Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2001-7-30
pubmed:abstractText
Sonic Hedgehog (Shh) and Indian Hedgehog (Ihh) are members of the Hedgehog (Hh) family of signaling molecules known to be involved in embryonic patterning and morphogenesis. The Hh proteins undergo an autocatalytic cleavage to yield an N-terminal and a C-terminal peptide, with the signaling capacities confined to the N peptide. Drosophila Hh-N has been shown to act via both short- and long-range signaling. In vertebrates, however, attempts to directly demonstrate Shh (SHH) or Ihh (IHH) proteins at a distance from producing cells have been largely unsuccessful. Furthermore, the fact that the Hh N peptides occur in a cholesterol-modified, membrane-tethered form is not easily reconciled with long-range signaling. This study used optimized immunohistochemistry combined with tissue separation and biochemical analyses in vivo and in vitro to determine the range of action of SHH and IHH in the mouse embryo. In all embryonic structures studied, we detect signaling peptides in producing cells, but we also find that ligands move over considerable distances depending on the tissue. These data provide direct evidence for the presence of Hedgehog signaling peptides in target compartments, suggesting a direct long-range action without a need for secondary mediators. Visualization of Hedgehog proteins in target tissues was achieved only under conditions that allowed proteoglycan/glycosaminoglycan (PG/GAG) preservation. Furthermore, we show that induced changes of the composition of PG/GAG in the tooth alter SHH signaling. These data suggest a crucial role for PG/GAGs in Hedgehog movement.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0012-1606
pubmed:author
pubmed:copyrightInfo
Copyright 2001 Academic Press.
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
236
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
364-86
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:11476578-Animals, pubmed-meshheading:11476578-Calcification, Physiologic, pubmed-meshheading:11476578-Cartilage, pubmed-meshheading:11476578-Cell Differentiation, pubmed-meshheading:11476578-Dental Papilla, pubmed-meshheading:11476578-Diffusion, pubmed-meshheading:11476578-Extracellular Matrix, pubmed-meshheading:11476578-Extremities, pubmed-meshheading:11476578-Gene Deletion, pubmed-meshheading:11476578-Hedgehog Proteins, pubmed-meshheading:11476578-Immunohistochemistry, pubmed-meshheading:11476578-In Situ Hybridization, pubmed-meshheading:11476578-Membrane Proteins, pubmed-meshheading:11476578-Mice, pubmed-meshheading:11476578-Mice, SCID, pubmed-meshheading:11476578-Molecular Weight, pubmed-meshheading:11476578-Odontoblasts, pubmed-meshheading:11476578-Proteoglycans, pubmed-meshheading:11476578-RNA, Messenger, pubmed-meshheading:11476578-Receptors, Cell Surface, pubmed-meshheading:11476578-Signal Transduction, pubmed-meshheading:11476578-Somites, pubmed-meshheading:11476578-Tooth, pubmed-meshheading:11476578-Trans-Activators, pubmed-meshheading:11476578-Transcription, Genetic, pubmed-meshheading:11476578-Up-Regulation
pubmed:year
2001
pubmed:articleTitle
The whereabouts of a morphogen: direct evidence for short- and graded long-range activity of hedgehog signaling peptides.
pubmed:affiliation
Department of Oral Biochemistry, Göteborg University, SE-405 30 Göteborg, Sweden. amel@odontologi.gu.se
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't