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
Avian neural crest cells can migrate in the dorsolateral path only if they are specified as melanocytes
C.A. Erickson, T.L. Goins
Development 1995 121: 915-924;
C.A. Erickson
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
T.L. Goins
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & metrics
  • PDF
Loading

Summary

Neural crest cells are conventionally believed to migrate arbitrarily into various pathways and to differentiate according to the environmental cues that they encounter. We present data consistent with the notion that melanocytes are directed, by virtue of their phenotype, into the dorsolateral path, whereas other neural crest derivatives are excluded. In the avian embryo, trunk neural crest cells that migrate ventrally differentiate largely into neurons and glial cells of the peripheral nervous system. Neural crest cells that migrate into the dorsolateral path become melanocytes, the pigment cells of the skin. Neural crest cells destined for the dorsolateral path are delayed in their migration until at least 24 hours after migration commences ventrally. Previous studies have suggested that invasion into the dorsolateral path is dependent upon a change in the migratory environment. A complementary possibility is that as neural crest cells differentiate into melanocytes they acquire the ability to take this pathway. When quail neural crest cells that have been grown in culture for 12 hours are labeled with Fluoro-gold and then grafted into the early migratory pathway at the thoracic level, they migrate only ventrally and are coincident with the host neural crest. When fully differentiated melanocytes (96 hours old) are back-grafted under identical conditions, however, they enter the dorsolateral path and invade the ectoderm at least one day prior to the host neural crest. Likewise, neural crest cells that have been cultured for at least 20 hours and are enriched in melanoblasts immediately migrate in the dorsolateral path, in addition to the ventral path, when back-grafted into the thoracic level. A population of neural crest cells depleted of melanoblasts--crest cells derived from the branchial arches--are not able to invade the dorsolateral path, suggesting that only pigment cells or their precursors are able to take this migratory route. These results suggest that as neural crest cells differentiate into melanocytes they can exploit the dorsolateral path immediately. Even when 12-hour crest cells are grafted into stage 19–21 embryos at an axial level where host crest are invading the dorsolateral path, these young neural crest cells do not migrate dorsolaterally. Conversely, melanoblasts or melanocytes grafted under the same circumstances are found in the ectoderm. These latter results suggest that during normal development neural crest cells must be specified, if not already beginning to differentiate, as melanocytes in order to take this path.(ABSTRACT TRUNCATED AT 400 WORDS)

Reference

    1. Artinger K. B.,
    2. Bronner-Fraser M.
    (1992) Partial restriction in the developmental potential of late emigrating avian neural crest cells. Dev. Biol 149, 149–157
    OpenUrlCrossRefPubMed
    1. Ayer-Le Lievre C. S.,
    2. Le Douarin N. M.
    (1982) The early development of cranial sensory ganglia and the potentialities of their component cells studied in quail-chick chimeras. Dev. Biol 94, 291–310
    OpenUrlCrossRefPubMedWeb of Science
    1. Bronner M. E.,
    2. Cohen A. M.
    (1979) Migratory patterns of cloned neural crest melanocytes injected into host chicken embryos. Proc. Nat. Acad. Sci. USA 76, 1843–1848
    OpenUrlAbstract/FREE Full Text
    1. Bronner-Fraser M.,
    2. Cohen A. M.
    (1980) Analysis of the neural crest ventral pathway using injected tracer cells. Dev. Biol 77, 130–141
    OpenUrlCrossRefPubMed
    1. Bronner-Fraser M.,
    2. Sieber-Blum M.,
    3. Cohen A. M.
    (1980) Clonal analysis of the avian neural crest: migration and maturation of mixed neural crest clones injected into host chicken embryos. J. Comp. Neurol 193, 423–434
    OpenUrlCrossRefPubMed
    1. Ciment G.,
    2. Weston J. A.
    (1983) Enteric neurogenesis by neural crest-derived branchial arch mesenchymal cells. Nature 305, 424–427
    OpenUrlCrossRefPubMed
    1. Coulombe J. N.,
    2. Bronner-Fraser M.
    (1986) Cholinergic neurons acquire adrenergic neurotransmitters when transplanted into an embryo. Nature 324, 569–572
    OpenUrlCrossRefPubMed
    1. Cudennec C.
    (1977) Reconnaissances cellulaires au cours du developpement: etude in vivo au moyen de chimeres interspecifiques chez l'embryon d'oiseau. Biol. Cell 30, 41–48
    OpenUrl
    1. Duband J.-L.,
    2. Dufour S.,
    3. Yamada S. S.,
    4. Yamada K. M.,
    5. Thiery J. P.
    (1991) Neural crest cell locomotion induced by antibodies to β1 integrins. J. Cell Sci 98, 517–532
    OpenUrlAbstract/FREE Full Text
    1. Dupin E.
    (1984) Cell division in the ciliary ganglion of quail embryos in situ and after back-transplantation into the neural crest migration pathways of chick embryos. Dev. Biol 105, 288–299
    OpenUrlCrossRefPubMedWeb of Science
    1. Erickson C. A.
    (1985) Control of neural crest cell dispersion in the trunk of the avian embryo. Dev. Biol 111, 138–157
    OpenUrlCrossRefPubMedWeb of Science
    1. Erickson C. A.
    (1987) Behavior of neural crest cells on embryonic basal laminae. Dev. Biol 120, 38–49
    OpenUrlCrossRefPubMed
    1. Erickson C. A.
    (1993) From the crest to the periphery: control of pigment cell migration and lineage segregation. Pigment Cell Res 6, 336–347
    OpenUrlCrossRefPubMedWeb of Science
    1. Erickson C. A.,
    2. Tosney K. W.,
    3. Weston J. A.
    (1980) Analysis of migratory behavior of neural crest and fibroblastic cells in embryonic tissues. Dev. Biol 77, 142–156
    OpenUrlCrossRefPubMedWeb of Science
    1. Erickson C. A.,
    2. Duong T. D.,
    3. Tosney K. W.
    (1992) Descriptive and experimental analysis of the dispersion of neural crest cells along the dorsolateral path and their entry into ectoderm in the chick embryo. Dev. Biol 151, 251–272
    OpenUrlCrossRefPubMedWeb of Science
    1. Glimelius B.,
    2. Weston J. A.
    (1981) Analysis of developmentally homogeneous neural crest cell populations in vitro. II. A tumor-promoter (TPA) delays differentiation and promotes cell proliferation. Dev. Biol 82, 95–101
    OpenUrlCrossRefPubMed
    1. Halaban R.,
    2. Langdon R.,
    3. Birchall N.,
    4. Cuono C.,
    5. Baird A.,
    6. Scott G.,
    7. Moellmann G.,
    8. McGuire J.
    (1988) Basic fibroblast growth factor from human keratinocytes is a natural mitogen for melanocytes. J. Cell Biol 107, 1611–1619
    OpenUrlAbstract/FREE Full Text
    1. Hamburger V.,
    2. Hamilton H. L.
    (1951) A series of normal stages in the development of the chick embryo. J. Morph 88, 49–92
    OpenUrlCrossRefPubMedWeb of Science
    1. Hirata T.,
    2. Mori E.,
    3. Morimoto M.,
    4. Kasugai T.,
    5. Tsujimura T.,
    6. Hirota S.,
    7. Kanakura Y.,
    8. Nomura S.,
    9. Kitamura Y.
    (1993) Stem cell factor induces positive outgrowth of c-kit-positive neurites and supports the survival of c-kit-positive neurons in dorsal root ganglia of mouse embryos. Development 119, 49–56
    OpenUrlAbstract
    1. Ito K.,
    2. Sieber-Blum M.
    (1993) Pluripotent and developmentally restricted neural-crest-derived cells in posterior visceral arches. Dev. Biol 156, 191–200
    OpenUrlCrossRefPubMedWeb of Science
    1. Kalcheim C.,
    2. Neufeld G.
    (1990) Expression of basic fibroblast growth factor in the nervous system of early avian embryos. Development 109, 203–215
    OpenUrlAbstract
    1. Keshet E.,
    2. Lyman S. D.,
    3. Williams D. E.,
    4. Anderson D. M.,
    5. Jenkins N. A.,
    6. Copeland N. G.,
    7. Parada L. F.
    (1991) Embryonic RNA expression patterns of the c- kit receptor and its cognate ligand suggest multiple functional roles in mouse development. EMBO J 10, 2425–2435
    OpenUrlPubMedWeb of Science
    1. Kirby M. L.,
    2. Kumiski D. H.,
    3. Myers T.,
    4. Cerjan C.,
    5. Mishima N.
    (1993) Backtransplantation of chick cardiac neural crest cells cultured in LIF rescues heart development. Dev. Dynamics 198, 296–311
    OpenUrlPubMedWeb of Science
    1. Kitamura K.,
    2. Takiguchi-Hayashi K.,
    3. Sezaki M.,
    4. Yamamoto H.,
    5. Takeuchi T.
    (1992). Avian neural crest cells express a melanogenic trait during early migration from the neural tube: observations with the new monoclonal antibody, ‘MEBL-1.’. Development 114, 367–378
    OpenUrlAbstract
    1. Le Douarin N. M.
    (1986) Cell line segregation during peripheral nervous system ontogeny. Science 231, 1515–1522
    OpenUrlAbstract/FREE Full Text
    1. Le Douarin N. M.,
    2. Teillet M. A.
    (1973) The migration of neural crest cells to the wall of the digestive tract in avian embryo. J. Embryol. Exp. Morphol 30, 31–48
    OpenUrlPubMedWeb of Science
    1. Le Douarin N. M.,
    2. Teillet M.-A.
    (1974) Experimental analysis of the migration and differentiation of neuroblasts of the autonomic nervous system and of neuroectodermal mesenchymal derivatives, using a biological cell marking technique. Dev. Biol 41, 162–184
    OpenUrlCrossRefPubMedWeb of Science
    1. Le Douarin N. M.,
    2. Ziller C.,
    3. Couly G. F.
    (1993) Patterning of neural crest derivatives in the avian embryo: in vivo and in vitro studies. Dev. Biol 159, 24–49
    OpenUrlCrossRefPubMedWeb of Science
    1. Le Douarin N. M.,
    2. Renaud D.,
    3. Teillet M.-A.,
    4. Le Douarin G. H.
    (1975) Cholinergic differentiation of presumptive adrenergic neuroblasts in interspecific chimaeras after heterotopic transplantations. Proc. Natl. Acad. Sci. USA 72, 728–732
    OpenUrlAbstract/FREE Full Text
    1. Le Douarin N. M.,
    2. Teillet M. A.,
    3. Ziller C.,
    4. Smith J.
    (1978) Adrenergic differentiation of cells of the cholinergic ciliary and Remak ganglia in avian embryo after in vivo transplantation. Proc. Natl. Acad. Sci. USA 75, 2030–2034
    OpenUrlAbstract/FREE Full Text
    1. Le Lievre C. S.,
    2. Schweizer G. G.,
    3. Ziller C. M.,
    4. Le Douarin N. M.
    (1980) Restrictions of developmental capabilities in neural crest cell derivatives as tested by invivotransplantation experiments. Dev. Biol 77, 362–378
    OpenUrlCrossRefPubMedWeb of Science
    1. Loring J. F.,
    2. Erickson C. A.
    (1987) Neural crest cell migratory pathways in the trunk of the chick embryo. Dev. Biol 121, 220–236
    OpenUrlCrossRefPubMedWeb of Science
    1. Loring J.,
    2. Glimelius B.,
    3. Erickson C.,
    4. Weston J. A.
    (1981) Analysis of developmentally homogeneous neural crest cell populations in vitro. I. Formation, morphology and differentiative behavior. Dev. Biol 82, 86–94
    OpenUrlCrossRefPubMed
    1. Manova K.,
    2. Bacharova R. F.
    (1991) Expression of c-kit encoded at the W locus of mice in developing embryonic germ cells and presumptive melanoblasts. Dev. Biol 146, 312–324
    OpenUrlCrossRefPubMedWeb of Science
    1. Marusich M. F.,
    2. Weston J. A.
    (1992) Identification of early neurogenic cells in the neural crest lineage. Dev. Biol 149, 295–306
    OpenUrlCrossRefPubMedWeb of Science
    1. Meininger C. J.,
    2. Yano H.,
    3. Rottapel R.,
    4. Bernstein A.,
    5. Zsebo K. M.,
    6. Zetter B. R.
    (1992) The c-kit receptor ligand functions as a mast cell chemoattractant. Blood 79, 958–963
    OpenUrlAbstract/FREE Full Text
    1. Motro B.,
    2. Van der Kooy D.,
    3. Rossant J.,
    4. Reith A.,
    5. Bernstein A.
    (1991) Contiguous patterns of c- kit and steel expression: analysis of mutations at the W and Sl loci. Development 113, 1207–1221
    OpenUrlAbstract
    1. Oakley R. A.,
    2. Lasky C. J.,
    3. Erickson C. A.,
    4. Tosney K. W.
    (1994) Glycoconjugates mark a transient barrier to neural crest migration in the chicken embryo. Development 120, 103–114
    OpenUrlAbstract
    1. Orr-Urtreger A.,
    2. Avivi A.,
    3. Zimmer Y.,
    4. Givol D.,
    5. Yarden Y.,
    6. Lonai P.
    (1990) Developmental expression of c- kit, a proto-oncogene encoded by the W locus. Development 109, 911–923
    OpenUrlAbstract/FREE Full Text
    1. Pavan W. J.,
    2. Tilghman S. M.
    (1994) Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes. Proc. Natl. Acad. Sci. USA 91, 7159–7163
    OpenUrlAbstract/FREE Full Text
    1. Perris R.,
    2. Löfberg J.
    (1986) Promotion of chromatophore differentiation in isolated premigratory neural crest cells by extracellular material explanted on microcarriers. Dev. Biol 113, 327–341
    OpenUrlCrossRefPubMedWeb of Science
    1. Qian F.,
    2. Vaux D. L.,
    3. Weissman I. L.
    (1994) Expression of the integrin4 1 on melanoma cells can inhibit the invasive stage of metastasis formation. Cell 77, 335–347
    OpenUrlCrossRefPubMedWeb of Science
    1. Raible D. W.,
    2. Eisen J. S.
    (1994) Restriction of neural crest cell fate in the trunk of the embryonic zebrafish. Development 120, 495–503
    OpenUrlAbstract
    1. Richardson M. K.,
    2. Sieber-Blum M.
    (1993) Pluripotent neural crest cells in the developing skin of the quail embryo. Dev. Biol 157, 348–358
    OpenUrlCrossRefPubMed
    1. Rogers S. L.,
    2. Bernard L.,
    3. Weston J. A.
    (1990) Substratum effects on cell dispersal, morphology, and differentiation in cultures of avian neural crest cells. Dev. Biol 141, 173–182
    OpenUrlCrossRefPubMed
    1. Rothman T. P.,
    2. Le Douarin N. M.,
    3. Fontaine-Perus J. C.,
    4. Gershon M. D.
    (1990) Developmental potential of neural crest-derived cells migrating from segments of developing quail bowel back-grafted into younger chick host embryos. Development 109, 411–423
    OpenUrlAbstract
    1. Savage M. P.,
    2. Hart C. E.,
    3. Riley B. B.,
    4. Sasse J.,
    5. Olwin B. B.,
    6. Fallon J. F.
    (1993) Distribution of FGF-2 suggests it has a role in chick limb bud growth. Dev. Dynamics 198, 159–170
    OpenUrlCrossRefPubMedWeb of Science
    1. Sears R.,
    2. Ciment G.
    (1988) Changes in the migratory properties of neural crest and early crest-derived cells in vivo following treatment with a phorbol ester drug. Dev. Biol 130, 133–143
    OpenUrlCrossRefPubMed
    1. Selleck M. A. J.,
    2. Scherson T. Y.,
    3. Bronner-Fraser M.
    (1993) Origins of neural crest cell diversity. Dev. Biol 159, 1–11
    OpenUrlCrossRefPubMedWeb of Science
    1. Serbedzija G. N.,
    2. Bronner-Fraser M.,
    3. Fraser S. E.
    (1989) A vital dye analysis of the timing and pathways of neural crest cell migration. Development 106, 809–819
    OpenUrlAbstract/FREE Full Text
    1. Serbedzija G. N.,
    2. Fraser S.,
    3. Bronner-Fraser M.
    (1990) Pathways of trunk neural crest cell migration in the mouse embryo as revealed by vital dye labelling. Development 108, 605–612
    OpenUrlAbstract/FREE Full Text
    1. Sieber-Blum M.,
    2. Cohen A. M.
    (1980) Clonal analysis of quail neural crest cells: they are pluripotent and differentiate in vitro in the absence of non-crest cells. Dev. Biol 80, 96–106
    OpenUrlCrossRefPubMedWeb of Science
    1. Sieber-Blum M.,
    2. Sieber F.,
    3. Yamada K. M.
    (1981) Cellular fibronectin promotes adrenergic differentiation of quail neural crest cells in vitro. Exp. Cell Res 133, 285–295
    OpenUrlCrossRefPubMed
    1. Steel K. P.,
    2. Davidson D. R.,
    3. Jackson I. J.
    (1992) TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor. Development 115, 1111–1119
    OpenUrlAbstract
    1. Stemple D. L.,
    2. Anderson D. J.
    (1993) Lineage diversification of the neural crest: in vitro investigations. Dev. Biol 159, 12–23
    OpenUrlCrossRefPubMedWeb of Science
    1. Stocker K. M.,
    2. Sherman L.,
    3. Rees S.,
    4. Ciment G.
    (1991) Basic FGF and TGF-β1 influence commitment to melanogenesis in neural crest-derived cells of avian embryos. Development 111, 635–645
    OpenUrlAbstract
    1. Thiery J. P.,
    2. Duband J. L.,
    3. Delouvee A.
    (1982) Pathways and mechanisms of avian trunk neural crest cell migration and localization. Dev. Biol 93, 324–343
    OpenUrlCrossRefPubMedWeb of Science
    1. Tosney K. W.
    (1992) A long-distance cue from emerging dermis stimulates neural crest migration. Soc. Neurosci. Abs.
    1. Tucker R. P.,
    2. Erickson C. A.
    (1986). Pigment cell pattern formation in Taricha torosa: the role of the extracellular matrix in controlling pigment cell migration and differentiation. Dev. Biol 118, 268–285
    OpenUrlCrossRefPubMedWeb of Science
    1. Vogel K. S.,
    2. Weston J. A.
    (1988) A subpopulation of cultured avian neural crest cells has transient neurogenic potential. Neuron 1, 569–577
    OpenUrlCrossRefWeb of Science
    1. Weiss P.,
    2. Andres G.
    (1952) Experiments on the fate of embryonic cells (chick) disseminated by the vascular route. J. Exp. Zool 121, 449–487
    OpenUrl
    1. Weston J. A.
    (1991) Sequential segregation and fate of developmentally restricted intermediate cell populations in the neural crest lineage. Curr. Topics Dev. Biol 23, 133–153
    OpenUrlAbstract/FREE Full Text
    1. Zambruno G.,
    2. Marchisio P. C.,
    3. Melchiori A.,
    4. Bondanza S.,
    5. Cancedda R.,
    6. De Luca M.
    (1993) Expression of integrin receptors and their role in adhesion, spreading and migration of normal human melanocytes. J. Cell Sci 105, 179–190
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.
Avian neural crest cells can migrate in the dorsolateral path only if they are specified as melanocytes
(Your Name) has sent you a message from Development
(Your Name) thought you would like to see the Development web site.
Share
JOURNAL ARTICLES
Avian neural crest cells can migrate in the dorsolateral path only if they are specified as melanocytes
C.A. Erickson, T.L. Goins
Development 1995 121: 915-924;
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
Citation Tools
JOURNAL ARTICLES
Avian neural crest cells can migrate in the dorsolateral path only if they are specified as melanocytes
C.A. Erickson, T.L. Goins
Development 1995 121: 915-924;

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

  • Non-imprinted Igf2r expression decreases growth and rescues the Tme mutation in mice
  • REF-1, a protein with two bHLH domains, alters the pattern of cell fusion in C. elegans by regulating Hox protein activity
  • The dermomyotome dorsomedial lip drives growth and morphogenesis of both the primary myotome and dermomyotome epithelium
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

Interviews — Bénédicte Sanson and Kate Storey

Bénédicte Sanson and Kate Storey

Hear from Bénédicte Sanson, winner of the BSDB’s Cheryll Tickle medal, and Kate Storey, winner of the BSDB’s Waddington Medal, as they discuss their research, the future of the field and the importance of collaboration.


Review Commons launches

We're excited to be an affiliate journal for Review Commons, the ASAPbio/EMBO platform for high-quality journal-independent peer-review in the life sciences, which went live on 09 December.


Have you heard about our Travelling Fellowships?

Peter Baillie-Johnson in Switzerland

Early-career researchers can apply for up to £2,500 to offset the cost of travel and expenses to make collaborative visits to other labs around the world. Read about Peter’s experience in Switzerland, where he joined forces with the Lutolf lab to refine a protocol for producing gastruloids.


Publishing peer review reports

To continue working towards transparency around the editorial process, Development now publishes a ‘Peer review history file’ alongside published papers. Read more about the policy and see the reports for yourself in one the first papers to publish the reports (under the ‘Info & metrics’ tab).


Development at a glance — Cell interactions in collective cell migration

Extract from the poster showing specific cell-cell interactions in metastasis.

Take a look at the latest poster and accompanying article by Denise Montell and her colleagues from the University of California, where they describe a sampling of both known and new cells that migrate collectively in vivo.

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

© 2019   The Company of Biologists Ltd   Registered Charity 277992