Literature DB >> 22945385

Does the cranial mesenchyme contribute to neural fold elevation during neurulation?

Irene E Zohn1, Anjali A Sarkar.   

Abstract

The central nervous system is derived from the neural plate, which undergoes a series of complex morphogenetic events resulting in formation of the neural tube in a process known as neurulation. The cellular behaviors driving neurulation in the cranial region involve forces generated by the neural tissue itself as well as the surrounding epithelium and mesenchyme. Of interest, the cranial mesenchyme underlying the neural plate undergoes stereotypical rearrangements hypothesized to drive elevation of the neural folds. As the neural folds rise, the hyaluronate-rich extracellular matrix greatly expands resulting in increased space between individual cranial mesenchyme cells. Based on inhibitor studies, expansion of the extracellular matrix has been implicated in driving neural fold elevation; however, because the surrounding neural and epidermal ectoderm were also affected by inhibitor exposure, these studies are inconclusive. Similarly, treatment of neurulating embryos with teratogenic doses of retinoic acid results in altered organization of the cranial mesenchyme, but alterations in surrounding tissues are also observed. The strongest evidence for a critical role for the cranial mesenchyme in neural fold elevation comes from studies of genes expressed exclusively in the cranial mesenchyme that when mutated result in exencephaly associated with abnormal organization of the cranial mesenchyme. Twist is the best studied of these and is expressed in both the paraxial mesoderm and neural crest derived cranial mesenchyme. In this article, we review the evidence implicating the cranial mesenchyme in providing a driving force for neural fold elevation to evaluate whether there are sufficient data to support this hypothesis.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22945385      PMCID: PMC3473154          DOI: 10.1002/bdra.23073

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN: 1542-0752


  73 in total

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6.  Hyaluronan constitutively regulates ErbB2 phosphorylation and signaling complex formation in carcinoma cells.

Authors:  Shibnath Ghatak; Suniti Misra; Bryan P Toole
Journal:  J Biol Chem       Date:  2005-01-04       Impact factor: 5.157

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Authors:  Mi-Suk Kim; Hee-Jin Kwak; Ji-Woo Lee; Hea-Jin Kim; Myung-Jin Park; Jong-Bae Park; Kyung-Ho Choi; Heon Yoo; Sang-Hoon Shin; Woon-Seob Shin; Eun-Sook Song; Seung-Hoon Lee
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Review 2.  Insights into the Etiology of Mammalian Neural Tube Closure Defects from Developmental, Genetic and Evolutionary Studies.

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Review 3.  Neural tube closure: cellular, molecular and biomechanical mechanisms.

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