Literature DB >> 32586976

Identification and characterization of cellular heterogeneity within the developing renal interstitium.

Alicia R England1,2, Christopher P Chaney1,2, Amrita Das1, Mohita Patel1,3, Alicia Malewska4, Daniel Armendariz5, Gary C Hon5, Douglas W Strand4, Keri A Drake1,3, Thomas J Carroll6,2.   

Abstract

Kidney formation requires the coordinated growth of multiple cell types including the collecting ducts, nephrons, vasculature and interstitium. There is a long-held belief that interactions between progenitors of the collecting ducts and nephrons are primarily responsible for kidney development. However, over the last several years, it has become increasingly clear that multiple aspects of kidney development require signaling from the interstitium. How the interstitium orchestrates these various roles is poorly understood. Here, we show that during development the interstitium is a highly heterogeneous patterned population of cells that occupies distinct positions correlated to the adjacent parenchyma. Our analysis indicates that the heterogeneity is not a mere reflection of different stages in a linear developmental trajectory but instead represents several novel differentiated cell states. Further, we find that β-catenin has a cell autonomous role in the development of a medullary subset of the interstitium and that this non-autonomously affects the development of the adjacent epithelia. These findings suggest the intriguing possibility that the different interstitial subtypes may create microenvironments that play unique roles in development of the adjacent epithelia and endothelia.
© 2020. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Fibroblast heterogeneity; Microenvironment; Patterned interstitium; Patterned stroma; Renal stroma

Mesh:

Year:  2020        PMID: 32586976      PMCID: PMC7438011          DOI: 10.1242/dev.190108

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  58 in total

1.  Pbx1 regulates nephrogenesis and ureteric branching in the developing kidney.

Authors:  Catherine A Schnabel; Robert E Godin; Michael L Cleary
Journal:  Dev Biol       Date:  2003-02-15       Impact factor: 3.582

2.  Advantages of Single-Nucleus over Single-Cell RNA Sequencing of Adult Kidney: Rare Cell Types and Novel Cell States Revealed in Fibrosis.

Authors:  Haojia Wu; Yuhei Kirita; Erinn L Donnelly; Benjamin D Humphreys
Journal:  J Am Soc Nephrol       Date:  2018-12-03       Impact factor: 10.121

3.  Morphogenetic interaction between embryonic mouse tissues separated by a membrane filter.

Authors:  C GROBSTEIN
Journal:  Nature       Date:  1953-11-07       Impact factor: 49.962

4.  Single-cell transcriptomics of the mouse kidney reveals potential cellular targets of kidney disease.

Authors:  Jihwan Park; Rojesh Shrestha; Chengxiang Qiu; Ayano Kondo; Shizheng Huang; Max Werth; Mingyao Li; Jonathan Barasch; Katalin Suszták
Journal:  Science       Date:  2018-04-05       Impact factor: 47.728

5.  Canonical Wnt9b signaling balances progenitor cell expansion and differentiation during kidney development.

Authors:  Courtney M Karner; Amrita Das; Zhendong Ma; Michelle Self; Chuo Chen; Lawrence Lum; Guillermo Oliver; Thomas J Carroll
Journal:  Development       Date:  2011-02-24       Impact factor: 6.868

6.  Fate mapping using Cited1-CreERT2 mice demonstrates that the cap mesenchyme contains self-renewing progenitor cells and gives rise exclusively to nephronic epithelia.

Authors:  Scott Boyle; Andrew Misfeldt; Kelly J Chandler; Karen K Deal; E Michelle Southard-Smith; Douglas P Mortlock; H Scott Baldwin; Mark de Caestecker
Journal:  Dev Biol       Date:  2007-10-24       Impact factor: 3.582

7.  Single-Cell RNA Sequencing of the Adult Mouse Kidney: From Molecular Cataloging of Cell Types to Disease-Associated Predictions.

Authors:  Nils O Lindström; Guilherme De Sena Brandine; Andrew Ransick; Andrew P McMahon
Journal:  Am J Kidney Dis       Date:  2018-09-18       Impact factor: 8.860

8.  Computational assignment of cell-cycle stage from single-cell transcriptome data.

Authors:  Antonio Scialdone; Kedar N Natarajan; Luis R Saraiva; Valentina Proserpio; Sarah A Teichmann; Oliver Stegle; John C Marioni; Florian Buettner
Journal:  Methods       Date:  2015-07-02       Impact factor: 3.608

9.  PAGA: graph abstraction reconciles clustering with trajectory inference through a topology preserving map of single cells.

Authors:  F Alexander Wolf; Fiona K Hamey; Mireya Plass; Jordi Solana; Joakim S Dahlin; Berthold Göttgens; Nikolaus Rajewsky; Lukas Simon; Fabian J Theis
Journal:  Genome Biol       Date:  2019-03-19       Impact factor: 13.583

10.  Stromal-epithelial crosstalk regulates kidney progenitor cell differentiation.

Authors:  Amrita Das; Shunsuke Tanigawa; Courtney M Karner; Mei Xin; Lawrence Lum; Chuo Chen; Eric N Olson; Alan O Perantoni; Thomas J Carroll
Journal:  Nat Cell Biol       Date:  2013-08-25       Impact factor: 28.824

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  23 in total

Review 1.  Determining lineage relationships in kidney development and disease.

Authors:  Melissa H Little; Sara E Howden; Kynan T Lawlor; Jessica M Vanslambrouck
Journal:  Nat Rev Nephrol       Date:  2021-09-30       Impact factor: 28.314

2.  Single-cell and spatial mapping Identify cell types and signaling Networks in the human ureter.

Authors:  Emily E Fink; Surbhi Sona; Uyen Tran; Pierre-Emmanuel Desprez; Matthew Bradley; Hong Qiu; Mohamed Eltemamy; Alvin Wee; Madison Wolkov; Marlo Nicolas; Booki Min; Georges-Pascal Haber; Oliver Wessely; Byron H Lee; Angela H Ting
Journal:  Dev Cell       Date:  2022-07-31       Impact factor: 13.417

3.  Transcription Factors YAP/TAZ and SRF Cooperate To Specify Renal Myofibroblasts in the Developing Mouse Kidney.

Authors:  Keri A Drake; Christopher Chaney; Mohita Patel; Amrita Das; Julia Bittencourt; Martin Cohn; Thomas J Carroll
Journal:  J Am Soc Nephrol       Date:  2022-08-02       Impact factor: 14.978

4.  Stromal Transcription Factor 21 Regulates Development of the Renal Stroma via Interaction with Wnt/β-Catenin Signaling.

Authors:  Gal Finer; Yoshiro Maezawa; Shintaro Ide; Tuncer Onay; Tomokazu Souma; Rizaldy Scott; Xiaoyan Liang; Xiangmin Zhao; Gaurav Gadhvi; Deborah R Winter; Susan E Quaggin; Tomoko Hayashida
Journal:  Kidney360       Date:  2022-05-06

Review 5.  The origin and role of the renal stroma.

Authors:  Sean B Wilson; Melissa H Little
Journal:  Development       Date:  2021-09-23       Impact factor: 6.862

6.  Ret signaling in ureteric bud epithelial cells controls cell movements, cell clustering and bud formation.

Authors:  Adam Packard; William H Klein; Frank Costantini
Journal:  Development       Date:  2021-04-29       Impact factor: 6.868

7.  Smad4 controls proliferation of interstitial cells in the neonatal kidney.

Authors:  Sarah S McCarthy; Michele Karolak; Leif Oxburgh
Journal:  Development       Date:  2022-01-04       Impact factor: 6.868

Review 8.  The Mesangial cell - the glomerular stromal cell.

Authors:  Shimrit Avraham; Ben Korin; Jun-Jae Chung; Leif Oxburgh; Andrey S Shaw
Journal:  Nat Rev Nephrol       Date:  2021-09-10       Impact factor: 28.314

9.  3D Mapping Reveals a Complex and Transient Interstitial Matrix During Murine Kidney Development.

Authors:  Sarah N Lipp; Kathryn R Jacobson; David S Hains; Andrew L Schwarderer; Sarah Calve
Journal:  J Am Soc Nephrol       Date:  2021-04-19       Impact factor: 14.978

Review 10.  Mixing Cells for Vascularized Kidney Regeneration.

Authors:  Michael Namestnikov; Oren Pleniceanu; Benjamin Dekel
Journal:  Cells       Date:  2021-05-06       Impact factor: 6.600

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