A unique form of collective epithelial migration is crucial for tissue fusion in the secondary palate and can overcome loss of epithelial apoptosis.
A unique form of collective epithelial migration is crucial for tissue fusion in the secondary palate and can overcome loss of epithelial apoptosis.
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一种独特形式的集体上皮迁移是至关重要的组织融合在继发腭,可以克服上皮细胞凋亡的损失。
DOI:
10.1242/dev.200181
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发表时间:
2022-05-15
期刊:
影响因子:
--
通讯作者:
中科院分区:
文献类型:
--
作者:
Tissue fusion frequently requires the removal of an epithelium that intervenes distinct primordia to form one continuous structure. In the mammalian secondary palate, a midline epithelial seam (MES) forms between two palatal shelves and must be removed to allow mesenchymal confluence. Abundant apoptosis and cell extrusion support their importance in MES removal. However, genetically disrupting the intrinsic apoptotic regulators BAX and BAK within the MES results in complete loss of cell death and cell extrusion, but successful removal of the MES. Novel static- and live-imaging approaches reveal that the MES is removed through streaming migration of epithelial trails and islands to reach the oral and nasal epithelial surfaces. Epithelial trail cells that express the basal epithelial marker ΔNp63 begin to express periderm markers, suggesting that migration is concomitant with differentiation. Live imaging reveals anisotropic actomyosin contractility within epithelial trails, and genetic ablation of actomyosin contractility results in dispersion of epithelial collectives and failure of normal MES migration. These findings demonstrate redundancy between cellular mechanisms of morphogenesis, and reveal a crucial and unique form of collective epithelial migration during tissue fusion. Summary: Multiple cellular processes mediate secondary palate fusion, including a unique form of streaming collective epithelial migration driven by pulsatile actomyosin contractility.
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影响因子:
4.6
作者:
Cuervo, R;Covarrubias, L
通讯作者:
Covarrubias, L
影响因子:
3.3
作者:
Blavier, L;Lazaryev, A;Kaartinen, V
通讯作者:
Kaartinen, V
影响因子:
2.7
作者:
Charoenchaikorn, Kesinee;Yokomizo, Tomomasa;Yamashiro, Takashi
通讯作者:
Yamashiro, Takashi
影响因子:
4
作者:
Yamamoto S;Kurosaka H;Miura J;Aoyama G;Sarper SE;Oka A;Inubushi T;Nakatsugawa K;Usami Y;Toyosawa S;Yamashiro T
通讯作者:
Yamashiro T
DOI:
10.1016/j.jgg.2016.04.008
发表时间:
2016-05-20
期刊:
Journal of genetics and genomics = Yi chuan xue bao
影响因子:
--
作者:
Haeussler M;Concordet JP
通讯作者:
Concordet JP