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Acetabulum pedis. Part II: Talocalcaneonavicular joint socket in clubfoot.

Many pathoanatomic studies of clubfeet have been made. Bone changes and ligament and tendon alterations are among the different deformities reported in the literature. The socket of the talocalcaneonavicular joint is termed the acetabulum pedis (AP), and alterations of the joint have been reported previously as malformations associated with clubfoot. We report pathoanatomic observations of AP in three human clubfoot specimens. Anomalies in AP were observed and compared with those in normal feet. In such cases, AP volume is restricted. Surface area is reduced on the acetabular floor and medial wall. Changes occur in the osseous components as well as in the ligaments of the AP.

Cadaver↗

Differential messenger RNA gradients in the unicellular alga Acetabularia acetabulum. Role of the cytoskeleton.

The unicellular green alga Acetabularia acetabulum has proven itself to be a superior model for studies of morphogenesis because of its large size and distinctive polar morphology. The giant cell forms an elongated tube (a stalk of up to 60 mm in length), which at its apical pole makes whorls of hairs, followed by one whorl of gametophores in the shape of a cap. At its basal pole, the cell extends into a rhizoid wherein the single nucleus is positioned. In this study, we have determined the level of specific messenger RNAs in the apical, middle, and basal regions using reverse transcriptase-PCR methodology. Four mRNA classes were distinguished: those that were uniformly distributed (small subunit of Rubisco, actin-1, ADP-glucose, centrin, and alpha- and beta-tubulin), those that expressed apical/basal (calmodulin-4) or basal/apical gradients (calmodulin-2 and a Ran-G protein), and those with development-specific patterns of distribution (mitogen-activated protein kinase, actin-2, and UDP-glucose-epimerase). Restoration of the apical/basal calmodulin-4 mRNA gradient after amputation of the apical region of the cell requires the nucleus and was abolished by cytochalasin D. Accumulation of actin-1 mRNA in the vicinity of the wound set by the amputation needs, likewise, the presence of the nucleus and was also inhibited by cytochalasin. This suggests that actin microfilaments of the cytoskeleton are involved in directed transport and/or anchoring of these mRNAs.

Acetabularia↗

Purification and characterization of a membrane-bound ATPase from Acetabularia cliftonii that corresponds to a Cl(-)-translocating ATPase in Acetabularia acetabulum.

A Mg(2+)-ATPase was solubilized from membranes of Acetabularia cliftonii using nonanoyl-N-methylgluconamide and purified by ion-exchange and gel permeation chromatography. One active ATPase fraction after Mono Q chromatography had a specific activity of 10 units/mg of protein. Judged from subunit composition [54 (a), 50 (b) with a fainter band around 40 kDa], catalytic properties, and N-terminal amino acid sequence of the b subunit, the isolated enzyme was comparable to the Cl(-)-ATPase of Acetabularia acetabulum. Immunological characterization of both subunits showed significant similarity to the F type of ATPase. Cl(-)-transport activity was observed by reconstitution studies into liposomes.

Acetabularia↗

Chloroplast ATPase in Acetabularia acetabulum: purification and characterization of chloroplast F1-ATPase.

ATPases were isolated from chloroplasts of the unicellular marine alga Acetabularia acetabulum. Two preparations of ATPase, a chloroplast-enriched fraction and an alpha beta gamma-complex were compared. The alpha beta gamma-complex was released into an EDTA solution and purified by anion-exchange chromatography, hydrophobic chromatography, and gel permeation chromatography. The subunit composition of this enzyme appeared to be 52-53 (alpha), 51 (beta), and 40 (gamma) kDa from SDS-PAGE. ATPase activity was enriched about 260-fold to a specific activity of approximate 4.1 U.mg protein-1. The catalytic properties of the alpha beta gamma-complex were as follows: pH optimum at 7.5; substrate specificity, ATP > ITP, GTP > UTP = CTP (Km for ATP 0.2 mM); divalent cation requirement, Mg2+ = Mn2+ = Co2+ > Zn2+ > Ni2+ > Ca2+; ATPase activity was inhibited by monovalent anions (NO3-, SCN-), while monovalent cations had neither inhibitory nor stimulatory effect. Orthovanadate had no inhibitory effect on the enzyme activity of alpha beta gamma-complex. Azide was the most effective inhibitor of the alpha beta gamma-complex. N-Terminal amino acid sequences of the alpha and beta subunits were not obtained and appeared to be blocked. The gamma subunit gave a sequence of AGLKEMKD-XIGSVXNTKKI, which showed 60% similarity to the gamma subunits of spinach and Chlamydomonas reinhardtii CF1-ATPase and EF1-ATPase.

Acetabularia↗

Juvenile bone-marrow oedema of the acetabulum treated by iloprost.

The bone-marrow oedema syndrome is associated with local vascular disturbances and may be treated either conservatively or by core decompression after which recovery may take several weeks. We describe a 15-year-old girl with bone-marrow oedema of the left acetabulum which was confirmed by MRI. She presented with a four-week history of severe constant pain. Routine blood tests and plain radiographs were normal. She was treated with intravenous infusions of iloprost on five consecutive days (20 microg administered in 500 ml of sodium chloride). Iloprost causes vasodilatation with reduction of capillary permeability and it inhibits platelet aggregation. She had relief from pain at rest after three days of treatment and was completely free from symptoms after two weeks. MRI after six weeks showed almost complete resolution of the marrow oedema and was normal after four months. This is the first report of the pharmacological treatment of the bone-marrow oedema syndrome in children.

Adolescent↗

Oscillations in ultraweak photon emission of Acetabularia acetabulum (L.).

Ultraweak photon emission of dark-incubated A. acetabulum cells were measured with the use of a sensitive electronphotomultiplier of the Hamamatsu 550 type. The photon count series were subjected to Fourier analysis for 2-1020 sec period range. The average level of photon emission in samples containing 50 cells was approximately. 40% above background. Cell cultures were prepared at least 24 hr before the photon emission measurements and kept un-disturbed ("established cultures"). This paper reports results of Fourier analysis of a number of samples of Acetabularia cells. In a single population cells periodicity of light emission was not defined directly from Fourier transformation. A large number of analyses, however, if they are combined and compared with background data, reveal a cell-culture specific frequency pattern. The results suggest the idea that established cell-cultures are characterized by higher intensities of long period (minutes) oscillations occurs, while a relative decrease was observed in the short period (few seconds) range. The long period oscillations were not detected in cell cultures that were prepared within 1 hr before the photon emission measurements. It is concluded that Fourier analysis of ultraweak photon emission, even with relatively low signals, appears to be possible. It may serve as a non-invasive tool for monitoring the physiological state of cells, or for studying the control of intercellular dynamics.

Acetabularia↗

Acetabulum pedis. Part I: Talocalcaneonavicular joint socket in normal foot.

The socket of the talocalcaneonavicular ball and socket joint in the foot is termed acetabulum pedis (AP). Observations of 72 feet from necropsies of stillborns or deceased newborns are the basis of our architectural description of AP. It has five walls: the roof or superior wall, the floor or inferior wall, the bottom or anterior wall, the medial wall, and the lateral wall. Variations in the tridimensional situation of the anterior and middle articular facets of the calcaneus modify the acetabular floor area. The same is true of the variations in position of the ligaments in both the acetabular floor and the medial wall. These modifications of the acetabular floor and medial wall areas can change the shape of the foot.

Cadaver↗