Literature DB >> 1707785

T-cadherin expression alternates with migrating neural crest cells in the trunk of the avian embryo.

B Ranscht1, M Bronner-Fraser.   

Abstract

Trunk neural crest cells and motor axons move in a segmental fashion through the rostral (anterior) half of each somitic sclerotome, avoiding the caudal (posterior) half. This metameric migration pattern is thought to be caused by molecular differences between the rostral and caudal portions of the somite. Here, we describe the distribution of T-cadherin (truncated-cadherin) during trunk neural crest cell migration. T-cadherin, a novel member of the cadherin family of cell adhesion molecules was selectively expressed in the caudal half of each sclerotome at all times examined. T-cadherin immunostaining appeared graded along the rostrocaudal axis, with increasing levels of reactivity in the caudal halves of progressively more mature (rostral) somites. The earliest T-cadherin expression was detected in a small population of cells in the caudal portion of the somite three segments rostral to last-formed somite. This initial T-cadherin expression was observed concomitant with the invasion of the first neural crest cells into the rostral portion of the same somite in stage 16 embryos. When neural crest cells were ablated surgically prior to their emigration from the neural tube, the pattern of T-cadherin immunoreactivity was unchanged compared to unoperated embryos, suggesting that the metameric T-cadherin distribution occurs independent of neural crest cell signals. This expression pattern is consistent with the possibility that T-cadherin plays a role in influencing the pattern of neural crest cell migration and in maintaining somite polarity.

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Year:  1991        PMID: 1707785     DOI: 10.1242/dev.111.1.15

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


  29 in total

1.  Ephrin-as cooperate with EphA4 to promote trunk neural crest migration.

Authors:  R McLennan; C E Krull
Journal:  Gene Expr       Date:  2002

Review 2.  Motor axon pathfinding.

Authors:  Dario Bonanomi; Samuel L Pfaff
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-03       Impact factor: 10.005

Review 3.  Regional differences in neural crest morphogenesis.

Authors:  Bryan R Kuo; Carol A Erickson
Journal:  Cell Adh Migr       Date:  2010 Oct-Dec       Impact factor: 3.405

Review 4.  Mechanisms driving neural crest induction and migration in the zebrafish and Xenopus laevis.

Authors:  Michael W Klymkowsky; Christy Cortez Rossi; Kristin Bruk Artinger
Journal:  Cell Adh Migr       Date:  2010 Oct-Dec       Impact factor: 3.405

Review 5.  In the beginning: Generating neural crest cell diversity.

Authors:  Christiana Ruhrberg; Quenten Schwarz
Journal:  Cell Adh Migr       Date:  2010 Oct-Dec       Impact factor: 3.405

6.  A segmented pattern of cell death during development of the chick embryo.

Authors:  P Jeffs; M Osmond
Journal:  Anat Embryol (Berl)       Date:  1992

7.  T-cadherin is critical for adiponectin-mediated cardioprotection in mice.

Authors:  Martin S Denzel; Maria-Cecilia Scimia; Philine M Zumstein; Kenneth Walsh; Pilar Ruiz-Lozano; Barbara Ranscht
Journal:  J Clin Invest       Date:  2010-12       Impact factor: 14.808

8.  The fate of somitocoele cells in avian embryos.

Authors:  R Huang; Q Zhi; J Wilting; B Christ
Journal:  Anat Embryol (Berl)       Date:  1994-09

9.  Expression of M-cadherin, a member of the cadherin multigene family, correlates with differentiation of skeletal muscle cells.

Authors:  M Donalies; M Cramer; M Ringwald; A Starzinski-Powitz
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-15       Impact factor: 11.205

10.  Identification of T-cadherin as a novel target of DNA methyltransferase 3B and its role in the suppression of nerve growth factor-mediated neurite outgrowth in PC12 cells.

Authors:  Shoumei Bai; Kalpana Ghoshal; Samson T Jacob
Journal:  J Biol Chem       Date:  2006-03-14       Impact factor: 5.157

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