An extracellular matrix infrastructure provides support for murine secondary palatal shelf remodelling
An extracellular matrix infrastructure provides support for murine secondary palatal shelf remodelling
复制标题
细胞外基质基础设施为小鼠次级腭架重塑提供支持
DOI:
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发表时间:
1992
期刊:
影响因子:
--
通讯作者:
L. Brinkley
中科院分区:
文献类型:
--
作者:
J. Morris;L. Brinkley
A cricial part of secondary palate morphogenesis is the movement of the palatal shelves from an initial vertical position on either side of the tongue to a final horizontal one above it to achieve palate closure. The immunocytochemical localization of extracellular matrix (ECM) molecules in the palatal shelf during this remodelling and reorientation revealed the existence of an ECM infrastructure within the mesenchyme. The major components of this infrastructure were collagen III, fibronectin, and hyaluronate (HA). With remodelling, HA's domain within the mesenchyme was expanded, whereas those of fibronectin and collagen III became more circumscribed. The expansion of an HA‐rich matrix within the mesenchyme is thought to be crucial for palatal reorientation. The results of this study suggest that, as this expansion occurs, it is modulated by collagen and fibronectin components of the ECM infrastructure. Prior to shelf remodelling, this infrastructure may be anchored by a specialized region of the midoral epithelial‐mesenchymal interface and the subjacent mesenchyme which is characterized by the unique distribution of collagen III, fibronectin, and tenascin. The midoral palatal epithelium also may play a role in directing shelf expansion. This epithelial region undergoes changes in cell packing and epithelial cell layering that correlate with shelf remodelling. These changes occur concomitantly with changes in the expression of collagen III, collagen IV, and laminin within the underlying basement membrane. The localization and patterning of tenascin within the developing palate suggests that it not only contributes to the postulated anchoring structure of the midoral epithelial‐mesenchymal region, but also plays a role in the determining the fate of the medial edge epithelial cells during the final stage of palate closure.© Willey‐Liss, Inc.
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DOI:
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发表时间:
1982
期刊:
Journal of embryology and experimental morphology
影响因子:
--
作者:
Brinkley,LL;Vickerman,MM
通讯作者:
Vickerman,MM
DOI:
10.1146/annurev.cb.05.110189.000443
发表时间:
1989-01-01
期刊:
ANNUAL REVIEW OF CELL BIOLOGY
影响因子:
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作者:
ERICKSON, HP;BOURDON, MA
通讯作者:
BOURDON, MA
影响因子:
2.7
作者:
FITCHETT, JE;HAY, ED
通讯作者:
HAY, ED
DOI:
10.1242/dev.100.4.629
发表时间:
1987
期刊:
Development (Cambridge, England)
影响因子:
--
作者:
Brinkley,LL;Morris-Wiman,J
通讯作者:
Morris-Wiman,J