The timing of the earliest motor innervation to the hind limb bud in theXenopus tadpole

1974 ◽  
Vol 67 (3) ◽  
pp. 527-530 ◽  
Author(s):  
Alan H. Lamb
Keyword(s):  
Limb Bud ◽  
Development ◽  
1981 ◽  
Vol 65 (1) ◽  
pp. 149-163
Author(s):  
Alan H. Lamb

Bilateral innervation of a single hindlimb bud was induced by amputating the other limb bud and disrupting the barriers between the two sides. Though the routes of the crossed nerves were necessarily abnormal, the motor projections that developed subsequently were normal as determined by horseradish peroxidase tracing. The limb therefore appears to be innervated selectively, each region being invaded and/or synapsed with only by motoneurones at particular locations. The numbers of motoneurones surviving after metamorphosis were almost normal on both sides provided the operation was done before motor invasion of the limb bud begins. From this it is argued that the axons were probably guided actively to their correct destinations. Without such guidance, axons would probably not have been able to find their correct termination sites and motoneurone survival would therefore have been depressed. The normal motoneurone numbers also imply that the single limb was supporting twice its usual quota of motoneurones. The hypothesis that motoneurones compete in the limb for survival is therefore not supported.


Development ◽  
1996 ◽  
Vol 122 (5) ◽  
pp. 1449-1466 ◽  
Author(s):  
C.E. Nelson ◽  
B.A. Morgan ◽  
A.C. Burke ◽  
E. Laufer ◽  
E. DiMambro ◽  
...  

The vertebrate Hox genes have been shown to be important for patterning the primary and secondary axes of the developing vertebrate embryo. The function of these genes along the primary axis of the embryo has been generally interpreted in the context of positional specification and homeotic transformation of axial structures. The way in which these genes are expressed and function during the development of the secondary axes, particularly the limb, is less clear. In order to provide a reference for understanding the role of the Hox genes in limb patterning, we isolated clones of 23 Hox genes expressed during limb development, characterized their expression patterns and analyzed their regulation by the signalling centers which pattern the limb. The expression patterns of the Abd-B-related Hoxa and Hoxd genes have previously been partially characterized; however, our study reveals that these genes are expressed in patterns more dynamic and complex than generally appreciated, only transiently approximating simple, concentric, nested domains. Detailed analysis of these patterns suggests that the expression of each of the Hoxa and Hoxd genes is regulated in up to three independent phases. Each of these phases appears to be associated with the specification and patterning of one of the proximodistal segments of the limb (upper arm, lower arm and hand). Interestingly, in the last of these phases, the expression of the Hoxd genes violates the general rule of spatial and temporal colinearity of Hox gene expression with gene order along the chromosome. In contrast to the Abd-B-related Hoxa and Hoxd genes, which are expressed in both the fore and hind limbs, different sets of Hoxc genes are expressed in the two limbs. There is a correlation between the relative position of these genes along the chromosome and the axial level of the limb bud in which they are expressed. The more 3′ genes are expressed in the fore limb bud while the 5′ genes are expressed in the hind limb bud; intermediate genes are transcribed in both limbs. However, there is no clear correlation between the relative position of the genes along the chromosome and their expression domains within the limb. With the exception of Hoxc-11, which is transcribed in a posterior portion of the hind limb, Hoxc gene expression is restricted to the anterior/proximal portion of the limb bud. Importantly, comparison of the distributions of Hoxc-6 RNA and protein products reveals posttranscriptional regulation of this gene, suggesting that caution must be exercised in interpreting the functional significance of the RNA distribution of any of the vertebrate Hox genes. To understand the genesis of the complex patterns of Hox gene expression in the limb bud, we examined the propagation of Hox gene expression relative to cell proliferation. We find that shifts in Hox gene expression cannot be attributed to passive expansion due to cell proliferation. Rather, phase-specific Hox gene expression patterns appear to result from a context-dependent response of the limb mesoderm to Sonic hedgehog. Sonic hedgehog (the patterning signal from the Zone of Polarizing Activity) is known to be able to activate Hoxd gene expression in the limb. Although we find that Sonic hedgehog is capable of initiating and polarizing Hoxd gene expression during both of the latter two phases of Hox gene expression, the specific patterns induced are not determined by the signal, but depend upon the temporal context of the mesoderm receiving the signal. Misexpression of Sonic hedgehog also reveals that Hoxb-9, which is normally excluded from the posterior mesenchyme of the leg, is negatively regulated by Sonic hedgehog and that Hoxc-11, which is expressed in the posterior portion of the leg, is not affected by Sonic hedgehog and hence is not required to pattern the skeletal elements of the lower leg.


Development ◽  
1973 ◽  
Vol 29 (1) ◽  
pp. 221-237
Author(s):  
J. Geraudie ◽  
Y. François

The first stages of genesis of the pelvic fin Anlage in the Trout (Salmo fario and S. gairdneri). I. Anatomical study The Anlage of the pelvic fins appears in Salmo 2 weeks after the fecundation day, at the level of the somites 23–26. The mesoderm has a double origin and seems to differ in this regard from the hind limb of most of the amniotes. The ‘initial mesenchyme’ comes from the local proliferation of the somatopleura. It will give essentially the skeletal components of dermal origin (actinotrichia and lepidotrichia). The ‘secondary mesenchyme’ is obtained by the dispersion of four ventral somitic processes that have reached and entered the initial mesenchyme blastema. The secondary mesenchyme will probably give the muscles and also the endoskeleton of the fin. The origin of the girdle is not clear. When the setting of the initial mesenchyme begins the epithelium that covers the embryo is already differentiated in an epiderm with numerous mucous cells resting on a visible basement membrane. At the apex of the pelvic bud, a localized and transitory thickening of the epiderm is produced by the increase in the height of the basal stratum. We call this structure by the name of ‘pseudo apical cap’ to stress the fact that it must be distinguished from the ‘apical cap’ described for the limb bud of amniotes. So, the morphogenesis of the pelvic fins of Salmo shows some important particularities in the epiderm as well as in the mesoderm.


Development ◽  
1973 ◽  
Vol 30 (3) ◽  
pp. 673-679
Author(s):  
P. V. Thorogood

Myotubes are present in the developing hind limb of the embryonic chick at 5 days. An immunofluorescence technique was used to detect actomyosin within the myotubes. The earliest detectable appearance of this muscle protein was at six days of development, at sites located peripherally beneath the flattened dorsal and ventral surface of the limb. These dorsal and ventral loci are interpreted as representing the primordial extensor and flexor muscles. At the ultrastructural level the cytoplasm of the myotubes contains fibrillar components which are apparently aggregating to form myofibrils. A rudimentary banding pattern can be distinguished.


Development ◽  
1975 ◽  
Vol 33 (3) ◽  
pp. 581-606
Author(s):  
P. V. Thorogood ◽  
J. R. Hinchliffe

An analysis has been made of the pre-cartilaginous condensation stage in the development of the femur and tibia/fibula skeletal blastemata of the embryonic chick hind limb. Light microscopy serial sections were used to ‘map’ the mesenchymal cell condensations of both myogenic and chondrogenic anlagen in the limb-bud from stages 22 to 26 (Hamburger & Hamilton, 1951). Cell counts reveal that an increase in mesenchymal cell number per unit area occurs in the central chondrogenic locus at stage 24 (4½ days) prior to matrix formation. Electron microscopy, using a simultaneous double fixation with osmium and glutaraldehyde, reveals that the pre-chondrogenic cells are characterized by large areas of close surface contact between adjacent cells, as compared with the extensive intercellular spaces associated with undifferentiated mesenchymal cells. The results are discussed and related to other investigations of in vivo chondrogenesis and to analyses of cellular events during in vitro chondrogenesis. These observations are consistent with the theory that condensations are formed by a process of aggregation rather than by localized increased mitosis.


Development ◽  
1984 ◽  
Vol 83 (1) ◽  
pp. 213-223
Author(s):  
N. G. Laing

Chick embryo wing buds were rotated close to the lateral edge of the somites at stage 19, prior to limb innervation. Despite the abnormal orientation of the resulting limb, the motor pools to biceps and triceps were largely normal, as judged by electrical stimulation and horseradish peroxidase labelling just prior to hatching. The only abnormalities were a few caudal motoneurons innervating biceps and a few rostral motoneurons innervating triceps. This distribution is similar to that seen normally in young embryos before the completion of motoneuron death and it is suggested that the rotation may be keeping alive motoneurons which otherwise would die. The morphology of the brachial plexus supplying rotated wings was abnormal. It is concluded that axons growing into the limb bud from the spinal cord can compensate for reversal of both the limb axes and selectively innervate appropriate muscles. The result is consistent with others in which proximal reversal of one limb axis alone produced normal innervation.


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