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During human foetal brain vascularization, activated CD31+/CD105+ endothelial cells are characterized by the emission of filopodial processes which also decorate the advancing tip of the vascular sprout. Together with filopodia, both the markers also reveal a number of plasma membrane-derived microvesicles (MVs) which are concentrated around the tip cell tuft of processes. At this site, MVs appear in tight contact with endothelial filopodia and follow these long processes, advancing into the surrounding neuropil to a possible cell target. These observations suggest that, like shedding vesicles of many other cell types that deliver signalling molecules and play a role in cell-to-cell communication, MVs sent out from endothelial tip cells could be involved in tip cell guidance and/or act on target cells, regulating cell-to-cell mutual recognition during vessel sprouting and final anastomosis. The results also suggest a new role for tip cell filopodia as conveyor processes for transporting MVs far from the cell of origin in a controlled microenvironment. Additional studies focused on the identification of MV content are needed to ultimately clarify the significance of tip cell MVs during human brain vascularization.

The involvement of the metalloprotease-2 (MMP-2) in vessel development was investigated in the human telencephalon by double immunoreactions with antibodies to the enzyme, latent (proMMP-2) and active (aMMP-2) forms, and an antibody against collagen type IV, a constitutive component of the extracellular matrix (ECM) of the vessel basal lamina. MMP-2 is expressed in both 12- and 18-week telencephalic vessels, the proenzyme being mainly localised in endothelial cells and the active form prevailing in alpha-actin-reactive periendothelial cells identified as pericytes. Endothelial cells intensely positive for aMMP-2 were revealed in some microvessels and appeared locally associated with discontinuities of the collagen basal lamina. No detectable expression of MMP-2 was observed in perivascular glial processes revealed by vimentin/glial fibrillary acidic protein immunostainings. Double immunoreactions performed to further investigate telencephalon angiogenesis have demonstrated that both the endothelial cells and pericytes strongly express vascular endothelial growth factor (VEGF). Taken together, the results indicate that MMP-2 is largely involved in human brain angiogenesis and suggest that endothelial cells and pericytes tightly interplay in both angiogenesis mechanisms, by ECM proteolysis, and angiogenesis regulation, by local (autocrine/juxtacrine) VEGF action.

The pericytes have been ultrastructurally and morphometrically analyzed in the neural vessels of the chick embryo optic tectum, under the transmission and scanning electron microscopes. The observations demonstrated that shape and surface features of pericytes, as well as their spatial relation with the endothelium, remarkably change during development, whereas their ultrastructure does not substantially modify from the early to the late embryonic stages. The pericytes have an ovoid body, broad processes, smooth surfaces, and are closely applied to the endothelial tube on days 5-7; they show convolute shape, highly irregular surfaces, and are complicately interdigitated with the endothelial cells, when a vivacious vessel growth takes place, on days 12-14; finally, they are flattened, smooth, highly branched, and completely enclosed in the basement lamina on days 20-21, when a definitive vascular pattern is established. The contribution of pericytes to the formation of the basement lamina has been confirmed by the detection of exocytotic vesicles discharging their content toward the subendothelial cleft. The morphometric evaluations revealed that pericytes provide the growing neural microvessels with an almost continuous coverage which, however, undergoes a significant reduction within hatching time. On the whole, the results suggest that the pericytes are as active as the endothelial cells during the vessel growth and play an inhibitory role on the endothelial proliferation only later on, when they are closely adherent to the endothelium and are encompassed by the basement lamina.

The spatial relationship established between glial cells and microvasculature in the human cerebral cortex was analysed on peritumoral tissue of the parietal lobe removed during surgery. Observations performed by light microscope immunocytochemistry demonstrated that processes of astrocytes, strongly immunoreactive to both glial fibrillary acidic protein and S-100 protein, form sheaths to the capillaries, and that isolated cells positive to the oligodendrocyte marker 2',3'-cyclic nucleotide 3'-phosphodiesterase are detectable in perivascular areas. Morphometrical analysis by transmission electron microscopy showed that 80% of the vascular endothelium-pericyte layer is invested by small endfeet of astrocyte processes. This study demonstrates that either astrocyte bodies or oligodendrocytes as well as microgliocytes may substitute the astrocytic endfeet adhering to the capillary basement lamina.

The role played by perivascular astrocytes in neural vessel maturation was investigated in microvessels of the chick embryo optic tectum. Three-dimensional reconstructions and quantitative analyses were made, and permeability was studied. On embryonic days 14-16, 12.5% of the microvessel wall is surrounded by astrocyte endfeet which, in most cases (82%), are located under endothelium junctions; the latter, at this stage, partly prevent the extravascular escape of the marker horseradish peroxidase. On days 18-21, the astrocyte processes form a nearly complete perivascular sheath enveloping 96% of the microvessel perimeter; the junctions of the endothelial cells are much wider and impermeable owing to extensive fusion of the endothelial plasma membranes. This investigation suggests a close relationship between the perivascular arrangement of glia and differentiation of the endothelium tight junctions and indicates that the morphofunctional maturation of the latter takes place progressively during the prenatal organogenesis of the chick central nervous system.

The modifications of the endothelial surfaces were analyzed in growing neural microvessels by scanning and transmission electron microscopes in the optic tecta of chick embryos and chickens. The endothelial inner aspect appears regular and smooth in the early stages of the vessel growth (7th incubation day). Later (14th incubation day) both the abluminal and luminal surfaces of the endothelium follow a very sinuous course and the luminal ones appear extremely rich in pleomorphic microprojections. When the endothelium differentiation is concluded (5-day-old chicken), the cells are very thin and again exhibit regular and smooth surfaces. These findings reveal a great mobility of the cell membrane of the endothelial cells when they are growing longer and thinner by a moulding process. Moreover, the presence of a number of pinocytotic pits in the embryo vessels would indicate that the neutral vessels, provided with a typically low pinocytotic activity in the adult life, are engaged in this function during development.

The mode and the temporal sequence of the modifications undergone by permeability-related structures in the neural microvessels have been ultrastructurally and morphometrically investigated in optic tecta of 6, 14, and 18 incubation day (i.d.) chicken embryos and of 30 day chickens. Horseradish peroxidase was utilized as a permeability marker. The endo- and exocytosis-related structures (vesicles and vacuoles) and the interendothelial junctions remarkably change during development: the density of the vacuoles is decreased at the 14th i.d., while that of the vesicles becomes significantly low at the 18th i.d., both reaching lowest values in the chicken; the passage of the marker through the endothelial junctions begins to be hindered from the 14th i.d., parallel to the perivascular arrangement of astrocytic glia endfeet, and it is completely blocked at hatching time. The findings suggest that the optic tectum microvessels are permeable, and thus immature, in the early development and progressively acquire morphofunctional features of vessels provided with barrier devices during the pre- and post-natal development of the brain.

Basement lamina and pericytes of growing blood microvessels were analyzed in the chick embryo optic tectum, from the 8th incubation day to hatching. Formation of the basement lamina and morphological changes of the pericytes take place in a short range of time, but late in the embryonic life, when also the blood brain barrier (bbb) devices are developing. The spatial and temporal coincidence between basement lamina formation, endothelium tight junction differentiation, and perivascular arrangement of the astrocytic glia, indicates that these events are correlated and corroborates the hypothesis that the glia needs an extracellular matrix to induce the junctional system maturation in the neural endothelia. Pericytes are irregular in shape during the early neural angiogenesis and smooth and flattened later, as the basement lamina synthesis is taking place; these cells represent a second line of barrier beyond the endothelium when the bbb is immature, owing to their phagocytic and digestive properties.

The vesicles and vacuoles of the endothelia, morphological expression of endocytosis and transendothelial transport, are quite absent in the mature neural endothelia. In order to study the temporal sequence of the vesicle and vacuole modifications during the blood brain barrier (bbb) setting up, the extent of these structures was morphometrically analyzed on electron micrographs of neural microvessels in the optic tectum of 8, 14, and 17 day chick embryos, fixed after an intracardial injection of the permeability marker horseradish peroxidase. During the development, endocytosis and transendothelial transport change, since a statistically significant reduction of both vesicles and vacuoles was recorded at the 17th incubation day. The temporal coincidence between decrease of endocytosis-transport processes and appearance of astrocytic endfeet close to the vessel wall, suggests that the glial cells might control, besides the tight junction formation, the expression of other properties of the bbb-provided endothelia.