Auteur(s) : Claire Michelet‐Habchi, Philippe Barberet, Raj Kumar Dutta, Philippe Moretto, Andrée Guiet‐Bara, Michel Bara , Centre d‘Études Nucléaires de Bordeaux‐Gradignan, Interface Physique‐Biologie, Le Haut‐Vigneau, BP 120, 33175 Gradignan Cedex, France. Laboratoire de Physiologie et Physiopathologie, Université P. et M. Curie, Bât. A, 4 Place Jussieu, 75252 Paris Cedex 05, France. .
Illustrations
Fig. 1.PIXE microanalysis of a
placental artery transverse section. The lumen, in the center of
the map, is bordered by the artery wall. The thick media layer,
composed of vascular smooth muscle cells (VSMCs) may be seen on the
large maps thanks to the contrast in sulphur and chlorine content.
A zoom on the border of the lumen (140 × 140 µm2
maps on the right) shows the monolayer of endothelial cells, rich
in phosphorus and chlorine.
Fig. 2. Histogram plots of the ion
concentrations found in vascular smooth muscle cells (VSMC) of
placental arteries. 3 groups of data are presented: specimens
incubated in Hanks' solution, specimens incubated in Hanks'
solution + MgSO4, specimens incubated in Hanks' solution
+ MgCl2. Error bars indicate standard deviation (*
p < 0.05; *** p < 0.005).
Fig. 3.Histogram plots of the ion
concentrations found in vascular endothelial cells (VEC) of
placental arteries. Results are expressed in terms of concentration
ratios against sulphur, taken as a reference element. 3 groups
of data are presented: specimens incubated in Hanks' solution,
specimens in Hanks' solution + MgSO4, specimens in
Hanks' solution + MgCl2. Error bars indicate standard
deviation (** p < 0.01).