Literature DB >> 8616889

Alternative neural crest cell fates are instructively promoted by TGFbeta superfamily members.

N M Shah1, A K Groves, D J Anderson.   

Abstract

How growth factors influence the fate of multipotent progenitor cells is not well understood. Most hematopoietic growth factors act selectively as survival factors, rather than instructively as lineage determination signals. In the neural crest, neuregulin instructively promotes gliogenesis, but how alternative fates are determined is unclear. We demonstrate that bone morphogenic protein 2 (BMP2) induces the basic-helix-loop-helix protein MASH1 and neurogenesis in neural crest stem cells. In vivo, MASH1+ cells are located near sites of BMP2 mRNA expression. Some smooth muscle differentiation is also observed in BMP2. A related factor, transforming growth factor beta1 (TGFbeta1), exclusively promotes smooth muscle differentiation. Like neuregulin, BMP2 and TGFbeta1 act instructively rather than selectively. The neural crest and hematopoietic systems may therefore utilize growth factors in different ways to generate cellular diversity.

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Year:  1996        PMID: 8616889     DOI: 10.1016/s0092-8674(00)81112-5

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  163 in total

Review 1.  Genes, lineages and the neural crest: a speculative review.

Authors:  D J Anderson
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-07-29       Impact factor: 6.237

2.  Multiple roles of bone morphogenetic protein signaling in the regulation of cortical cell number and phenotype.

Authors:  P C Mabie; M F Mehler; J A Kessler
Journal:  J Neurosci       Date:  1999-08-15       Impact factor: 6.167

3.  Immortalized human dorsal root ganglion cells differentiate into neurons with nociceptive properties.

Authors:  H K Raymon; S Thode; J Zhou; G C Friedman; J R Pardinas; C Barrere; R M Johnson; D W Sah
Journal:  J Neurosci       Date:  1999-07-01       Impact factor: 6.167

4.  Sequential actions of BMP receptors control neural precursor cell production and fate.

Authors:  D M Panchision; J M Pickel; L Studer; S H Lee; P A Turner; T G Hazel; R D McKay
Journal:  Genes Dev       Date:  2001-08-15       Impact factor: 11.361

5.  Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

Authors:  Shiyou Chen; Magdalena Kulik; Robert J Lechleider
Journal:  Nucleic Acids Res       Date:  2003-02-15       Impact factor: 16.971

6.  Trigenic neural crest-restricted Smad7 over-expression results in congenital craniofacial and cardiovascular defects.

Authors:  Sunyong Tang; Paige Snider; Antony B Firulli; Simon J Conway
Journal:  Dev Biol       Date:  2010-05-08       Impact factor: 3.582

7.  Wnt1 and BMP2: two factors recruiting multipotent neural crest progenitors isolated from adult bone marrow.

Authors:  A Glejzer; E Laudet; P Leprince; B Hennuy; C Poulet; O Shakhova; L Sommer; B Rogister; S Wislet-Gendebien
Journal:  Cell Mol Life Sci       Date:  2010-10-26       Impact factor: 9.261

8.  Bmi-1 dependence distinguishes neural stem cell self-renewal from progenitor proliferation.

Authors:  Anna V Molofsky; Ricardo Pardal; Toshihide Iwashita; In-Kyung Park; Michael F Clarke; Sean J Morrison
Journal:  Nature       Date:  2003-10-22       Impact factor: 49.962

9.  Hirschsprung disease is linked to defects in neural crest stem cell function.

Authors:  Toshihide Iwashita; Genevieve M Kruger; Ricardo Pardal; Mark J Kiel; Sean J Morrison
Journal:  Science       Date:  2003-08-15       Impact factor: 47.728

10.  BMP-2 decreases Mash1 stability by increasing Id1 expression.

Authors:  Francesc Viñals; Julia Reiriz; Santiago Ambrosio; Ramon Bartrons; Jose Luis Rosa; Francesc Ventura
Journal:  EMBO J       Date:  2004-08-19       Impact factor: 11.598

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