PubMed Health⌕ Search

Biomedical subjects

A Donjacour

Publications and source records attributed to A Donjacour.

4 recordsLinked to original sources

Role of epithelial-mesenchymal interactions in the differentiation and spatial organization of visceral smooth muscle.

Uterine mesenchyme from newborn (0-day) rats was grown in association with epithelia from the adult cornea, urinary bladder, oesophagus, mammary gland, 1-day skin, and 1-day uterus. Following 1 month of growth, the differentiation of uterine mesenchyme into actin-positive smooth muscle cells was assessed immunocytochemically with antibodies to smooth muscle actin. Whereas grafts of uterine mesenchyme produced only small amounts of myometrium, all types of epithelia induced extensive myometrial differentiation in the uterine mesenchyme, which indicates that this effect is non-specific. The role of cell-cell interactions in the morphological patterning of smooth muscle layers was assessed by analysing tissue recombinants composed of adult prostatic epithelium (PRE) plus mesenchyme of the urogenital sinus (UGM), or seminal vesicle (SVM), or adult bladder epithelium (BLE) plus UGM or SVM. Prostatic ducts developed in all of these tissue recombinants (UGM + BLE, SVM + BLE, UGM + PRE and SVM + PRE). When UGM was used (UGM + PRE and UGM + BLE recombinants), actin-positive smooth muscle cells became organized into thin sheaths resembling the prostatic pattern. Conversely, when SVM was grown in association with PRE or BLE, the induced prostatic ducts were surrounded by thick layers of smooth muscle cells exhibiting the seminal vesicle pattern of organization. Smooth muscle cells were unorganized in grafts of SVM or UGM alone. These observations suggest that in male urogenital glands the mesenchyme dictates the spatial organization of the smooth muscle layers.(ABSTRACT TRUNCATED AT 250 WORDS)

Actins↗

A morphological study of the epididymides of control and estradiol-treated prepubertal dogs.

Treatment of laboratory beagles with 400 micrograms of estradiol benzoate every fourth day from 5 to 20 wk of age severely alters the gross and microscopic morphology of the epididymis. Both stroma and epithelium are affected by estradiol treatment. The peritubular cells of treated animals appear to be fibroblasts separated by broad expanses of collagen, while the control peritubular cells resemble smooth muscle cells separated by small amounts of collagen. The single epithelial cell type present in the treated pup is low columnar and relatively undifferentiated in appearance. These cells appear to be synthetically active based on the accumulation of material within the lumen. The junctions of the epithelial cells of treated animals are occluding, but those of the control are not. The epithelium of control epididymides is composed of columnar principal cells in the caput epididymidis, and principal cells and basal cells in the pseudostratified epithelium of the corpus and cauda epididymidis. The epididymis of the intact, prepubertal dog is responsive to increased estrogen. The presence of estrogen and progesterone receptors (Jones and Connell, 1982) as well as androgen receptors (Younes et al., 1979) suggests that estrogens, progestins, and androgens all may play an essential role in the normal differentiation of the prepubertal epididymis. This is the first description of the ultrastructure of the epididymis of the 20-wk-old dog and the first description of the effect of chronic estrogen treatment on the ultrastructure of the epididymis of the intact prepubertal dog. We propose that the prepubertal dog epididymis is an excellent model system for the study of the hormonal control of epididymal differentiation and development.

Animals↗