RESUMEN
In the vertebrate embryo, neural cell types are organized spatially along the dorsoventral axis of the neural tube and differ by expression of cell-intrinsic determinants and by their adhesive and locomotory properties. Thus, dorsally, neural crest cells (NCC) show a strong propensity to disperse and migrate, whereas cells situated ventrally are highly cohesive and poorly motile. Members of the bone morphogenetic proteins have been shown to exert a dual role in the specification of dorsal neuroepithelial cells and in the dispersion of NCCs. To test whether Sonic hedgehog (Shh), another signaling molecule involved in the patterning of the ventral neural tube, might also contribute to the control of the adhesive and migratory potential of neuroepithelial cells, we analyzed the effect of ectopic Shh on NCC dispersion from neural tube explants cultured in vitro. The addition of Shh to the migration substrate of NCC caused inhibition of their dispersion. The effect of Shh on cell migration was reversible and was not accounted for by alterations of the specification, delamination, proliferation, and survival of NCCs but could be essentially attributed to a decreased cell-substrate adhesion mediated by integrins. In addition, Shh activity on cell migration was mediated by a specific N-terminal region of the molecule and was independent from the signaling cascade elicited by the Patched-Smoothened receptor and involving the Gli transcription factors. Our study therefore reveals an unanticipated role for Shh in regulating adhesion and migration of neuroepithelial cells that is discernable from its inductive, mitogenic, and trophic functions.
Asunto(s)
Cresta Neural/citología , Proteínas Oncogénicas/fisiología , Receptores de Superficie Celular/fisiología , Receptores Acoplados a Proteínas G , Transactivadores/fisiología , Factores de Transcripción/fisiología , Animales , Proteínas Morfogenéticas Óseas/fisiología , Adhesión Celular , Movimiento Celular , Embrión de Pollo , Proteínas Hedgehog , Humanos , Integrinas/fisiología , Codorniz , Receptor Smoothened , Proteína con Dedos de Zinc GLI1RESUMEN
BEN/SC1/DM-GRASP is a cell adhesion molecule belonging to the Ig superfamily that is transiently expressed during avian embryogenesis in a variety of cell types, including the motoneurons of the spinal cord. We have investigated the pattern of BEN expression during neuromuscular development of the chick. We show that both motoneurons and their target myoblasts express BEN during early embryonic development and that the protein becomes restricted at neuromuscular contacts as soon as postsynaptic acetylcholine receptor clusters are observed in muscle fibers. Muscle cells grown in vitro express and maintain BEN expression even when they fuse and give rise to mature myotubes. When embryos are deprived of innervation by neural tube ablation, BEN expression is observed in muscle fibers, whereas, in control, the protein is already restricted at neuromuscular synaptic sites. These results demonstrate that all myogenic cells intrinsically express BEN and maintain the protein in the absence of innervation. Conversely, when neurons are added to myogenic cultures, BEN is rapidly downregulated in muscle cells, demonstrating that innervation controls the restricted pattern of BEN expression seen in innervated muscles. After nerve section in postnatal muscles, BEN protein becomes again widely spread over muscle fibers. When denervated muscles are allowed to be reinnervated, the protein is reexpressed in regenerating motor axons, and reinnervation of synaptic sites leads to the concentration of BEN at neuromuscular junctions. Our results suggest that BEN cell adhesion molecule acts both in the formation of neuromuscular contacts during development and in the events leading to muscle reinnervation.
Asunto(s)
Molécula de Adhesión Celular del Leucocito Activado/biosíntesis , Desarrollo de Músculos , Músculo Esquelético/crecimiento & desarrollo , Músculo Esquelético/inervación , Moléculas de Adhesión de Célula Nerviosa/biosíntesis , Animales , Células Cultivadas , Embrión de Pollo , Pollos , Desnervación , Immunoblotting , Inmunohistoquímica , Hibridación in Situ , Fibras Musculares Esqueléticas/metabolismo , Músculo Esquelético/metabolismo , Unión Neuromuscular/fisiologíaRESUMEN
Myogenic Regulatory Factors (MRFs) are a family of transcription factors whose expression in a cell reflects the commitment of this cell to a myogenic fate before any cytological sign of muscle differentiation is detectable. Myogenic cells in limb skeletal muscles originate from the lateral half of the somites. Cells that migrate away from the lateral part of the somites to the limb bud do not initially express any member of the MRF family. Expression of MRFs in the muscle precursor cells starts after the migration process is completed. The extracellular signals involved in activating the myogenic programme in muscle precursor cells in the limb in vivo are not known. We wished to investigate whether Sonic Hedgehog (SHH) expressed in the posterior part of the limb bud could be involved in differentiation of the muscle precursor cells in the limb. We found that retrovirally overexpressed SHH in the limb bud induced the extension of the expression domain of the Pax-3 gene, then that of the MyoD gene and finally that of the myosin protein. This led to an hypertrophy of the muscles in vivo. Addition of SHH to primary cultures of myoblasts resulted in an increase in the proportion of myoblasts that incorporate bromodeoxyuridine, resulting in an increase of myotube number. These data show that SHH is able to activate myogenesis in vivo and in vitro in already committed myoblasts and suggest that the stimulation of the myogenic programme by SHH involves activation of cell proliferation.
Asunto(s)
Esbozos de los Miembros/embriología , Músculo Esquelético/citología , Músculo Esquelético/embriología , Proteínas/fisiología , Transactivadores , Factores de Transcripción , Animales , División Celular , Células Cultivadas , Embrión de Pollo , Proteínas de Unión al ADN/genética , Fibroblastos/trasplante , Regulación del Desarrollo de la Expresión Génica , Proteínas Hedgehog , Proteínas de la Membrana/genética , Mesodermo , Músculo Esquelético/química , Proteína MioD/genética , Miosinas/genética , Factor de Transcripción PAX3 , Factores de Transcripción Paired Box , Receptores Patched , Proteínas/genética , ARN Mensajero/análisis , Receptores de Superficie Celular , Células MadreRESUMEN
This study investigated possible interactions between motoneurons and somitic-derived muscle cells in the formation of neuromuscular synapses in the myotome. The peculiarities of the neuromuscular synaptic pattern in chick and mouse embryos provided a model for studying the achievement of synaptogenesis between chick motoneurons and mouse muscle cells. In chick embryo, initial AChR clustering occurs well before innervation of the myotome, whereas in mouse embryo nerve axons invade the myotome extensively before the appearance of AChR clusters. Our approach was to replace somites from a chick host embryo with those derived from mouse donor embryos. We show that muscle cells from mouse myotome can differentiate in the chick embryo environment and form neuromuscular contacts with chick motor axons. Host axons invaded in ovo differentiating mouse myotome at a time when they had not yet reached the host myotome. This particular ingrowth of motor nerves was attributable to the mouse transplant since use of a quail somite did not produce the same effect as the mouse somite, which suggests that developing mouse muscles specifically modify the time course of chick axogenesis. The synaptic areas formed between chick motor axons and mouse myotubes developed according to the mouse pattern. Both the timing of their appearance and their morphology correlated perfectly with events in mouse synaptogenesis. These results indicate the important role played by postsynaptic membrane in controlling the first steps of AChR formation.