Muscle cell death during the development of head and neck muscles in the chick embryo.

Degenerating myofibers have been reported in the embryos and neonates of a number of birds and mammals, but neither the pervasiveness of the phenomenon nor the spatio-temporal patterns of degeneration has been examined in detail. Using transmission electron microscopy, we determined the patterns of muscle cell death in the chick biventer cervicis, a head extensor muscle. Cell death is most pronounced at incubation days 10 through 15, and occurs throughout the muscle. This is the period during which many myofiber clusters segregate into individual fibers, each with a separate basal lamina, and secondary myofibers become demarcated. Cells of largest diameter, presumably the primary myofibers, are preferentially affected. Degenerating cells exhibit a cohort of cytological features consistent with apoptosis, including the presence of dense, darkly-staining, hypercontracted myofibrils, misshapen nuclei with irregular chromatin condensations along the nuclear envelope, and scores of cytoplasmic vesicles and vacuoles. In cross section some large diameter muscle cells are characterized by sparse, flocculent cytoplasm that is devoid of myofibrils and organelles. Some show disintegrating cell membranes. In longitudinal section 200-300 microns long regions of hypercontracted myofibrils alternate with areas devoid of fibrils; this arrangement suggests that the myofibrils break into segments that are in register along one part of a muscle fiber and entirely absent from the adjacent length of fiber. We have observed similar patterns of muscle cell degeneration in the complexus, splenius cervicis, depressor mandibulae, and branchiomandibularis muscles. By day 18 of incubation most signs of degeneration are absent and by hatching (day 21) the muscle fibers all appear healthy. Many of these cytological changes in embryonic head muscle cells are characteristic of programmed cell death. We hypothesize that large-scale death of myocytes is a normal part of avian myogenesis and an important mechanism for affecting the transformation from embryonic to hatching muscle patterning.

Comparative embryonic development in chickens with different patterns of postnatal growth.

We compared embryonic development of two lines of chickens that exhibit different patterns of postnatal growth. Classical staging techniques and morphological measurements of bone, cartilage, feather and intestines were used to test the hypothesis that differences in postnatal growth would be reflected in patterns of embryonic tissue partitioning. During the second quarter of incubation, the line with higher postnatal growth staged significantly earlier (i.e., was less developed overall) than the line with lower postnatal growth. Embryos from the line with higher postnatal growth exhibited less (i.e., allocated away from), bone growth (beak length, ossification of long bones), feather growth (number of feather papillae, length of primary), and eye development (number of lens sclera). There were no differences in gut development between the two lines. Our results show that different postnatal growth patterns are associated with changes in the pattern of embryonic reallocation between tissue types, even when gross morphological differences are not evident at hatching. We suggest that these differences in development represent periods when the embryo is allocating to hyperplastic growth of tissues such as muscle, as a means of increasing posthatching growth potential.

Ontogeny of architectural complexity in embryonic quail visceral arch muscles.

Understanding the mechanisms of muscle pattern formation requires that the complete sequence of ontogenetic events be defined, particularly in the emergence of architectural complexity and in the spatial relations between muscles and skeletal elements. This analysis of visceral arch myogenesis in quail (Coturnix coturnix japonica) embryos identifies the location of premuscle condensations and subsequent segregation of individual muscles, documents the initial orientation of myofibers and changes in alignment associated with maturation, and describes the spatial and temporal relations between muscle development and the formation of connective tissues. Premuscle condensations form within the visceral arches on embryonic days 2-4, before skeletal elements make their appearance. Discrete muscles may form from the subdivision of a muscle mass after fiber orientations have been established (e.g., jaw adductor and hyobranchial muscles) or by the segregation of a mesenchymal cluster from the condensation prior to the appearance of oriented fibers (e.g., protractor, muscle of the columella). The rate and pattern of subsequent muscle maturation are closely associated with the development of the hard tissues. Myogenesis in 4-9-day embryos centers around the quadrate cartilage, the retroarticular process of the mandibular (Meckel's) cartilage, and the epibranchial cartilage. Muscles form attachments on these elements and remain without additional attachments until the appropriate elements (e.g., otic capsule, pterygoid bone) develop. No single description of myogenic events applies to all visceral arch muscles, nor is there an arch-specific pattern of ontogeny. Rather, each muscle has distinctive characteristics based on its spatial relations within the developing head.

Anatomy of raccoon (Procyon lotor) and coati (Nasua narica and N. nasua) forearm and leg muscles: relations between fiber length, moment-arm length, and joint-angle excursion.

Muscle architecture, moment arms, and locomotor movements in the distal limb segments of the procyonids Nasua (coati) and Procyon (raccoon) are analyzed with reference to patterns of muscle fiber length. This study addresses the hypothesis that relative fiber lengths among muscles in a muscle group can be predicted on the basis of correlates of muscle tension. The results include the following: consistent patterns of fiber length of muscles in a muscle group exist within and between the two genera. Differences in fiber length between muscles can be accounted for by two principal correlates of muscle excursion--length of a muscle's moment arm about a joint and joint-angle excursion. Muscle fiber pinnation permits increased tendon excursion, but this effect is relatively small in comparison to the effects of moment-arm length and joint-angle excursion. Corollary action between two or more joints (or lack thereof) is an important factor in determination of fiber lengths.