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Query: UNIPROT:P01178 (oxytocin)
 15,767 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Using immunocytochemistry and electron microscopy, we demonstrate that oxytocin (OT) exerts a trophic effect on its target myoepithelial cells in the mammary gland. In vitro, in organotypic cultures of mouse mammary gland, we examined proliferation and differentiation of the different cell types induced by OT added to the medium. In vivo, we studied the effect of OT on the structure and cell composition of developing glands. Uptake of 5-bromo-2'-deoxyuridine was used as proliferation marker, while antibodies to smooth muscle alpha-actin (specific for myoepithelial cells) and keratin (MoAb AE1; selective for epithelial cells) were used to identify differentiated cell types. By electron microscopy, we studied structural modifications induced by OT on the extreme projections of the developing gland (sc end buds). The results indicate that OT induces myoepithelial cell differentiation and proliferation, enhancing the effect of mammotrophic hormones in nonlactating mouse mammary gland. A less marked effect was observed in luminal epithelial cells. No significant effect of OT alone was detected in cultured glands from unprimed animals.
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PMID:Oxytocin enhances myoepithelial cell differentiation and proliferation in the mouse mammary gland. 834 20

The neurohypophysial peptide hormone [Arg8]vasopressin (AVP) has well documented pressor effects in the periphery. These are mediated by vasopressin receptors (VPRs) of the V1a subtype, expressed by vascular smooth muscle cells, which induce vascular contraction when activated. AVP also has effects on the vasculature of the brain, where it has been reported to induce both vasodilation and vasoconstriction. The responsiveness of blood vessels of the spinal cord, however, has received little attention. To determine the morphology and distribution of blood vessels within the spinal cord, vessels were vizualised using a mouse anti-rat smooth muscle alpha actin IgG as primary antibody and fluorescein isothiocyanate-conjugated anti-mouse IgG secondary antibodies. A complementary vizualisation strategy which detected the endogenous peroxidase activity of red blood cells within vessels was also utilised. The characteristics of the structures observed using both visualisation strategies were typical of blood vessels. VPRs were localized using recently characterized high affinity biotinylated analogue of AVP (PhAcAL(Btn)VP), which is selective for the V1a subtype of VPR. PhAcAL(Btn)VP:VPR complexes were subsequently visualized by avidin-Texas red. The pharmacological characteristics of these sites were established using selective analogues of vasopressin and oxytocin. This confirmed that V1a receptors were indeed being visualized. The structures observed following visualization of VPRs had the same morphology as the vasculature revealed by the anti smooth muscle alpha-actin antibody. It can therefore be concluded that the blood vessels of the spinal cord express VPRs and are potentially responsive to AVP. Furthermore, VPRs were detected on capillaries of the microvasculature. As these capillaries are devoid of smooth muscle, VPRs must be expressed by endothelial cells as well as by smooth muscle cells. This distribution of VPRs would enable AVP to regulate local blood flow. The source of the AVP could be the general circulation, or perhaps more likely, to be local release from vasopressinergic hypothalamic neurones which are known to innervate specific regions of the spinal cord.
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PMID:Intramedullary blood vessels of the spinal cord express V1a vasopressin receptors: visualization by a biotinylated ligand. 875 Dec 90

The myometrium undergoes substantial remodeling at the time of labor including rearrangement of the cellular contractile machinery. The regulation of this process in human myometrium at the time of labor is poorly defined, but evidence in other muscle types suggests modulation by small heat shock proteins (sHSP). The aim of this study was to investigate whether similar changes in sHSP occur in the myometrium at labor. Using a quantitative proteomic approach (two-dimensional difference gel electrophoresis), we found a 69% decrease in the sHSP alphaB-crystallin in the myometrium at labor plus multiple isoforms of HSP27. Immunoblotting using phosphospecific HSP27 antibodies (HSP27-serine15, -78, and -82) detected marked changes in HSP27 phosphorylation at labor. Although total HSP27 levels were unchanged, HSP27-Ser15 was 3-fold higher at labor. Coimmunoprecipitation studies showed that HSP27 coprecipitates with alphaB-crystallin and also smooth muscle alpha-actin. Coimmunofluorescence studies demonstrated a relocation of HSP27 from the perinuclear region to the actin cytoskeleton at labor. The functional significance of these changes was demonstrated in vitro where myometrial strips stimulated to contract with oxytocin exhibited increased HSP27-Ser15 phosphorylation. Our findings provide data consistent with a novel pathway regulating human myometrial contraction at labor and identify HSP27 and alphaB-crystallin as potential targets for future tocolytic design.
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PMID:Contraction in human myometrium is associated with changes in small heat shock proteins. 1791 31

Mammary myoepithelial cells are specialized smooth musclelike epithelial cells that express the smooth muscle actin isoform: smooth muscle alpha-actin (ACTA2). These cells contract in response to oxytocin to generate the contractile force required for milk ejection during lactation. It is believed that ACTA2 contributes to myoepithelial contractile force generation; however, this hypothesis has not been directly tested. To evaluate the contribution of ACTA2 to mammary myoepithelial cell contraction, Acta2 null mice were utilized and milk ejection and myoepithelial cell contractile force generation were evaluated. Pups suckling on Acta2 null dams had a significant reduction in weight gain starting immediately postbirth. Cross-fostering demonstrated the lactation defect is with the Acta2 null dams. Carmine alum whole mounts and conventional histology revealed no underlying structural defects in Acta2 null mammary glands that could account for the lactation defect. In addition, myoepithelial cell formation and organization appeared normal in Acta2 null lactating mammary glands as evaluated using an Acta2 promoter-GFP transgene or phalloidin staining to visualize myoepithelial cells. However, mammary myoepithelial cell contraction in response to oxytocin was significantly reduced in isolated Acta2 null lactating mammary glands and in in vivo studies using Acta2 null lactating dams. These results demonstrate that lack of ACTA2 expression impairs mammary myoepithelial cell contraction and milk ejection and suggests that ACTA2 expression in mammary myoepithelial cells has the functional consequence of enhancing contractile force generation required for milk ejection.
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PMID:Myoepithelial cell contraction and milk ejection are impaired in mammary glands of mice lacking smooth muscle alpha-actin. 2136 98