Skip to main content
Advertisement

Main menu

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Sign up for alerts
  • About us
    • About Development
    • About the Node
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contacts
    • Subscriptions
    • Feedback
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

User menu

  • Log in
  • Log out

Search

  • Advanced search
Development
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

supporting biologistsinspiring biology

Development

  • Log in
Advanced search

RSS  Twitter  Facebook  YouTube 

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Sign up for alerts
  • About us
    • About Development
    • About the Node
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contacts
    • Subscriptions
    • Feedback
JOURNAL ARTICLES
Stromal cells mediate retinoid-dependent functions essential for renal development
C. Mendelsohn, E. Batourina, S. Fung, T. Gilbert, J. Dodd
Development 1999 126: 1139-1148;
C. Mendelsohn
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
E. Batourina
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
S. Fung
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
T. Gilbert
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
J. Dodd
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & metrics
  • PDF
Loading

Summary

The essential role of vitamin A and its metabolites, retinoids, in kidney development has been demonstrated in vitamin A deficiency and gene targeting studies. Retinoids signal via nuclear transcription factors belonging to the retinoic acid receptor (RAR) and retinoid X receptor (RXR) families. Inactivation of RARaplpha and RARbeta2 receptors together, but not singly, resulted in renal malformations, suggesting that within a given renal cell type, their concerted function is required for renal morphogenesis. At birth, RARalpha beta2(−) mutants displayed small kidneys, containing few ureteric bud branches, reduced numbers of nephrons and lacking the nephrogenic zone where new nephrons are continuously added. These observations have prompted us to investigate the role of RARalpha and RARbeta2 in renal development in detail. We have found that within the embryonic kidney, RARalpha and RARbeta2 are colocalized in stromal cells, but not in other renal cell types, suggesting that stromal cells mediate retinoid-dependent functions essential for renal development. Analysis of RARalpha beta2(−) mutant kidneys at embryonic stages revealed that nephrons were formed and revealed no changes in the intensity or distribution of molecular markers specific for different metanephric mesenchymal cell types. In contrast the development of the collecting duct system was greatly impaired in RARalpha beta2(−) mutant kidneys. Fewer ureteric bud branches were present, and ureteric bud ends were positioned abnormally, at a distance from the renal capsule. Analysis of genes important for ureteric bud morphogenesis revealed that the proto-oncogene c-ret was downregulated. Our results suggest that RARalpha and RARbeta2 are required for generating stromal cell signals that maintain c-ret expression in the embryonic kidney. Since c-ret signaling is required for ureteric bud morphogenesis, loss of c-ret expression is a likely cause of impaired ureteric bud branching in RARalpha beta2(−) mutants.

Reference

    1. Aufderheide E.,
    2. Chiquet-Ehrismann R.,
    3. Ekblom P.
    (1987) Epithelial-mesenchymal interactions in the developing kidney lead to expression of tenascin in the mesenchyme. J. Cell Biol 105, 599–608
    OpenUrlAbstract/FREE Full Text
    1. Bard J.
    (1996) A new role for the stromal cells in kidney development. BioEssays 18, 705–707
    OpenUrlCrossRefPubMedWeb of Science
    1. Chambon P.
    (1996) A decade of molecular biology of retinoic acid receptors. FASEB J 10, 940–954
    OpenUrlAbstract
    1. Dolle P.,
    2. Ruberte E.,
    3. Leroy P.,
    4. Morriss-Kay G.,
    5. Chambon P.
    (1990) Retinoic acid receptors and cellular retinoid binding proteins. I. A systematic study of their differential pattern of transcription during mouse organogenesis. Development 110, 1133–1151
    OpenUrlAbstract/FREE Full Text
    1. Dressler G. R.,
    2. Deutsch U.,
    3. Chowdhury K.,
    4. Nornes H. O.,
    5. Gruss P.
    (1990) Pax2, a new murine paired-box-containing gene and its expression in the developing excretory system. Development 109, 787–795
    OpenUrlAbstract/FREE Full Text
    1. Erickson R. A.
    (1968) Inductive interactions in the development of the mouse metanephros. J. Exp. Zool 169, 33–42
    OpenUrlCrossRefPubMed
    1. Ghyselinck N. B.,
    2. Dupe V.,
    3. Dierich A.,
    4. Messaddeq N.,
    5. Garnier J. M.,
    6. Rochette-Egly C.,
    7. Chambon P.,
    8. Mark M.
    (1997) Role of the retinoic acid receptor beta (RARbeta) during mouse development. Int. J. Dev. Biol 41, 425–447
    OpenUrlPubMedWeb of Science
    1. Giguere V.,
    2. Shago M.,
    3. Zirngibl R.,
    4. Tate P.,
    5. Rossant J.,
    6. Varmuza S.
    (1990) Identification of a novel isoform of the retinoic acid receptor gamma expressed in the mouse embryo. Mol. Cell. Biol 10, 2335–2340
    OpenUrlAbstract/FREE Full Text
    1. Gilbert T.,
    2. Gaonach S.,
    3. Moreau E.,
    4. Merlet-Benichou C.
    (1994) Defect of nephrogenesis by gentamicin in rat metanephric organ culture. Lab. Invest 70, 656–666
    OpenUrlPubMedWeb of Science
    1. Grobstein C.
    (1953) Inductive epithelio-mesenchymal interaction in cultured organ rudiments of the mouse. Science 113, 52–55
    1. Grobstein C.
    (1955) Inductive interaction in the development of the mouse metanephros. J.Exp. Zool 130, 319–340
    OpenUrlCrossRefWeb of Science
    1. Hatini V.,
    2. Huh S. O.,
    3. Herzlinger D.,
    4. Soares V. C.,
    5. Lai E.
    (1996) Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2. Genes Dev 10, 1467–1478
    OpenUrlAbstract/FREE Full Text
    1. Hellmich H. L.,
    2. Kos L.,
    3. Cho E. S.,
    4. Mahon K. A.,
    5. Zimmer A.
    (1996) Embryonic expression of glial cell-line derived neurotrophic factor (GDNF) suggests multiple developmental roles in neural differentiation and epithelial-mesenchymal interactions. Mech. Dev 54, 95–105
    OpenUrlCrossRefPubMedWeb of Science
    1. Herzlinger D.,
    2. Koseki C.,
    3. Mikawa T.,
    4. al-Awqati Q.
    (1992) Metanephric mesenchyme contains multipotent stem cells whose fate is restricted after induction. Development 114, 565–572
    OpenUrlAbstract
    1. Kastner P.,
    2. Mark M.,
    3. Ghyselinck N.,
    4. Krezel W.,
    5. Dupe V.,
    6. Grondona J. M.,
    7. Chambon P.
    (1997) Genetic evidence that the retinoid signal is transduced by heterodimeric RXR/RAR functional units during mouse development. Development 124, 313–326
    OpenUrlAbstract
    1. Kispert A.,
    2. Vainio S.,
    3. Shen L.,
    4. Rowitch D. H.,
    5. McMahon A. P.
    (1996) Proteoglycans are required for maintenance of wnt-11 expression in the ureter tips. Development 122, 3627–3637
    OpenUrlAbstract
    1. Kreidberg J. A.,
    2. Sariola H.,
    3. Loring J. M.,
    4. Maeda M.,
    5. Pelletier J.,
    6. Housman D.,
    7. Jaenisch R.
    (1993) WT1 is required for early kidney development. Cell 74, 679–691
    OpenUrlCrossRefPubMedWeb of Science
    1. Krust A.,
    2. Kastner P.,
    3. Petkovich M.,
    4. Zelent A.,
    5. Chambon P.
    (1989) A third human retinoic acid receptor, hRAR-gamma. Proc. Natl. Acad. Sci. USA 86, 5310–5314
    OpenUrlAbstract/FREE Full Text
    1. Lechner M. S.,
    2. Dressler G. R.
    (1997) The molecular basis of embryonic kidney development. Mech. Dev 62, 105–120
    OpenUrlCrossRefPubMedWeb of Science
    1. Leroy P.,
    2. Krust A.,
    3. Zelent A.,
    4. Mendelsohn C.,
    5. Garnier J. M.,
    6. Kastner P.,
    7. Dierich A.,
    8. Chambon P.
    (1991) Multiple isoforms of the mouse retinoic acid receptor alpha are generated by alternative splicing and differential induction by retinoic acid. EMBO J 10, 59–69
    OpenUrlPubMedWeb of Science
    1. Li E.,
    2. Sucov H. M.,
    3. Lee K. F.,
    4. Evans R. M.,
    5. Jaenisch R.
    (1993) Normal development and growth of mice carrying a targeted disruption of the alpha 1 retinoic acid receptor gene. Proc. Natl. Acad. Sci. USA 90, 1590–1594
    OpenUrlAbstract/FREE Full Text
    1. Lohnes D.,
    2. Mark M.,
    3. Mendelsohn C.,
    4. Dolle P.,
    5. Dierich A.,
    6. Gorry P.,
    7. Gansmuller A.,
    8. Chambon P.
    (1994) Function of the retinoic acid receptors (RARs) during development (I). Craniofacial and skeletal abnormalities in RAR double mutants. Development 120, 2723–2748
    OpenUrlAbstract
    1. Lufkin T.,
    2. Lohnes D.,
    3. Mark M.,
    4. Dierich A.,
    5. Gorry P.,
    6. Gaub M. P.,
    7. LeMeur M.,
    8. Chambon P.
    (1993) High postnatal lethality and testis degeneration in retinoic acid receptor alpha mutant mice. Proc. Natl. Acad. Sci. USA 90, 7225–7229
    OpenUrlAbstract/FREE Full Text
    1. Luo J.,
    2. Sucov H. M.,
    3. Bader J. A.,
    4. Evans R. M.,
    5. Giguere V.
    (1996) Compound mutants for retinoic acid receptor (RAR) beta and RAR alpha 1 reveal developmental functions for multiple RAR beta isoforms. Mech. Dev 55, 33–44
    OpenUrlCrossRefPubMedWeb of Science
    1. Lyons K. M.,
    2. Hogan B. L. M.,
    3. Robertson E. J.
    (1995) Colocalization of Bmp-7 and Bmp-2 RNAs suggests that these factors cooperativelymediate tissue interactions during murine development. Mech. Dev 50, 71–83
    OpenUrlCrossRefPubMedWeb of Science
    1. Mangelsdorf D. J.,
    2. Evans R. M.
    (1995) The RXR heterodimers and orphan receptors. Cell 83, 841–850
    OpenUrlCrossRefPubMedWeb of Science
    1. Mendelsohn C.,
    2. Lohnes D.,
    3. Decimo D.,
    4. Lufkin T.,
    5. LeMeur M.,
    6. Chambon P.,
    7. Mark M.
    (1994) Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants. Development 120, 2749–2771
    OpenUrlAbstract
    1. Mendelsohn C.,
    2. Mark M.,
    3. Dolle P.,
    4. Dierich A.,
    5. Gaub M. P.,
    6. Krust A.,
    7. Lampron C.,
    8. Chambon P.
    (1994) Retinoic acid receptor beta 2 (RAR beta 2) null mutant mice appear normal. Dev. Biol 166, 246–258
    OpenUrlCrossRefPubMedWeb of Science
    1. Moore M. W.,
    2. Klein R. D.,
    3. Farinas I.,
    4. Sauer H.,
    5. Armanini M.,
    6. Phillips H.,
    7. Reichardt L. F.,
    8. Ryans A. M.,
    9. Carver-Moore K.,
    10. Rosenthal A.
    (1996) Renal and neuronal abnormalities in mice lacking GDNF. Nature 382, 76–79
    OpenUrlCrossRefPubMed
    1. Pachnis V.,
    2. Mankoo B.,
    3. Costantini F.
    (1993) Expression of the c-ret proto-oncogene during mouse embryogenesis. Development 119, 1005–1017
    OpenUrlAbstract
    1. Pepicelli C. V.,
    2. Kispert A.,
    3. Rowitch D. H.,
    4. McMahon A. P.
    (1997) GDNF induces branching and increased cell proliferation in the ureter of the mouse. Dev. Biol 192, 193–198
    OpenUrlCrossRefPubMedWeb of Science
    1. Pfaff S. L.,
    2. Mendelsohn M.,
    3. Stewart C. L.,
    4. Edlund T.,
    5. Jessell T. M.
    (1996) Requirement for LIM homeobox gene Isl1 in motor neuron generation reveals a motor neuron-dependent step in interneuron differentiation. Cell 84, 309–320
    OpenUrlCrossRefPubMedWeb of Science
    1. Pichel J. G.,
    2. Shen L.,
    3. Sheng H. Z.,
    4. Granholm A.-C.,
    5. Drago J.,
    6. Grinberg A.,
    7. Lee E. J.,
    8. Huang S. P.,
    9. Saarma M.,
    10. Hoffer B. J.,
    11. Sariola H.,
    12. Westphal H.
    (1996) Defects in enteric innervation and kidney development in mice lacking GDNF. Nature 382, 73–76
    OpenUrlCrossRefPubMed
    1. Rothenpieler U. W.,
    2. Dressler G. R.
    (1993) Pax-2 is required for mesenchyme-to-epithelium conversion during kidney development. Development 119, 711–720
    OpenUrlAbstract/FREE Full Text
    1. Sanicola M.,
    2. Hession C.,
    3. Worley D.,
    4. Carmillo P.,
    5. Ehrenfels C.,
    6. Walus L.,
    7. Robinson S.,
    8. Jaworski G.,
    9. Wei H.,
    10. Tizard R.,
    11. Whitty A.,
    12. Pepinsky R. B.,
    13. Cate R. L.
    (1997) Glial cell line-derived neurotrophic factor-dependent RET activation can be mediated by two different cell-surface accessory proteins. Proc. Natl. Acad. Sci. USA 94, 6238–6243
    OpenUrlAbstract/FREE Full Text
    1. Schuchardt A.,
    2. D'Agati V.,
    3. Larsson-Blomberg L.,
    4. Costantini F.,
    5. Pachnis V.
    (1994) Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 367, 380–383
    OpenUrlCrossRefPubMed
    1. Schuchardt A.,
    2. D'Agati V.,
    3. Pachnis V.,
    4. Costantini F.
    (1996) Renal agenesis and hypodysplasia in ret-kmutant mice result from defects in ureteric bud development. Development 122, 1919–1929
    OpenUrlAbstract
    1. Stark K.,
    2. Vainio S.,
    3. Vassileva G.,
    4. McMahon A. P.
    (1994) Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4. Nature 372, 679–683
    OpenUrlCrossRefPubMed
    1. Treanor J.,
    2. Goodman L.,
    3. de Sauvage F.,
    4. Stone D.,
    5. Poulsen K.,
    6. Beck C.,
    7. Gray C.,
    8. Armanini M.,
    9. Pollock R.,
    10. Hefti F.,
    11. Phillips H.,
    12. Goddard A.,
    13. Moore M.,
    14. Buj-Bello A.,
    15. Davies A.,
    16. Asai N.,
    17. Takahashi M.,
    18. Vandlen R.,
    19. Henderson C.,
    20. Rosenthal A.
    (1996) Characterization of a multicomponent receptor for GDNF. Nature 382, 80–83
    OpenUrlCrossRefPubMed
    1. Vilar J.,
    2. Gilbert T.,
    3. Moreau E.,
    4. Merlet-Benichou C.
    (1996) Metanephros organogenesis is highly stimulated by vitamin A derivatives in organ culture. Kidney Int 49, 1478–1487
    OpenUrlPubMedWeb of Science
    1. Wilson J. G.,
    2. Warkany J.
    (1948) Malformations in the genito-urinary tract induced by maternal vitamin A deficiency in the rat. Am. J. Anat 83, 357–407
    OpenUrlCrossRefPubMedWeb of Science
    1. Zelent A.,
    2. Krust A.,
    3. Petkovich M.,
    4. Kastner P.,
    5. Chambon P.
    (1989) Cloning of murine alpha and beta retinoic acid receptors and a novel receptor gamma predominantly expressed in skin. Nature 339, 714–717
    OpenUrlCrossRefPubMed
    1. Zelent A.,
    2. Mendelsohn C.,
    3. Kastner P.,
    4. Krust A.,
    5. Garnier J. M.,
    6. Ruffenach F.,
    7. Leroy P.,
    8. Chambon P.
    (1991) Differentially expressed isoforms of the mouse retinoic acid receptor beta generated by usage of two promoters and alternative splicing. EMBO J 10, 71–81
    OpenUrlPubMedWeb of Science
Previous ArticleNext Article
Back to top
Previous ArticleNext Article

This Issue

 Download PDF

Email

Thank you for your interest in spreading the word on Development.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Stromal cells mediate retinoid-dependent functions essential for renal development
(Your Name) has sent you a message from Development
(Your Name) thought you would like to see the Development web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
JOURNAL ARTICLES
Stromal cells mediate retinoid-dependent functions essential for renal development
C. Mendelsohn, E. Batourina, S. Fung, T. Gilbert, J. Dodd
Development 1999 126: 1139-1148;
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
Citation Tools
JOURNAL ARTICLES
Stromal cells mediate retinoid-dependent functions essential for renal development
C. Mendelsohn, E. Batourina, S. Fung, T. Gilbert, J. Dodd
Development 1999 126: 1139-1148;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Alerts

Please log in to add an alert for this article.

Sign in to email alerts with your email address

Article navigation

  • Top
  • Article
  • Info & metrics
  • PDF

Related articles

Cited by...

More in this TOC section

  • A BAC transgenic analysis of the Mrf4/Myf5 locus reveals interdigitated elements that control activation and maintenance of gene expression during muscle development
  • Visualization and functional characterization of the developing murine cardiac conduction system
  • Indian hedgehog activates hematopoiesis and vasculogenesis and can respecify prospective neurectodermal cell fate in the mouse embryo
Show more JOURNAL ARTICLES

Similar articles

Other journals from The Company of Biologists

Journal of Cell Science

Journal of Experimental Biology

Disease Models & Mechanisms

Biology Open

Advertisement

Kathryn Virginia Anderson (1952-2020)

Developmental geneticist Kathryn Anderson passed away at home on 30 November 2020. Tamara Caspary, a former postdoc and friend, remembers Kathryn and her remarkable contribution to developmental biology.


Zooming into 2021

In a new Editorial, Editor-in-Chief James Briscoe and Executive Editor Katherine Brown reflect on the triumphs and tribulations of the last 12 months, and look towards a hopefully calmer and more predictable year.


Read & Publish participation extends worldwide

Over 60 institutions in 12 countries are now participating in our Read & Publish initiative. Here, James Briscoe explains what this means for his institution, The Francis Crick Institute. Find out more and view our full list of participating institutions.


Upcoming special issues

Imaging Development, Stem Cells and Regeneration
Submission deadline: 30 March 2021
Publication: mid-2021

The Immune System in Development and Regeneration
Guest editors: Florent Ginhoux and Paul Martin
Submission deadline: 1 September 2021
Publication: Spring 2022

Both special issues welcome Review articles as well as Research articles, and will be widely promoted online and at key global conferences.


Development presents...

Our successful webinar series continues into 2021, with early-career researchers presenting their papers and a chance to virtually network with the developmental biology community afterwards. Sign up to join our next session:

10 February
Time: 13:00 (GMT)
Chaired by: preLights

Articles

  • Accepted manuscripts
  • Issue in progress
  • Latest complete issue
  • Issue archive
  • Archive by article type
  • Special issues
  • Subject collections
  • Sign up for alerts

About us

  • About Development
  • About the Node
  • Editors and board
  • Editor biographies
  • Travelling Fellowships
  • Grants and funding
  • Journal Meetings
  • Workshops
  • The Company of Biologists

For authors

  • Submit a manuscript
  • Aims and scope
  • Presubmission enquiries
  • Article types
  • Manuscript preparation
  • Cover suggestions
  • Editorial process
  • Promoting your paper
  • Open Access
  • Biology Open transfer

Journal info

  • Journal policies
  • Rights and permissions
  • Media policies
  • Reviewer guide
  • Sign up for alerts

Contact

  • Contact Development
  • Subscriptions
  • Advertising
  • Feedback

 Twitter   YouTube   LinkedIn

© 2021   The Company of Biologists Ltd   Registered Charity 277992