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{"title":"Epithelium is required for maintaining FGFR-2 expression levels in facial mesenchyme of the developing chick embryo","authors":"Elizabeth Matovinovic, Joy M. Richman","doi":"10.1002/(SICI)1097-0177(199712)210:4<407::AID-AJA5>3.0.CO;2-K","DOIUrl":null,"url":null,"abstract":"<p>In the developing chick embryo, fibroblast growth factor-2 (FGFR-2) expression patterns correlate with outgrowth of facial prominences. Frontonasal mass prominences that form the pre-nasal cartilage and upper beak express high levels of FGFR-2 receptor, whereas maxillary prominences that form the flattened corners of the beak and palatal shelves express low FGFR-2 transcript levels. Facial epithelium is an abundant source of FGFs and is required to support outgrowth of mesenchymal tissue, including cartilage rod formation. Because FGFR-2 is highly expressed in regions of facial outgrowth and because epithelium is required for outgrowth of facial prominences, epithelium could be required to maintain FGFR-2 transcripts in facial mesenchyme. To test this hypothesis, we removed epithelium to inhibit outgrowth of regions of the embryonic face, grafted frontonasal mass and maxillary prominences into a host limb bud, and then examined changes in FGFR-2 expression usingin situ hybridization. We also hybridized adjacent sections with collagen II probe to identify regions undergoing chondrogenesis. Our results indicate that removal of epithelium from frontonasal mass led to a decrease in FGFR-2 and collagen II expression 24 hr after grafting to host and that neither FGFR-2 nor collagen II expression increased to expected levels at 48 hr. These results suggest that there are signals in the epithelium required for increasing FGFR-2 and collagen II gene transcription, and the expression of these genes are linked to outgrowth of facial prominences. <i>Dev. Dyn. 1997;210: 407–416.</i> © 1997 Wiley-Liss, Inc.</p>","PeriodicalId":11247,"journal":{"name":"Developmental Dynamics","volume":"210 4","pages":"407-416"},"PeriodicalIF":1.5000,"publicationDate":"1998-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://anatomypubs.onlinelibrary.wiley.com/doi/epdf/10.1002/%28SICI%291097-0177%28199712%29210%3A4%3C407%3A%3AAID-AJA5%3E3.0.CO%3B2-K","citationCount":"26","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental Dynamics","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/%28SICI%291097-0177%28199712%29210%3A4%3C407%3A%3AAID-AJA5%3E3.0.CO%3B2-K","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ANATOMY & MORPHOLOGY","Score":null,"Total":0}
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Abstract
In the developing chick embryo, fibroblast growth factor-2 (FGFR-2) expression patterns correlate with outgrowth of facial prominences. Frontonasal mass prominences that form the pre-nasal cartilage and upper beak express high levels of FGFR-2 receptor, whereas maxillary prominences that form the flattened corners of the beak and palatal shelves express low FGFR-2 transcript levels. Facial epithelium is an abundant source of FGFs and is required to support outgrowth of mesenchymal tissue, including cartilage rod formation. Because FGFR-2 is highly expressed in regions of facial outgrowth and because epithelium is required for outgrowth of facial prominences, epithelium could be required to maintain FGFR-2 transcripts in facial mesenchyme. To test this hypothesis, we removed epithelium to inhibit outgrowth of regions of the embryonic face, grafted frontonasal mass and maxillary prominences into a host limb bud, and then examined changes in FGFR-2 expression usingin situ hybridization. We also hybridized adjacent sections with collagen II probe to identify regions undergoing chondrogenesis. Our results indicate that removal of epithelium from frontonasal mass led to a decrease in FGFR-2 and collagen II expression 24 hr after grafting to host and that neither FGFR-2 nor collagen II expression increased to expected levels at 48 hr. These results suggest that there are signals in the epithelium required for increasing FGFR-2 and collagen II gene transcription, and the expression of these genes are linked to outgrowth of facial prominences. Dev. Dyn. 1997;210: 407–416. © 1997 Wiley-Liss, Inc.
在发育中的鸡胚面间质中,维持FGFR-2的表达水平需要上皮
在发育中的鸡胚中,成纤维细胞生长因子-2 (FGFR-2)的表达模式与面部隆起的生长相关。形成鼻前软骨和上喙的额鼻肿块突起表达高水平的FGFR-2受体,而形成喙的扁平角和腭架的上颌突起表达低水平的FGFR-2转录物。面部上皮是FGFs的丰富来源,需要支持间充质组织的生长,包括软骨棒的形成。由于FGFR-2在面部生长区域高表达,并且面部突出的生长需要上皮,因此可能需要上皮来维持面部间质中的FGFR-2转录本。为了验证这一假设,我们移除上皮以抑制胚胎面部区域的生长,将额鼻肿块和上颌突起移植到宿主肢体芽中,然后使用原位杂交检测FGFR-2表达的变化。我们还用胶原II探针对相邻切片进行杂交,以确定发生软骨形成的区域。我们的研究结果表明,额鼻肿块的上皮切除导致FGFR-2和II型胶原蛋白表达在移植到宿主24小时后下降,并且在48小时时FGFR-2和II型胶原蛋白表达均未增加到预期水平。这些结果表明,在上皮中存在增加FGFR-2和胶原II基因转录所需的信号,这些基因的表达与面部突出的生长有关。开发与应用。1997;21:407-416。©1997 Wiley-Liss, Inc
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