Literature DB >> 3525282

Transient expression of collagen type II at epitheliomesenchymal interfaces during morphogenesis of the cartilaginous neurocranium.

P Thorogood, J Bee, K von der Mark.   

Abstract

In the avian embryo a matrix-mediated tissue interaction between retinal pigmented epithelium and neural crest-derived periocular mesenchyme leads to the differentiation of (scleral) cartilage. The composition of the extracellular matrix at the interface between these two tissues has been examined immunohistochemically, both during and after the interaction has taken place. Of the matrix components studied (fibronectin, laminin, and collagen types I, II, IV, and V) only collagen type II displayed a dramatic change in distribution between the two stages. During the interaction, at stage 15, type II was present in the extracellular compartment basal to the epithelium. After completion of the interaction, collagen type II was no longer detectable at the interface even though it was readily detectable in the vitreous humor, cornea, and perinotochordal sheath, and subsequently will be expressed by the chondrogenic tissue itself as overt differentiation commences. These results suggest that collagen type II might be causally involved in this particular epitheliomesenchymal interaction. Examination of the spatial and temporal patterns of collagen type II expression elsewhere in the developing craniofacial complex revealed a hitherto unreported pattern of distribution. In addition to its predictable locations (i.e., cornea, vitreous, and perinotochordal sheath) it was found to be present at certain other sites, for example, at the basal surfaces of some neuroepithelia. These additional locations are all known to be sites of chondrogenesis-promoting tissue interactions which result in the formation of the elements of the cartilaginous neurocranium (e.g., otic vesicle). Furthermore this spatial distribution exhibits a changing temporal pattern in that it is detectable at the time that the interactions are known to be taking place, but subsequently is no longer detectable by the immunohistochemical means employed. This definable pattern of transient collagen type II expression, occurring at very early stages of craniofacial development, is interpreted as reflecting one level of morphogenetic specification of chondrocranial/skull form in the developing vertebrate head.

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Year:  1986        PMID: 3525282     DOI: 10.1016/0012-1606(86)90150-8

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  24 in total

1.  Expression patterns of cartilage collagens and Sox9 during mouse heart development.

Authors:  Otto Rahkonen; Mikko Savontaus; Eltyeb Abdelwahid; Eero Vuorio; Eero Jokinen
Journal:  Histochem Cell Biol       Date:  2003-07-18       Impact factor: 4.304

2.  Chondrogenesis and myogenesis in micromass cultures of mesenchyme from mouse facial primordia.

Authors:  J R Ralphs
Journal:  In Vitro Cell Dev Biol       Date:  1992-05

3.  Spatial and temporal distribution of lamprin mRNA during chondrogenesis of trabecular cartilage in the sea lamprey.

Authors:  K M McBurney; F W Keeley; F S Kibenge; G M Wright
Journal:  Anat Embryol (Berl)       Date:  1996-05

4.  Immunohistochemical investigation of collagen subtypes in human glioblastomas.

Authors:  W Paulus; W Roggendorf; D Schuppan
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1988

5.  Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy).

Authors:  N N Ahmad; L Ala-Kokko; R G Knowlton; S A Jimenez; E J Weaver; J I Maguire; W Tasman; D J Prockop
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-01       Impact factor: 11.205

6.  Type II collagen distribution during cranial development in Xenopus laevis.

Authors:  D W Seufert; J Hanken; M W Klymkowsky
Journal:  Anat Embryol (Berl)       Date:  1994-01

7.  The genesis of cartilage size and shape during development and evolution.

Authors:  B Frank Eames; Richard A Schneider
Journal:  Development       Date:  2008-10-30       Impact factor: 6.868

8.  Mouse Snail family transcription repressors regulate chondrocyte, extracellular matrix, type II collagen, and aggrecan.

Authors:  Kenji Seki; Toshihiko Fujimori; Pierre Savagner; Akiko Hata; Tomonao Aikawa; Naoshi Ogata; Yoichi Nabeshima; Lee Kaechoong
Journal:  J Biol Chem       Date:  2003-08-12       Impact factor: 5.157

Review 9.  A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codon.

Authors:  N N Ahmad; D M McDonald-McGinn; E H Zackai; R G Knowlton; D LaRossa; J DiMascio; D J Prockop
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

10.  Col2-Cre recombinase is co-expressed with endogenous type II collagen in embryonic renal epithelium and drives development of polycystic kidney disease following inactivation of ciliary genes.

Authors:  Elona Kolpakova-Hart; Claudia Nicolae; Jing Zhou; Bjorn R Olsen
Journal:  Matrix Biol       Date:  2008-05-27       Impact factor: 11.583

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