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At least 19 recordsLinked to original sources
PubMed1989

The formation of leg or wing specific structures by leg bud cells grafted to the wing bud is influenced by proximity to the apical ridge.

When quail or chick leg bud mesoderm was grafted to a chick wing bud, toes developed from grafts placed in direct contact with the wing apical ridge. The toes were primarily derived from quail leg cells, with variable participation of host wing cells. Donor cells also integrated into wing-specific structures, such as cartilage of the wing digits and the surrounding connective tissues. In addition to forming toes, the grafted leg mesoderm expressed its leg origin by enlarging skeletal elements in the host wing. In all cases, enlargements were derived of both quail donor and chick host cells, and were not the result of the addition of mass to the host bud. Grafts placed further than 162 microns from the ridge formed neither toes nor enlargements; rather, they integrated into wing-specific structures. Under the influence of the apical ridge, the grafted leg mesoderm cells are able to maintain their leg character and to form toes and skeletal enlargements. Grafts outside the range of ridge influence (162 microns) are affected by their surroundings to integrate into wing-specific structures. The formation of leg-specific structures by leg bud mesoderm grafted to the wing bud has been used to support the principle of nonequivalence, which states that, because of their different developmental histories, wing and leg cells are restricted to form structures specific for their respective limbs. However, we have shown that leg cells can form wing-specific structures, and therefore limb cells are not restricted in their development.

Animals↗
PubMed1992

Effect of wing scalloping mutations on cut expression and sense organ differentiation in the Drosophila wing margin.

A number of wing scalloping mutations have been examined to determine their effects on the mutant phenotype of cut mutations and on the expression of the Cut protein. The mutations fall into two broad classes, those which interact synergistically with weak cut wing mutations to produce a more extreme wing phenotype than either mutation alone and those that have a simple additive effect with weak cut wing mutations. The synergistically interacting mutations are alleles of the Notch, Serrate and scalloped genes. These mutations affect development of the wing margin in a manner similar to the cut wing mutations. The mutations inactivate the cut transcriptional enhancer for the wing margin mechanoreceptors and noninnervated bristles and prevent differentiation of the organs. Surprisingly, reduction of Notch activity in the wing margin does not have the effect of converting epidermal cells to a neural fate as it does in other tissues of ectodermal origin. Rather, it prevents the differentiation of the wing margin mechanoreceptors and noninnervated bristles.

Alleles↗
PubMed1990

The orientation of the wing mesenchyme influences the direction of the migration of myoblasts in the avian embryonic wing bud.

In order to analyze the influence of the orientation of the wing bud mesenchyme on the proximodistal direction of the migration of myoblasts in the avian embryonic wing bud, blocks of wing-bud mesenchyme were cut out and rotated around a dorso-palmar axis through 90 degrees or 180 degrees. Tissues originating from the quail wing bud and containing myoblasts were grafted into the space between the wing mesenchyme and the rotated blocks of mesenchyme proximal to the latter. In all experiments the donor-embryos were older than the acceptor-embryos. From HH stage 24 on, the rotation of the block of mesenchyme inhibited the migration of the myoblasts in a distal direction. We therefore propose that the orientation of the wing bud mesenchyme has an influence on the migratory behavior of myoblasts. This influence could provide "directional information" for the migrating myoblasts, allowing the migration of myoblasts in a distal direction only.

Animals↗
PubMed1992

Evaluation of ground ambulance, rotor-wing, and fixed-wing aircraft services.

It is hoped that this article has offered insightful suggestions and criteria in choosing the most appropriate method to transport patients. Ground ambulances, rotor-wing, and fixed-wing aircraft each have advantages and disadvantages in particular circumstances. The advantages and disadvantages of any mode of transport must be considered to best meet the needs of the patient. In the twentieth century alone, great strides have been made in the field of emergency stabilization and transport. An efficient, well-trained ground ambulance program remains the backbone of prehospital and interhospital transport systems. Helicopters and fixed-wing transports must be integrated into the EMS system. One advantage of the helicopter and fixed-wing aircraft is rapid travel times when time is critical. As Hicks et al said, "early resuscitation and timely transfer of selected patients are critical factors in reducing morbidity and mortality." The future holds many possibilities for enhanced patient transport. Hospitals may be able to use tilt-rotor, vertical landing, fixed-wing aircraft to combine the advantages of helicopter and fixed-wing aircraft. After all, our primary goal is to get the right patient, with the right personnel, to the right place in the right amount of time.

Aircraft↗
PubMed1992

The development of normal and ectopic sensilla in the wings of hairy and Hairy wing mutants of Drosophila.

We have utilized enhancer trap markers to follow the development of ectopic sensillar precursors in the wings of Drosophila induced by the mutations hairy and Hairy wing. Normal sensilla are still present in these mutations, and can be distinguished from ectopic sensilla based upon both the position and the timing of their development. This correlates well with the development of ectopic achaete expression in these mutations: such staining is detected only after the appearance of normal staining. Thus, neither mutation appears to alter the specification of proneural clusters in the wing, as identified with anti-achaete, or the specification of sensillar precursors within these clusters. Rather, both act to induce the formation of a temporally and spatially distinct phase of sensillar development.

Animals↗
PubMed1990

The behaviour of cells from the distal tips of quail wing buds when grafted back into chick wings after micromass culture.

In high density culture, cells from distal tips of developing limb buds differentiate into a continuous cartilage sheet, rich in type II collagen. When grafted back into limb buds, cells cultured for a short time differentiate into cartilage and a wide range of other connective tissues, whereas cells taken from older cultures give rise only to cartilage and perichondrium. Grafts placed distally give rise to more cell types than grafts placed proximally. The results strongly suggest that chondrogenesis in culture is the result of removing the signals that pattern differentiation within the limb bud.

Animals↗
PubMed1985

Myogenic differentiation in early chick wing mesenchyme in the absence of the brachial somites.

A controversy exists in the literature over the ability of wing mesenchyme of somatopleural origin to form skeletal muscle. Experimental approaches used in such studies leave open the possibility of postoperative accessibility of the experimental wings to somitic cell invasion. In the present study wing somatopleural tissue was isolated from HH stage-12 to -21 chick embryos and grown either in organ culture (OC) or on the chorioallantoic membrane (CAM) of host chicks, conditions under which postoperative entry of somitic cells is impossible. In the presence of axial and somitic tissues of the brachial region, the wing territories from all four stages underwent comparable growth and tissue differentiation. However, isolated wing regions showed a stage-dependency in the differentiation of skeletal muscle but not of other limb tissues. The incidence and amount of skeletal muscle was markedly reduced in HH stage-12 and -15 isolated wing regions while myogenesis in HH stage-18 and -21 wing buds was not affected by the absence of the somitic tissues. These results are consistent with reported stages of somitic cell migration into wings with the exception of HH stage-12 explants which should have been muscleless if somitic cells are the sole source of wing myofibres. The possibility that somitic cells had been included in these explants was investigated by testing the myogenic potential of lateral plate tissue adjacent to the wing, altering the dissection procedure for isolating wing territories and using antibodies to skeletal muscle myosin and actin to detect myotubes. The results from this series of experiments illustrate the need for extraordinary care in the isolation of wing regions when investigating limb-somite relationships and suggest that the myogenic capacity attributed to wing somatopleural cells in the past can be accounted for by either postoperative entry of somitic cells into experimental wings or inadvertent inclusion of somitic cells in the primordia when dissected. Overall, the results show that somitic cells are the sole source of wing myofibres for, in their absence, somatopleural cells from all mesodermally-derived wing cell types except skeletal myofibres.

Animals↗
PubMed1990

Development of the embryonic chick wing bud from stage 24 to stage 32.

If a graft is placed in an early chick wing bud, the location of the graft after several days of further development cannot be predicted solely from the rate of proximal-distal outgrowth. The movement of the graft depends on the rate of outgrowth of the wing but also on morphogenetic tissue movements intrinsic to the wing and on accommodation to the growth and morphogenetic movements of the body of the embryo. Numerous experiments have been reported in which tissue grafted into ectopic sites in the wing causes abnormal wing development. These experiments have been discussed in terms of pattern formation or positional information. However, until the movement of wing tissue during normal development is understood, it cannot be known in what way the development of grafts placed in ectopic sites is abnormal. Previous experiments have demonstrated that carbon particles placed in the wing move in the same manner as grafts of wing mesenchyme, but the carbon particles do not affect normal wing development. Carbon particles were placed in the wing, dorsal to the base of the wing, and cranial and caudal to the wing, to plot the expected movement of a graft and to discover how this movement can be predicted from the tissue movements at the base of the wing. It is concluded that three tissue movements are responsible for the movement of a graft. These are outgrowth at a rate determined by the rate of cell division, formation of the shoulder through caudal movement of the tissues cranial to the wing, and ventral movement of prospective flank ventral to somite 19. These three tissue movements and their influence on normal wing development are discussed.

Animals↗
PubMed1992

Coordination of wingbeat and respiration in the Canada goose. I. Passive wing flapping.

The effects of passive wing flapping on respiratory pattern were examined in decerebrate Canada geese. The birds were suspended dorsally with two spine clamps while the extended wings were continuously moved up and down with a device designed to reproduce actual wing flapping. Passive wing motion entrained respiration over limited ranges by both increasing and decreasing the respiratory period relative to rest. All ratios of wingbeat frequency to respiratory frequency seen during free flight (Soc. Neurosci. Abstr. 15: 391, 1989) were produced during passive wing flapping. In addition, the phase relationship between wingbeat frequency and respiratory frequency, inspiration starting near the peak of wing upstroke, was similar to that seen during free flight and was unaffected by perturbations of the wing-flapping cycle. Removal of all afferent activity from the wings did not affect the ability of continuous passive wing movement to entrain respiration. However, feedback from the wings was required to produce rapid within-breath shifts in the respiratory period in response to single wing flaps. In conclusion, although feedback from the chest wall/lung may be more important in producing entrainment during the stable conditions of passive wing flapping, wing-related feedback may be critically involved in mediating the rapid adjustments in respiratory pattern required to maintain coordination between wing and respiratory movements during free flight.

Afferent Pathways↗
PubMed1991

Programmed cell death in the wing of Orgyia leucostigma (Lepidoptera: Lymantriidae).

Programmed cell death is an integral and ubiquitous phenomenon of development that is responsible for the reduction of wing size in female moths of Orgyia leucostigma (Lymantriidae). Throughout larval and pupal life, cells of the wing epithelium proliferate and interact to form normal imaginal discs and pupal wings in both sexes. But at the onset of adult development, most cells in female O. leucostigma wings degenerate over a brief, 2-day period. Lysosomes and autophagic vacuoles appear in cells of the wing epithelium shortly after it retracts from the pupal cuticle. Hemocytes actively participate in removing the resulting cellular debris. By contrast, epithelial cells in wings of developing adult males of O. leucostigma do not undergo massive cell death. Wing epithelium of female pupae transferred to male pupal hosts behaves autonomously in this foreign environment. By pupation, cells of the female wing apparently are committed to self-destruct even in a male pupal environment. Normal interactions among epithelial cells within the plane of a wing monolayer as well as between the upper and lower monolayers of the wing are disrupted in female O. leucostigma by massive cell degeneration. Despite this disruption, the remaining cells of the wing contribute to the formation of a diminutive, but reasonably proportioned, adult wing with scales and veins.

Animals↗
PubMed1988

A test of positional properties of avian wing-bud mesoderm.

Supernumerary wing structures are readily produced by grafting pieces of wing-bud mesoderm into different locations of host wing buds, but the mechanism underlying their formation remains obscure. The major aim of this study was to examine the ability of posterior quail wing-bud mesoderm, cultured in vitro long enough to lose ZPA (zone of polarizing activity) activity, to stimulate or participate in the formation of supernumerary structures when grafted into anterior slits of host chick wing buds. Small pieces of anterior and posterior quail wing-bud mesoderm (HH stages 21-23) were placed in in vitro culture for up to 3 days. After 2 days, ZPA activity of cultured mesoderm was lost. After the grafting of 2- to 3-day cultured anterior quail wing-bud mesoderm into posterior slits of host chick wing-buds, a consistently high percentage (70%-90%) of grafts result in formation of supernumerary cartilage; in this experiment, however, only a low percentage of grafts resulted in supernumerary cartilage when 2- to 3-day cultured posterior mesoderm was grafted into anterior slits. Taken with controls, these results show that positional differences exist between cultured anterior and posterior wing-bud mesoderm. Serial-section analysis of numerous operated wings has shown several patterns of contribution to supernumerary structures by cells of graft and host. Single supernumerary digits induced by grafts of ZPA mesoderm into anterior slits were normally composed entirely of host cells, but graft cells regularly contributed to skeletal elements of more complex supernumerary structures. Cartilage rods produced by anterior-to-posterior grafts were composed mostly of graft cells, but cartilage nodules and the bases of some rods were often mosaics of chick and quail cells. The results support the proposition that mesodermal cells of the quail wing-bud possess a form of anteroposterior positional memory, but its nature and the means by which the memory of grafted cells interacts with host mesoderm are still not clear.

Animals↗
PubMed1987

Development of wing-bud-derived muscles in normal and wingless chick embryos: a computer-assisted three-dimensional reconstruction study of muscle pattern formation in the absence of skeletal elements.

The mechanisms whereby the normal pattern of muscles within the developing chick limb bud is generated are largely unexplored. It has been proposed that the muscle pattern is established independently of the pattern for the limb skeletal elements to which the muscles normally attach (Shellswell and Wolpert: "The Pattern of Muscle and Tendon Development in the Chick Wing."In: Vertebrate Limb and Somite Morphogenesis. Cambridge University Press, Cambridge, pp. 71-86, 1977). To further examine this possibility we studied the formation of the proximal wing muscles in normal and wingless chick embryos. The muscles of the shoulder region (including the pectoralis) arise as part of the dorsal and ventral premuscle masses of the developing limb bud. These secondarily migrate out of the limb to take origin from the pectoral girdle while inserting onto the humerus (Sullivan: Aust. J. Zool., 10:458-516, 1962). With rare exceptions, wingless embryos have complete absence of wing skeletal elements, but they may possess more than 40% of the normal volume of wing-bud-derived muscles. The muscles that remain in wingless embryos are primarily shoulder muscles, and to a varying extent, the pectoralis. The question we sought to answer was whether in wingless embryos the proximal wing muscles could form a normal pattern in the absence of the humerus and distal wing skeletal elements. By examining three-dimensional reconstructions of the proximal wing region in normal and wingless embryos, we found that the initial subdivision of the dorsal and ventral premuscle masses proceeded normally in the absence of the wing skeleton. This resulted in a grossly normal pattern of proximal wing muscles despite the absence of wing skeletal elements. However, some subsequent cleavages of individual muscles within premuscle mass divisions did not occur in wingless embryos. This suggests that the skeleton may be required for this step in muscle morphogenesis to occur. We also observed that the wing-bud-derived muscles in wingless embryos were nearly always anchored to the pectoral girdle at both ends. Sometimes this resulted in muscles making abnormal tendonous fusions with other muscles derived from the opposite (i.e., dorsal or ventral) premuscle mass. Therefore, attachment to the skeleton may be important for some facet of muscle development. Finally, the supracoracoideus muscle was absent in all but one wingless embryo we examined in the present study. In that one, it was substantially reduced in volume compared to normal. absence of this muscle, the space normally occupied by the supracoracoideus was maintained beneath the pectoralis.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1992

Photoperiod and the relationship between wing length and body weight in Anopheles quadrimaculatus.

The effect of photoperiod on wing length, body weight, and relationship between wing length and body weight was investigated in the mosquito species Anopheles quadrimaculatus. Individuals reared under a short photoperiod (8 h light: 16 h dark) had longer wings and larger weights than did those reared under a long photoperiod (16 h light: 8 h dark). Covariance analysis showed that photoperiod and wing length interacted so that photoperiod did not have a uniform effect on body weight at all wing lengths. At small mosquito sizes, body weight was higher in short than in long-photoperiod individuals of the same wing length, but at large mosquito sizes, body weight was higher in long than in short-photoperiod individuals of the same wing length. Thus, among smaller mosquitoes of this species, wings were disproportionately longer in long-photoperiod individuals, but among larger mosquitoes, wings were disproportionately longer in short-photoperiod individuals. These results, together with previous studies, suggest that photoperiod and temperature have similar effects on the developing insect.

Analysis of Variance↗
PubMed1988

Wings in the intershaft space contribute to the Mueller-Lyer illusion.

The interference of the wings of the wings-in part of the Mueller-Lyer figure was examined for the version of the illusion in which one part of the figure is placed above the other. Wings were removed in pairs from either above or below the shaft of one of the two parts of the figure. Subjects indicated the apparent difference between the lengths of the shafts of the two parts of the figure. Removal of the wings between the shafts of the wings-in part of the figure reduced the amount of the illusion more than removal of the wings from outside the shafts. Removing wings from the wings-out part of the figure reduced the amount of illusion, but it made no difference whether the wing removal occurred between or outside the shafts.

Humans↗
PubMed1976

An analysis of muscle weight variations in the wing and leg of Sturnus vulgaris.

Dry weights of 18 wing and 23 leg muscles from both sides of 15 adult male starlings (Sturnus vulgaris) were determined. By means of factor analysis it is calculated which part of the variance in a muscle's weight can be accounted for by common factors and which part by the characteristics of the muscle itself (residual variance). Wing and leg muscles are analysed separately. From the wing muscle analysis one can draw the following inferences: 1. Three hierarchically ordered factors represent 66%, 8% and 6% of the total variance in the wing muscles. The first common factor will most likely reflect the size variation of the starlings. 2. It appeared advisable to perform rotation of the original factor solution because the second and third factor are bipolar. 3. The three rotated factors can not be interpreted as embryological sources of weight variations and are not related to the segmental or peripheral innervation of the muscles, but generally correspond with three groups of actions that the wing muscles perform. 4. Muscles correlated with the first rotated factor generally move the humerus, while muscles that move the forearm and (parts of) the hand are correlated with the third and second rotated factor, respectively. From the leg muscle analysis it follows that: 1. Five hierarchically ordered factors represent 57%, 13%, 7%, 6% and 4% of the total variance in the leg muscles. Body size (factor 1) plays a more important role in the wing than it does in the leg. 2. It was advisable to rotate the original factor solution since four bipolar factors are present. 3. As in the wing, residual variance shows no particular relation with the mean weight of a muscle. 4. As in the wing, the five rotated factors can only be related to five groups of muscle actions. 5. Muscles correlated with the five rotated factor cause protraction, adduction or inward rotation of the leg or combinations of these movements, whereas muscles correlated with the fourth rotated factor can perform the antagonistic actions. Muscles related to the third rotated factor flex the tarsometatarsus of flex more digits simultaneously, while muscles related to the second rotated factor flex a single digit or extend the tarsometatarus. The fifth rotated factor is a peculiar one since only the mm. peronei are correlated with it. The possibility to apply factor analysis also to experimental stimulated hypertrophy studies and to interspecific muscle weight analyses is discussed.

Animals↗