Robert L. Searls

A description of chick wing bud development and a model of limb morphogenesis

Abstract The location of the prospective cartilage-forming regions in the embryonic chick wing bud was ascertained by implantation of blocks of wing mesenchyme labeled with tritiated thymidine during the early stages of wing development. The position of the implanted cells was determined by autoradiography, and the location of the implanted block in the limb and its relation to the cartilaginous bones was determined by reconstruction of the host limb from serial sections. The areas corresponding to all of the future wing bones, including the digits, were mapped at each stage from stage 18 to stage 24. Growth of the wing and the prospective bone areas was found to be almost exclusively parallel to an axis perpendicular to the base of the limb. The rate of growth in all areas of the wing reflected the rate of cell division, and all changes in the rate of growth corresponded to changes in the number of dividing cells in the wing and each of the prospective bone regions. Differentiative changes and changes in the growth rate are initiated at a constant distance of 0.4-0.5 mm from the apical ectodermal ridge. These results, considered in conjunction with results of earlier studies in this and other laboratories, suggest that the definitive morphogenetic pattern of the limb arises from four component processes; polarized growth, changes in cell proliferation, cell death, and cytodifferentiation.

The initiation of limb bud outgrowth in the embryonic chick

Abstract Changes in the rate of cell division that occur during the initiation of outgrowth of the embryonic chick wing have been investigated by determination of changes in the labeling index in the wing region and the flank region. It has been found that the labeling index changes very little in the wing region between stage 16 and stage 20, but decreases rapidly in the flank region during the same period. The decrease in labeling index in the flank region results from a change in the proliferative index in that region from 100% at stage 16 to 75% at stage 19. This change in the proliferative index in the flank cannot be easily correlated with differentiative changes in the flank, but correlates very well with morphological changes.

Sulfated mucopolysaccharide synthesis during the development of Rana pipiens

Abstract Sulfated mucopolysaccharide (MPS) synthesis during the development of Rana pipiens was studied autoradiographically and biochemically following injection of embryos with 35 S-sulfate. 35 S-sulfate incorporation can be detected in unfertilized and fertilized eggs. The sulfate-incorporating material accumulates along the periphery of yolk platelets of eggs. During cleavage, the 35 S-sulfate-incorporating material accumulates on cell surfaces as well as along the periphery of yolk platelets. Biochemical analysis utilizing the enzymes chondroitinase ABC and AC and nitrous acid degradation indicates that the MPS synthesized during cleavage is approximately 82% heparin and/or heparan sulfate and 18% chondroitin 4-sulfate. During gastrulation, a greatly enhanced incorporation of 35 S-sulfate is observed in the invaginating chordamesoderm and lateroventral mesoderm, and by the end of gastrulation enhanced incorporation can be detected in neural tissue. During this period, chondroitin 6-sulfate synthesis is initiated. Incorporation of 35 S-sulfate is observed in all tissues of the embryo from the beginning of neurulation through hatching. This ubiquitous incorporation is accompanied by an increase in the relative amount of chondroitin 6-sulfate synthesized. During the period following hatching, incorporation is suppressed in some tissues and enhanced in others so that by the late feeding tadpole stage a very high incorporation is observed only in cartilaginous tissue. These results indicate that sulfated MPS synthesis occurs in all stages of development of Rana pipiens , but that significant changes in the rate of synthesis occur in various cell types during gastrulation and after hatching. The ubiquity of sulfated MPS synthesis during the critical early stages of development and the changes in the pattern of synthesis in various cell types suggest that these molecules are involved in a number of embryonic processes.

Formation of cartilage by non-chondrogenic cell types☆☆☆

Abstract Freshly excised embryonic rat skeletal muscle has been shown to form hyaline cartilage when organ cultured upon demineralized rat bone (bone matrix). Since skeletal muscle is composed of fibrous connective tissue (C.T.) as well as muscle cells, the cartilage could arise from either of these sources. The object of this study was to determine whether cartilage arose from fibrous connective tissue or muscle cells, or both, and whether the ability to form cartilage is limited to tissues derived from somatic mesoderm. Control experiments demonstrated that 19-day embryonic rat skeletal muscle formed cartilage when organ cultured on bone matrix after dissociation and cultivation in vitro, and that 11-day embryonic chick muscle also formed cartilage, although less reproducibly (3 out of 10 cases). Fibroblasts and skeletal muscle were cloned from similar suspensions of dissociated muscle in order to test these purified cell types. Dermis, vascular tissue, and tendons were mechanically removed prior to dissociation in order to eliminate fibroblasts from contaminant sources. Cloned fibroblasts, derived from rat skeletal muscle, formed cartilage in three out of three cases. It was not possible to clone sufficient rat skeletal muscle to place an aggregate onto bone matrix. An aggregate of several hundred chick skeletal muscle clones formed cartilage on bone matrix. The freshly excised C.T. capsules of embryonic chick thyroid and lung were tested for the ability to form cartilage as nonskeletal C.T. derivatives. The epithelial rudiments of thyroid and lung were also tested as endodermal derivatives. Chick cornea was similarly tested as an ectodermal derivative. Of these tissues, only the C.T. capsules formed cartilage. The results demonstrate that various C.T. cell types may alter their phenotype well after that stage at which their differentiation is thought to be stabilized, and that the ability to differentiate as cartilage may be common to all C.T. cells. The option of differentiating along a certain variety of pathways may depend more upon local conditions than on a predetermined pattern.

The establishment of the cartilage pattern in the embryonic chick wing, and evidence for a role of the dorsal and ventral ectoderm in normal wing development

Abstract Previous investigations have indicated that the limb bud behaves as a mosaic after some experimental manipulations and regulates after others. In light of new maps of the prospective cartilage-forming regions of the chick wing, we have reinvestigated the stability of the limb pattern by two experimental procedures. First, the prospective long bone regions were excised to examine the ability of the cells outside of the prospective long bone regions to form normal long bones. Second, the mesoderm, mesoderm + dorsal and ventral ectoderm, or dorsal ectoderm (with a small amount of subjacent mesoderm) of the prospective elbow region were rotated 180° to examine the ability of the limb to control and regulate the differentiation of the cells in the limb. We can conclude from these experiments that the cartilage-forming regions of the limb mesoderm gradually become stabilized between stage 22 and stage 24, and that the stabilization is due to the advanced state of differentiation and to the decreased rate of cell division after stage 22. In addition, the dorsal and ventral ectoderm have been shown to aid in stabilization of the cartilage pattern and to influence the development of the humerus. We conclude that the dorsal and ventral ectoderm play a significant role in limb development.

Differentiation of the thyroid in the hypophysectomized chick embryo.

Abstract The influence of hypophyseal hormones on the normal development of the thyroid gland was investigated by decapitating chick embryos at a time before the hypophysis has begun to form. Thyroids from decapitated embryos were compared with thyroids of normal embryos from shortly after decapitation to the time when the embryo should hatch. The thyroids were examined for ultrastructural differences and for accumulation of thyroglobulin. Thyroxine levels in the blood were also examined. It was concluded that the thyroids in decapitated embryos develop normally up to about 12 days of development, by which time morphogenesis and differentiation of the gland is essentially complete. The rates of thyroid growth and accumulation of thyroglobulin are diminished after 12 days of development. The amount of thyroxine in the blood is decreased by about one-half. Thyroxine was found in the yolk of unincubated eggs at levels sufficient to sustain blood thyroxine levels throughout embryonic development. We conclude that hormones that are synthesized by the embryonic hypophysis affect thyroid development only through their influence on generalized growth and metabolic activity.

Developmental Changes in Tracheal Structure

ABSTRACT: Mechanical properties of the proximal airways are known to change with development; the highly compliant airways of the immature animal become stiffer and less collapsible with increasing age. Although the relationship between tracheobronchial architecture and function has been described for adult physiology, little is known regarding this relationship during early development. This study was, therefore, designed to test the hypothesis that alterations in tracheal morphometry parallel developmental differences in tracheal functional properties. Tracheal segments obtained from 29 lambs ranging in age from 70% of gestation to full-term newborn lambs up to 6 d old were examined using anatomic, morphometric, and histochemical techniques. The results showed 1) progressive increases in the dimensions of the trachea and the tracheal wall components, 2) alterations in the geometric arrangement of the tracheal ring, and 3) changes in the compositional characteristics of the tracheal cartilage with maturation. These findings demonstrate alterations in tracheal architecture, each of which contribute to the greater stiffness of the trachea, in older animals. When considered together, these factors help explain the differences in tracheal functional characteristics with development.

The mechanism of cervical flexure formation in the chick

SummaryChick embryos, during stages 14 to 25, undergo an arching of the hindbrain and cervical neural tube that is termed cervical flexure. We have found that if the truncus arteriosus is severed during stage 12–13, the embryos survive for more than 24 h and do not show cervical flexure. The embryos have a beating heart, the expected number of somites, and often have discernible wing and leg buds. Light and electron micrographs reveal no histological abnormalities. The percentage of cells that become labeled with tritiated thymidine is close to normal, indicating that most of the cells are healthy. These results suggest that cervical flexure is related to normal morphogenesis of the heart. At stage 10, the heart is almost straight, with the prospective ventricle cranial to the prospective sinus venosus. The heart tube loops between stage 10 and stage 23, first to the right and then caudad, so that the ventricle becomes caudal to the sinus venosus. The heart undergoes these morphogenetic movements autonomously. The truncus arteriosus does not increase in length during caudal movement of the ventricle, so the cervical region is pulled into an arch. Bending of the cervical region into an arch can be prevented in intact embryos by injecting agar into the foregut, so that the foregut cannot bend. However, after about 24 h of further growth, if the axis cannot bend, the truncus begins to leak blood and the embryo dies. We conclude that cervical flexure is a response of the embryonic axis to the morphogenesis of the heart.

Effects of β-D-xyloside on differentiation of the respiratory epithelium in the fetal mouse lung

Differentiation of respiratory endings in the fetal lung appears to be controlled by its surrounding mesodermal capsule. The capsule may exert its influence by controlling the composition of the epithelial basal lamina or of the extended extracellular matrix that is deposited during the period when alveolar sacs are formed. As a first step in testing this hypothesis, the effects of the drug, rho-nitrophenyl-beta-D- xylopyranoside (beta-xyloside), an inhibitor of proteoglycan synthesis, and its inactive alpha anomer (alpha-xyloside) were examined. Lung primordia from mice at 16 days of gestation were tested for inhibition of morphological and functional differentiation as a result of drug treatment. Pseudoglandular lung epithelium did not form respiratory endings, contained fewer specialized cells, and accumulated little additional surfactant when treated with beta-xyloside but developed normally when treated with alpha-xyloside or grown in control medium. The results are interpreted to suggest that deposition of an extracellular matrix rich in proteoglycan is required to support maturation of the respiratory epithelium.

Altered patterns of proteoglycan deposition during maturation of the fetal mouse lung

Previous studies have shown that beta-xyloside inhibits maturation of the fetal mouse lung (Smith et al., Dev. Biol. 138, 42-52, 1990). Insofar as this drug inhibits proteoglycan deposition, the present studies were undertaken to examine the chemical composition and tissue distribution of proteoglycans in order to determine, more precisely, their role during lung morphogenesis. Autoradiography of labeled 16- and 19-day embryonic lungs demonstrated greater incorporation over the mesenchyme. Treatment with beta-xyloside did not alter the autoradiographic appearance; however, beta-xyloside treatment followed by nitrous acid digestion, eliminated most silver grains. Isolation of proteoglycans from extracellular, membrane and intracellular pools over the 16- to 19-day interval demonstrated redistribution of heparan sulfate proteoglycan from an intracellular to a membrane location, while chondroitin sulfate proteoglycan redistributed from intracellular to extracellular. Only the synthesis of chondroitin sulfate proteoglycan was inhibited by beta-xyloside. On the basis of these results we suggest that a chondroitin sulfate proteoglycan is required for lung maturation and that inhibition of its synthesis results in inhibition of septa formation and subsequent failure of morphogenesis and differentiation.