Muscle and tendon morphogenesis in the avian hind limb

Development ◽  
1998 ◽  
Vol 125 (20) ◽  
pp. 4019-4032 ◽  
Author(s):  
G. Kardon

The proper development of the musculoskeletal system in the tetrapod limb requires the coordinated development of muscle, tendon and cartilage. This paper examines the morphogenesis of muscle and tendon in the developing avian hind limb. Based on a developmental series of embryos labeled with myosin and tenascin antibodies in whole mount, an integrative description of the temporal sequence and spatial pattern of muscle and tendon morphogenesis and their relationship to cartilage throughout the chick hind limb is presented for the first time. Anatomically distinct muscles arise by the progressive segregation of muscle: differentiated myotubes first appear as a pair of dorsal and ventral muscle masses; these masses subdivide into dorsal and ventral thigh, shank and foot muscle masses; and finally these six masses segregate into individual muscles. From their initial appearance, most myotubes are precisely oriented and their pattern presages the pattern of future, individual muscles. Anatomically distinct tendons emerge from three tendon primordia associated with the major joints of the limb. Contrary to previous reports, comparison of muscle and tendon reveals that much of their morphogenesis is temporally and spatially closely associated. To test whether reciprocal muscle-tendon interactions are necessary for correct muscle-tendon patterning or whether morphogenesis of each of these tissues is autonomous, two sets of experiments were conducted: (1) tendon development was examined in muscleless limbs produced by coelomic grafting of early limb buds and (2) muscle development was analyzed in limbs where tendon had been surgically altered. These experiments demonstrate that in the avian hind limb the initial morphogenetic events, formation of tendon primordia and initial differentiation of myogenic precursors, occur autonomously with respect to one another. However, later morphogenetic events, such as subdivision of muscle masses and segregation of tendon primordia into individual tendons, do require to various degrees reciprocal interactions between muscle and tendon. The dependence of these later morphogenetic events on tissue interactions differs between different proximodistal regions of the limb.

1990 ◽  
Vol 68 (6) ◽  
pp. 1281-1287 ◽  
Author(s):  
Christine M. Dwyer ◽  
James Hanken

We examine limb skeletal variability in Plethodon neomexicanus, a geographically isolated species of plethodontid salamander endemic to the Jemez Mountains of New Mexico, U.S.A. Data are derived from a series of 25 specimens prepared as whole mounts stained for bone and cartilage. Only 25% of hind limbs display the derived hind limb phalangeal formula 1-2-3-3-1, once considered characteristic of this species; two hind limb and one forelimb phalangeal formulae are reported for the first time. In addition, there are six variant carpal and tarsal patterns as well as the two predominant, primitive mesopodial patterns that are typical of most other species of Plethodon as well as of many other plethodontid genera. Limb skeletal variability in P. neomexicanus is among the highest recorded for urodeles and may represent an ancient and widespread polymorphism in the genus Plethodon.


Author(s):  
Leilei Xu ◽  
Zhenhua Feng ◽  
Zhicheng Dai ◽  
Wayne Y. W. Lee ◽  
Zhichong Wu ◽  
...  

Previous studies have shown that LBX1 is associated with adolescent idiopathic scoliosis (AIS) in multiple populations. For the first time, rs1322330 located in the putative promoter region of LBX1 was found significantly associated with AIS in the Chinese population [p = 6.08 × 10–14, odds ratio (OR) = 1.42, 95% confidence interval of 1.03–1.55]. Moreover, the luciferase assay and electrophoretic mobility shift assay supported that the allele A of rs1322330 could down-regulate the expression of LBX1 in the paraspinal muscles of AIS. In addition, silencing LBX1 in the myosatellite cells resulted in significantly inhibited cell viability and myotube formation, which supported an essential role of LBX1 in muscle development of AIS. To summarize, rs1322330 may be a novel functional SNP regulating the expression of LBX1, which was involved in the etiology of AIS possibly via regulation of myogenesis in the paraspinal muscles.


Development ◽  
1980 ◽  
Vol 58 (1) ◽  
pp. 251-264
Author(s):  
Brian K. Hall

Mandibular processes from 9- to 13-day-old embryonic mice formed both bone and cartilage when grafted to the chorioallantoic membranes of host embryonic chicks. Isolated ectomesenchyme, taken from 9-day-old embryos did not form bone or cartilage, while older ectomesenchyme formed both. Recombination of the epithelial and ectomesenchymal components confirmed that the presence of the epithelium was a sufficient stimulus for the initiation of both chondro- and osteogenesis. Recombinations between components of mouse and chick mandibular processes showed that 9-day-old mouse ectomesenchyme could respond to chick epithelium but that, although older murine epithelia could initiate osteogenesis from the avian ectomesenchyme, epithelia from 9-day-old embryos could not. These results indicated that an epithelial-ectomesenchymal interaction was responsible for the initiation of both osteo- and chondrogenesis within the mandibular arch of the mouse; that the interaction began at 10 days of gestation; that the ectomesenchyme was capable of responding at 9 days, but that the epithelium did not acquire its ability to act on the ectomesenchyme until 10 days of gestation.


Author(s):  
J.L Hornick ◽  
A. Clinquart ◽  
C. Van Eenaeme ◽  
S. Gauthier ◽  
L. Istasse

Aside from its function of contraction, the muscle is also a pool of mobilisable protein which may be released or stored according to the needs of the animal. An approach of this aspect can be theorically studied by measure of arterio-venous differences of plasma metabolites from blood in the muscle mass. The aim of this experiment was to study uptake of α amino-nitrogen, glucose and urea across the hind-limb of bulls from a breed with large muscle development.Three bulls from the Belgian Blue breed-double muscled type-were used. They weighed about 300 kg when an ultrasonic flow probe (Transonic Systems, Inc.,Ithaca, NY) was implanted around the abdominal aorta, back to the renal vessels, in order to measure the blood flow in the hind-leg (Eisemann et al., 1987). After an one month recovery period, circumflex iliac artery and vein were implanted with catheters. During the periods of surgery, the bulls were offered hay only at a rate of three kg daily. Ten days after the second surgery, increasing amounts of concentrate were given with the hay so that the animals received one kg concentrate on day 1 (level 1), three kg concentrate on day 3 (level 3), five kg concentrate on day 5 (level 5).


Development ◽  
1989 ◽  
Vol 107 (4) ◽  
pp. 819-824 ◽  
Author(s):  
P.J. Barton ◽  
A.J. Harris ◽  
M.E. Buckingham

We have investigated the accumulation of mRNA transcripts of the atrial (or embryonic) myosin light chain MLC1A (MLC1emb), and the two adult fast muscle myosin light chains (MLC1F and MLC3F) during fetal skeletal muscle development in the mouse. In 15-day fetal muscle, MLC1A is the predominant mRNA detectable, by 18 days MLC1F has become the major transcript and MLC3F mRNA is detectable for the first time. By 12 days after birth, MLC1A transcripts are undetectable and MLC1F and MLC3F are similar in abundance. In fetuses treated with beta-bungarotoxin and which therefore develop in the absence of functional nerve, MLC1A and MLC1F undergo normal transitions but MLC3F mRNA accumulation is significantly retarded. This demonstrates that these myosin light chain mRNAs accumulate with differing kinetics, and that MLC3F mRNA accumulation is nerve-dependent during fetal development. The results are discussed in terms of secondary muscle fibre formation, and in relation to the independent regulation of MLC1F and MLC3F mRNAs which are transcribed from the same gene.


2003 ◽  
Vol 23 (3) ◽  
pp. 364-370 ◽  
Author(s):  
Cristina Sánchez–Fernández ◽  
Carmen González ◽  
Linda D. Mercer ◽  
Philip M. Beart ◽  
Mariano Ruiz–Gayo ◽  
...  

The authors report that cholecystokinin (CCK), via its subtype 2 receptor (CCK2R) located presynaptically on cerebral arteries, mediates the release of nitric oxide (NO), which induces vasodilatation. Whereas CCK octapeptide and its fragment CCK tetrapeptide (CCK-4) lack a direct effect on the smooth muscle of pial vessels, the authors showed that both CCK peptides modulate the neurogenic responses in bovine cerebral arteries. The neurogenic vasodilatation induced by CCK-4 was blocked by the CCK2R antagonist, L-365,260, and antagonized by neuronal NO synthase (nNOS) inhibitors, but was independent of the endothelium. In whole-mount arteries, CCK2Rs were detected in nerve fibers and colocalized with nNOS and synaptophysin. The findings provide, for the first time, a neural mechanism by which CCK may increase cerebral blood flow.


Author(s):  
Anna Svensson ◽  
Sven Tågerud

AbstractGalectin-1 is a soluble carbohydrate-binding protein with a particularly high expression in skeletal muscle. Galectin-1 has been implicated in skeletal muscle development and in adult muscle regeneration, but also in the degeneration of neuronal processes and/or in peripheral nerve regeneration. Exogenously supplied oxidized galectin-1, which lacks carbohydrate-binding properties, has been shown to promote neurite outgrowth after sciatic nerve sectioning. In this study, we compared the expression of galectin-1 mRNA and immunoreactivity in innervated and denervated mouse and rat hind-limb and hemidiaphragm muscles. The results show that galectin-1 mRNA expression and immunoreactivity are up-regulated following denervation. The galectin-1 mRNA is expressed in the extrasynaptic and perisynaptic regions of the muscle, and its immunoreactivity can be detected in both regions by Western blot analysis. The results are compatible with a role for galectin-1 in facilitating reinnervation of denervated skeletal muscle.


1967 ◽  
Vol 32 (1) ◽  
pp. 1-10 ◽  
Author(s):  
Woutera van Iterson ◽  
Judith F. M. Hoeniger ◽  
Eva Nijman van Zanten

A study of the anchorage of the flagella in swarmers of Proteus mirabilis led to the incidental observation of microtubules. These microtubules were found in thin sections and in whole mount preparations of cells from which most of the content had been released by osmotic shock before staining negatively with potassium phosphotungstate (PTA). The microtubules are in negatively stained preparations about 200 A wide, i.e. somewhat thicker than the flagella (approximately 130 A). They are thus somewhat thinner than most microtubules recorded for other cells. They are referred to as microtubules because of their smooth cylindrical wall, or cortex, surrounding a hollow core which is readily filled with PTA when stained negatively. Since this is probably the first time that such a structure is described inside a bacterium, we do not know for certain whether it represents a normal cell constituent or an abnormality, for instance of the type of "polysheaths" (16).


Sign in / Sign up

Export Citation Format

Share Document