Cues from neuroepithelium and surface ectoderm maintain neural crest-free regions within cranial mesenchyme of the developing chick.
نویسندگان
چکیده
Within the developing vertebrate head, neural crest cells (NCCs) migrate from the dorsal surface of the hindbrain into the mesenchyme adjacent to rhombomeres (r)1 plus r2, r4 and r6 in three segregated streams. NCCs do not enter the intervening mesenchyme adjacent to r3 or r5, suggesting that these regions contain a NCC-repulsive activity. We have used surgical manipulations in the chick to demonstrate that r3 neuroepithelium and its overlying surface ectoderm independently help maintain the NCC-free zone within r3 mesenchyme. In the absence of r3, subpopulations of NCCs enter r3 mesenchyme in a dorsolateral stream and an ectopic cranial nerve forms between the trigeminal and facial ganglia. The NCC-repulsive activity dissipates/degrades within 5-10 hours of r3 removal. Initially, r4 NCCs more readily enter the altered mesenchyme than r2 NCCs, irrespective of their maturational stage. Following surface ectoderm removal, mainly r4 NCCs enter r3 mesenchyme within 5 hours, but after 20 hours the proportions of r2 NCCs and r4 NCCs ectopically within r3 mesenchyme appear similar.
منابع مشابه
Roles of erbB4, rhombomere-specific, and rhombomere-independent cues in maintaining neural crest-free zones in the embryonic head.
Within the developing vertebrate head, the migration of neural tube-derived neural crest cells (NCCs) through the cranial mesenchyme is patterned into three streams, with mesenchyme adjacent to rhombomeres (r)3 and r5 maintained NCC-free. The receptor tyrosine kinase erbB4 is expressed within r3 and r5 and is required to maintain the r3-adjacent NCC-free zone in mouse embryos. In this study, we...
متن کاملINTRODUCTION Within the developing vertebrate head, the organisation of skeletal structures and peripheral nerves depends on the orchestrated migration of pluripotent cranial neural crest cells
Within the developing vertebrate head, the organisation of skeletal structures and peripheral nerves depends on the orchestrated migration of pluripotent cranial neural crest cells (NCCs) through the cranial mesenchyme (Bronner-Fraser, 1995; Le Douarin, 1982). Cranial NCCs are generated throughout the dorsal hindbrain (Sechrist et al., 1993) but their emigration into the adjacent mesenchyme is ...
متن کاملCongenital eye malformations associated with extensive periocular neural crest apoptosis after influenza B virus infection during early embryogenesis
PURPOSE Congenital eye malformations are a leading cause of blindness in children. Influenza virus infections prevail worldwide and have been implicated in congenital defects. Infections acquired during gestation may disrupt eye morphogenesis. We investigated the effects of influenza B virus infection on eye malformations during early embryogenesis. METHODS Chick embryos were exposed to influ...
متن کاملUpdate on Anterior Segment Development with Emphasis on Genetics and Correlation with Pathogenesis of Developmental & Primary Open Angle Glaucoma
There are 3 elements which contribute to the development of the human eye in the primitive embryo: the surface ectoderm, the neuroectoderm, and the neural crest which has been recognized as a potential source of mesenchymal tissue. The meso-dermal contribution is limited to the formation of extra ocular muscles and blood vessels endothelium [1]. The vertebrate neural crest not only gives rise t...
متن کاملThe tight junction protein claudin-1 influences cranial neural crest cell emigration
The neural crest is a population of migratory cells that follows specific pathways during development, eventually differentiating to form parts of the face, heart, and peripheral nervous system, the latter of which includes contributions from placodal cells derived from the ectoderm. Stationary, premigratory neural crest cells acquire the capacity to migrate by undergoing an epithelial-to-mesen...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Development
دوره 129 5 شماره
صفحات -
تاریخ انتشار 2002