The rhizoplast of chrysomonads, a basal body-nucleus connector that polarises the dividing spindle.

An ultrastructure study of the rhizoplast in Synura petersenii, Mallomonas fastigiata, and M. insignis shows that it consists of 15-20 striated rootlets that form a claw or an incomplete cone over the nucleus. These rootlets course along one face of the nucleus between the nuclear membrane and the cis-face of the Golgi stack of cisternae. They converge and merge above the nucleus, forming a stub attached to the proximal section of the two basal bodies. These cross-striated rootlets are composed of closely packed longitudinal microfibrils. By immunofluorescence, the basal bodies and the rootlets forming the claw were decorated by the anti-centrin monoclonal antibody ICL19 raised against the Paramecium tetraurelia acidic centrin protein and by two antibodies raised against the striated parabasal and costal striated fibres of trichomonads. Only the anti-centrin monoclonal antibody 20H5 raised against Chlamydomonas reinhardtii centrin strongly labelled the 20-22 kDa protein bands from the extracted cytoskeleton of S. petersenii by immunoblotting. Electron micrographs of mitosis in S. petersenii cells revealed that the segregated pairs of basal bodies are linked by the striated rootlets of the rhizoplast to the poles of the mitotic spindle. The spindle microtubules arise perpendicularly from the striated rootlets of the basal body-nucleus connector forming the centrosome. In conclusion, in these cells there is a basal body-nucleus connector similar to that of C. reinhardtii and other chlorophytes. It contains centrin proteins, it is involved in the linkage of the basal bodies to the nucleus and is a component of the spindle pole body or centrosome in the dividing cell.

[New hypothesis on the replication of centrioles and basal bodies]. / Nouvelles hypothèses sur la réplication des centrioles et des corps basaux.

Certain morphological data, obtained in studies of the ultrastructure of centrioles and basal bodies in cells of metazoa and protists, lead us to think that the cartwheel represents of the most appropriate organization for a self-reproducing and transmissible centriolar organizer. Centrioles and basal bodies might then not be simply the centres of replication of those organizers, but also reservoirs containing several superposed centriolar organizers, which are released depending on the requirements of the cell. As an isolated cartwheel is extremely unlikely to be detected, either in conventional electron microscopy or in immunocytochemistry, it is thus the reservoir which has so far been under consideration. Such a hypothesis would permit the explanation that biogenesis de novo and biogenesis in proximity to preexisting organelles may differ only in terms of the number of morphogenetic units involved.

Structural changes and in situ aortic pressure-diameter relationship in long-term chemical-sympathectomized rats.

This study determined the effects of long-term chemical sympathectomy with guanethidine (GN) on the mechanical properties and composition of the distal abdominal aorta in Wistar rats. GN was daily administered for 3 mo (3M-GN, from 1 to 12 wk), 5 wk (5W-GN, from 7 to 12 wk), and 8 days (8D-GN, from 11 to 12 wk). All experiments were performed at 12 wk of age to avoid age differences at examination. We used a high-resolution echo-tracking system to determine in situ, in the systolic-diastolic range, the aortic diameter-, compliance-, and distensibility-pressure curves in anesthetized rats. We observed an equivalent significant fall in the tyramine pressor response in all conscious GN-treated rats. Blood pressure was not affected by sympathectomy after 8 days and 5 wk of treatment but was significantly reduced in 3M-GN rats. Chronic sympathetic denervation increased aortic diameter and compliance in 8D-GN rats, compared with those obtained at the same distending pressure in control rats, suggesting vascular smooth muscle relaxation. In contrast, in 5W-GN and 3M-GN rats, the distensibility pressure-curves were significantly shifted toward lower levels of distensibility and pressure, indicating a decreased aortic distensibility at the same level of arterial pressure. Sympathectomy produced a significant reduction in the content of elastin, one of the most distensible components of the arterial wall in 5W-GN and 3M-GN rats. These results suggest that intact sympathetic nerves are necessary to maintain normal functional and structural properties of large arteries in rat. The reduction in aortic distensibility, in long-term sympathectomized rats, could have resulted from complex interactions between local aortic denervation, change in the set point of distending pressure, and changes in aortic smooth muscle tone and/or wall composition.

[Measurement of the vascular mass of the human radial artery by ultrasonics]. / Mesure de la masse vasculaire de l'artère radiale humaine par méthode ultrasonique.

OBJECTIVE: To determine the reproducibility of radial artery mass (RAM), in hypertensive patients. DESIGN AND METHODS: In 49 patients, RAM was measured using a high resolution echotracking device (Nius-02) which allows noninvasive measurement of diameter and wall thickness of the radial artery. RAM was validated in vitro by comparing weight of arterial segments to ultrasonographic measurement and determined as RAM = r (pi Re2-pi Ri2) where r is the arterial wall density (1.06 g/cm3), and Re and Ri are values of internal and external radii, respectively. Repeatability coefficient (RC2 = SDi2/n) was 1.3 mg. RESULTS: Blood pressure was (mean +/- SD) 146 +/- 19/85 +/- 15 mmHg, radial arterial diameter was 2,449 +/- 376 microns, radial wall thickness was 302 +/- 68 microns, RAM was 28 +/- 9 mg (range 13-43 mg). CONCLUSION: These results indicate that radial artery mass can be measured using a high resolution echotracking device.

Elastic modulus of the radial artery wall material is not increased in patients with essential hypertension.

Hypertension is known to decrease arterial distensibility and systemic compliance. However, the arterial tree is not homogeneous, and it has been shown that the medium-size radial artery does not behave like the proximal, elastic, large, common carotid artery. Indeed, radial artery compliance in hypertensive patients (HTs) has been shown to be paradoxically increased when compared with that in normotensive control subjects (NTs) at the same blood pressure level. To determine whether this increase was due to hypertension-related hypertrophy of the arterial wall, radial artery functional and geometric parameters from 22 NTs (mean +/- SD, 44 +/- 11 years) were compared with those from 25 age- and sex-matched never-treated essential HTs (48 +/- 12 years) by using a high-precision ultrasonic, echo-tracking system coupled to a photoplethysmograph (Finapres system), which allows simultaneous arterial internal diameter, intima-media thickness, and finger blood pressure measurements. When the values for HTs were compared with those of NTs at their respective mean arterial pressures, HTs had similar internal diameter (2.50 +/- 0.56 versus 2.53 +/- 0.32 mm, mean +/- SD) and greater intima-media thickness (0.40 +/- 0.06 versus 0.28 +/- 0.05 mm, P < .001) measurements and increased arterial wall cross-sectional areas (3.79 +/- 1.14 versus 2.45 +/- 0.57 mm2, P < .001). Circumferential wall stress was not significantly different between the two groups. Compliance calculated for a given blood pressure, ie, 100 mm Hg (C100), was greater in HTs than NTs (3.46 +/- 2.41 versus 2.10 +/- 1.55 m2.kPa-1 x 10(-8), P < .05).(ABSTRACT TRUNCATED AT 250 WORDS)

Noninvasive measurement of medium-sized artery intima-media thickness in humans: in vitro validation.

Recent research in ultrasound technology has led to the development of a high-resolution echo-tracking device. The present study was performed to evaluate the accuracy in the measurement of human radial artery intima-media thickness with this new device. We determined the correlation between histological and ultrasonic measurements of intima-media thickness in 15 radial artery segments obtained from the distal end of the wrist-elbow harvest for coronary bypass grafting in patients with coronary heart disease. For arterial intima-media thickness, a positive correlation was observed between ultrasonic and histological measurements (r = 0.618; p < 0.014), and the difference between ultrasound and histology measurements was 41 +/- 66 microns, with the higher measurements found by the ultrasonic device. In a subgroup of 11 patients, we determined the correlation between in vivo ultrasonic measurements of radial artery intima-media thickness at the preoperative stage and in vitro ultrasonic measurements of intima-media thickness obtained postoperatively in the same arterial segments. Internal diameter was larger in vivo than in vitro, and intima-media thickness was smaller in vivo than in vitro. The cross-sectional area of the arterial wall was calculated from internal diameter and intima-media thickness. In vitro wall cross-sectional area was correlated with in vivo wall cross-sectional area (r = 0.929; p < 0.0001). Repeatability of in vivo intima-media thickness measurements was investigated in 10 subjects through the calculation of the repeatability coefficient as defined by the British Standards Institution.(ABSTRACT TRUNCATED AT 250 WORDS)

Spontaneous diameter oscillations of the radial artery in humans.

In this study we investigated whether there exists a periodic contractile activity of the radial artery, and we evaluated the impact of such an oscillatory behavior on the mechanical properties of this medium-sized muscular vessel. The internal diameter of the right radial artery was measured noninvasively in six healthy male volunteers aged 18-42 yr using a high-precision ultrasonic echo-tracking device. Blood pressure was simultaneously recorded on the same side at the middle finger by photoplethysmography. The electrical activity of the heart was monitored during the entire experiment by electrocardiography. The frequency components of the arterial diameter, blood pressure, and heart rate were obtained using spectral analysis. Under resting conditions, the radial arterial diameter exhibited a spontaneous oscillation with a period ranging from 45 to 70 s and an amplitude of 80 +/- 14 microns (+/- SE). No very low-frequency mode (< or = 0.02 Hz) was identified in either heart rate or blood pressure. These diameter oscillations affected the distensibility-pressure curves acquired simultaneously. Thus the 3-4% oscillatory variation in arterial diameter was paralleled by a 1.5- to 2-fold change in distensibility. These low-frequency oscillations of large arteries seem to be mediated by an intrinsic vascular mechanism.

Dynamic non-invasive measurements of arterial diameter and wall thickness.

AIM: Non-invasive measurements of arterial diameter and wall thickness are critical in characterizing the onset and development of vascular disease. A precise dynamic method was proposed and tested for this purpose. DESIGN: A non-invasive method of measuring the variations in diameter and thickness of human arteries throughout the cardiac cycle was developed, using a high-precision ultrasonic echo-tracking system. An adaptive filtering technique was used to suppress artefacts caused by the layered tissue structure of the vessel wall. RESULTS: Based on decorrelation of microstructure noise, this technique improved the detectability of the wall interfaces, which allowed a determination of thickness and diameter. The accuracy and reproducibility of the method were tested by measurements of plastic films with known thicknesses. The discrepancies between standard micrometer and pulse-echo measurement were consistently less than 5 microns for film thicknesses ranging from 220 to 800 microns. The difference between two successive measurements was less than 2 microns. The identity of the measured vascular interfaces was checked in two ways. First, experiments on fixed bovine carotid arteries showed that the identified echogenic interfaces corresponded to the actual anatomical structure, as obtained by acoustic microscopy. Second, the radial artery thickness and diameter were extrapolated to obtain the change in wall volume over one cardiac cycle. The volume was found to be nearly constant, indicating incompressibility. CONCLUSION: This method will make it possible to obtain new information on atherogenesis and other vascular diseases.

Fine-structural study of mitosis in the testacean Arcella vulgaris Ehrbg.

The two nuclei of Arcella vulgaris divide synchronously by closed intranuclear orthomitosis during the formation and deployment of the thecagenous cytoplasmic bud. In prophase, the two nuclei are stacked one behind the other in front of the pseudostome, and markedly flattened, which brings the chromosomes near the equatorial plane. The nucleolus disperses, the nuclear lamina gradually disappears, and non-oriented microtubule bundles grow from intranuclear MTOCs. The condensing chromosomes already show attachment sites for one or more microtubules. In prometaphase, the nuclei are still stacked; the chromosomes further condense, the microtubules are oriented but short, leaving large polar regions of the nucleus filled with diffuse nucleolar material. At metaphase, the nucleus elongates to become spherical to barrelshaped; the spindle microtubules are longer but do not reach the nuclear envelope at the poles. In the polar regions, the nucleolar material aggregates into globular masses. The nuclear envelope remains continuous and devoid of lamina, but becomes sinuous. The kinetochores are improminent, associated with up to 6 microtubules. There are no nuclear pole bodies or extranuclear microtubules. At telophase, the nuclear envelope becomes very convoluted, suggesting that portions of the daughter nuclei bud off into the cytoplasm. Annulate lamellae occur inside the nuclei. The chromosomes decondense and the nuclear lamina is reformed, simultaneously with the appearance of new nucleoli which then fuse into one. Post-telophase nuclei undergo shuttle migrations with the cytoplasm between daughter cells.

New ultrastructural data on the morphogenesis of the test in the testacean Arcella vulgaris.

Transmission electron microscopic studies of dividing Arcella vulgaris Ehrbg. have shown that:

Nuclear fine structure at interphase and during encystment in two forms of the testacean Arcella vulgaris.

Arcella vulgaris and A. vulgaris var. multinucleata have two and seven vesicular nuclei, respectively. In early interphase, the nuclei are spherical, with a main central nucleolus and several small peripheral nucleoli. The main nucleolus has mixed fibrillar and granular components and no apparent chromatin bodies in the nucleolus-organizing regions (NORs). The nuclear chromatin is dispersed except for small heterochromatin lumps. Nuclear bodies of fibrous structure occur outside the main nucleolus. The nuclear envelope shows an internal lamina and an external layer of tangential fibres. In middle interphase, the nuclei become irregular in shape and adjacent to the plasma membrane at the dorsolateral cell surface. The condensation of the chromatin increases. The nucleolus is often eccentric and its NORs show conspicuous bodies of condensed chromatin surrounded by a halo and a fibrous transcription zone. By the end of interphase, the main nucleolus becomes polymorphic and segregated into a fibrillar basal part which contains a vacuolar area with dense inclusions, and a fibro-granular cap which contains many fibrous electron dense bodies. These are likely to be the nuclear chromatin elements. In early resting cysts, the nuclei detach from the cell membrane and approach one another. The main nucleolus segregates into large, mainly peripheral fibrillar blocks inside a granular mass. The NORs consist of condensed chromatin bodies without a transcription zone around them. The nuclear chromatin is condensed. Conspicuous intranuclear annulate lamellae bearing pore complexes occur only in cysts.