided single-cell RNA sequencing of the adult male and female mouse kidney with in situ expression studies and cell lineage tracing. These studies reveal cell diversity and marked sex differences, distinct organization and cell composition of nephrons dependent on the time of nephron specification, and lineage convergence, in which contiguous functionally related cell types are specified from nephron and collecting system progenitor populations. A searchable database, Kidney Cell Explorer (https://cello.shinyapps.io/kidneycellexplorer/), enables gene-cell relationships to be viewed in the anatomical framework of the kidney.
Chronic kidney disease affects 10% of the population with notable differences in ethnic and sex-related susceptibility to kidney injury and disease. Kidney dysfunction leads to significant morbidity and mortality and chronic disease in other organ systems. A mouse-organ-centered understanding underlies rapid progress in human disease modeling and cellular approaches to repair damaged systems. To enhance an understanding of the mammalian kidney, we combined anatomy-guided single-cell RNA sequencing of the adult male and female mouse kidney with in situ expression studies and cell lineage tracing. These studies reveal cell diversity and marked sex differences, distinct organization and cell composition of nephrons dependent on the time of nephron specification, and lineage convergence, in which contiguous functionally related cell types are specified from nephron and collecting system progenitor populations. A searchable database, Kidney Cell Explorer (https://cello.shinyapps.io/kidneycellexplorer/), enables gene-cell relationships to be viewed in the anatomical framework of the kidney. [Display omitted] •Proximal nephron segments show distinct expression profiles between the sexes•The time of nephron formation determines position and segmental cell diversity•Lineage convergence is observed at nephron-collecting system junctions•Data can be queried and viewed within an annotated anatomical database Ransick et al. combined in-depth single-cell profiling of male and female adult kidneys with cluster registration to kidney structures to generate an anatomical atlas of the mammalian nephron and collecting system. Kidney Cell Explorer (https://cello.shinyapps.io/kidneycellexplorer/) enables gene-cell relationships to be viewed in the anatomical framework of the mammalian kidney.
Chronic kidney disease affects 10% of the population with notable differences in ethnic and sex-related susceptibility to kidney injury and disease. Kidney dysfunction leads to significant morbidity and mortality, and chronic disease in other organ systems. A mouse organ-centered understanding underlies rapid progress in human disease modeling and cellular approaches to repair damaged systems. To enhance an understanding of the mammalian kidney, we combined anatomy-guided single cell RNA sequencing of the adult male and female mouse kidney with in situ expression studies and cell lineage tracing. These studies reveal cell diversity and marked sex differences, distinct organization and cell composition of nephrons dependent on the time of nephron specification, and lineage convergence, in which contiguous functionally-related cell types are specified from nephron and collecting system progenitor populations. A searchable database, Kidney Cell Explorer ( https://cello.shinyapps.io/kidneycellexplorer/ ), enables gene-cell relationships to be viewed in the anatomical framework of the kidney. Ransick et al. combined in depth single cell profiling of male and female adult kidneys with cluster registration to kidney structures to generate an anatomical atlas of the mammalian nephron and collecting system. Kidney Cell Explorer (( https://cello.shinyapps.io/kidneycellexplorer/ ) enables gene-cell relationships to be viewed in the anatomical framework of the mammalian kidney.
Author Lindström, Nils O.
Ransick, Andrew
Kim, Junhyong
Liu, Jing
Guo, Jin-Jin
Alvarado, Gregory F.
Kim, Albert D.
Black, Hannah G.
Zhu, Qin
McMahon, Andrew P.
AuthorAffiliation 3 Department of Biology, University of Pennsylvania, 415 S. University Ave, Philadelphia, PA 19104, USA
1 Department of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90089, USA
2 Graduate Program in Genomics and Computational Biology, Biomedical Graduate Studies, University of Pennsylvania, 160 BRB II/III - 421 Curie Blvd, Philadelphia, PA, 19104-6064, USA
AuthorAffiliation_xml – name: 2 Graduate Program in Genomics and Computational Biology, Biomedical Graduate Studies, University of Pennsylvania, 160 BRB II/III - 421 Curie Blvd, Philadelphia, PA, 19104-6064, USA
– name: 3 Department of Biology, University of Pennsylvania, 415 S. University Ave, Philadelphia, PA 19104, USA
– name: 1 Department of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90089, USA
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  surname: Ransick
  fullname: Ransick, Andrew
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  surname: Lindström
  fullname: Lindström, Nils O.
  organization: Department of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90089, USA
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  surname: Liu
  fullname: Liu, Jing
  organization: Department of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90089, USA
– sequence: 4
  givenname: Qin
  surname: Zhu
  fullname: Zhu, Qin
  organization: Graduate Program in Genomics and Computational Biology, Biomedical Graduate Studies, University of Pennsylvania, 160 BRB II/III - 421 Curie Blvd, Philadelphia, PA 19104-6064, USA
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  givenname: Jin-Jin
  surname: Guo
  fullname: Guo, Jin-Jin
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– sequence: 6
  givenname: Gregory F.
  surname: Alvarado
  fullname: Alvarado, Gregory F.
  organization: Department of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90089, USA
– sequence: 7
  givenname: Albert D.
  surname: Kim
  fullname: Kim, Albert D.
  organization: Department of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90089, USA
– sequence: 8
  givenname: Hannah G.
  surname: Black
  fullname: Black, Hannah G.
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  email: amcmahon@med.usc.edu
  organization: Department of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90089, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31689386$$D View this record in MEDLINE/PubMed
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Keywords nephron
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scRNA-Seq profiling
collecting system
lineage convergence
sex differences
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Equal contribution
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AR, APM, NOL, and JL wrote the manuscript. AR, NOL, and JL assembled figures. AR, JL, NOL, HGB and APM designed and/or analyzed experiments. AR and ADK performed single-cell sequencing. JG, NOL, JL and GA performed secondary verification and follow up studies of single cell data predictions. QZ and JK built the interactive web site.
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Snippet Chronic kidney disease affects 10% of the population with notable differences in ethnic and sex-related susceptibility to kidney injury and disease. Kidney...
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SubjectTerms Animals
Cell Lineage
collecting system
Epithelial Cells - cytology
Female
kidney
Kidney - anatomy & histology
Kidney - cytology
lineage convergence
Male
Mice
nephron
Nephrons - cytology
scRNA-Seq profiling
Sex Characteristics
sex differences
Single-Cell Analysis
Time Factors
Title Single-Cell Profiling Reveals Sex, Lineage, and Regional Diversity in the Mouse Kidney
URI https://dx.doi.org/10.1016/j.devcel.2019.10.005
https://www.ncbi.nlm.nih.gov/pubmed/31689386
https://www.proquest.com/docview/2312553526
https://pubmed.ncbi.nlm.nih.gov/PMC6948019
Volume 51
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