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Results for “Periostracum”

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At least 19 recordsLinked to original sources
PubMed2000

A new model for periostracum and shell formation in Unionidae (Bivalvia, Mollusca).

The periostracum in Unionidae consists of two layers. The outer one is secreted within the periostracal groove, while the inner layer is secreted by the epithelium of the outer mantle fold. The periostracum reaches its maximum thickness at the shell edge, where it reflects onto the shell surface. Biomineralization begins within the inner periostracum as fibrous spheruliths, which grow towards the shell interior, coalesce and compete mutually, originating the aragonitic outer prismatic shell layer. Prisms are fibrous polycrystalline aggregates. Internal growth lines indicate that their growth front is limited by the mantle surface. Transition to nacre is gradual. The first nacreous tablets grow by epitaxy onto the distal ends of prism fibres. Later growth proceeds onto previously deposited tablets. Our model involves two alternative stages. During active shell secretion, the mantle edge extends to fill the extrapallial space and the periostracal conveyor belt switches on, with the consequential secretion of periostracum and shell. During periods of inactivity, only the outer periostracum is secreted; this forms folds at the exit of the periostracal groove, leaving high-rank growth lines. Layers of inner periostracum are added occasionally to the shell interior during prolonged periods of inactivity in which the mantle is retracted.

Animals↗
PubMed2026

The composition of the periostracum in the razor clam Sinonovacula constricta and the mantle's response to sulfide.

The razor clam Sinonovacula constricta inhabits sulfide-rich intertidal sediments and exhibits remarkable tolerance to this toxicant, yet the role of its periostracum in sulfide adaptation remains poorly understood. In this study, we investigated the composition and structure of the periostracum proteins, and the response of the mantle to sulfide stress. Scanning electron microscopy and energy-dispersive X-ray spectroscopy revealed that the periostracum is approximately 10 μm thick and contains 1.43 wt% sulfur, and proteomic analysis further confirmed the presence of organic sulfur (Cys/Met-rich proteins), suggesting its involvement in sulfur deposition. Using LC-MS/MS, we identified 77 high-confidence proteins from the periostracum, which were classified into six functional categories: enzymes, framework proteins, immune-related proteins, calcium ion-related proteins, other proteins, and proteins with unknown functions. Phylogenetic analyses of representative proteins revealed bivalve-specific evolutionary patterns, with several proteins exclusively present in Bivalvia, such as Unknown protein 2 and 7, which possess signal peptides and low-complexity domains. For the sulfide exposure experiment, razor clams were subjected to three Na2S concentrations (0, 10, and 100 μM). qPCR analysis showed that, compared with the control group, Chitin-binding protein 3 and Tyrosinase were significantly upregulated in the mantle, peaking in the 100 μM group at 48 h (5677.84-fold and 157.20-fold, respectively), whereas Collagen and Cadherin 3 were generally suppressed. This study represents one of the most comprehensive proteomic profiles of the razor clam periostracum and highlights the mantle's potential role in sulfide tolerance, offering insights for sulfur-tolerant aquaculture breeding and bioremediation applications.

Animals↗
PubMed1975

An electron microscopic study on the formation of the periostracum in Helisoma (Mollusca).

The ultrastructure of the cells involved in the formation of the periostracum in Helisoma duryi duryi is described. Two distinct types of periostracal cells can be recognized: light and dark. The Golgi complexes of the light cell are involved in the biogenesis of periostracal units which are extruded at the base of the periostracal groove. Here they align into a single row so as to form the membrane-like lamellar covering of the periostracum. While the secretions of the dark periostracal cells contribute to the initial component of the dark layer of the periostracum, the mantle edge gland cells are responsible for its thickening. The adult periostracum is about 2--3 mum thick and it consists of a single dark layer covered by a membrane-like lamellar structure.

Animals↗
PubMed1979

Morphological studies on the periostracum of the fresh-water mussel Amblema (Uniondae): light microscopy, transmission electron microscopy, and scanning electron microscopy.

The structure of the periostracum in the fresh-water mussel Amblema has been described using light microscopy, transmission elec;ron microscopy, and scanning electron microscopy. The structure and evolutive course of the periostracum was studied along its entire length, from the periostracal groove until it forms the tough outer covering of the shell. At least five structurally and functionally distinct regions were identified. In addition, the periostracum itself was seen to be a multilayered structure consisting of three major layers which are themselves subdivided into minor layers. From these morphological observations, a regulatory role for the various periostracal layers in mineral trapping, nucleation, and the subsequent formation of the prismatic and nacreous layers of the shell can be postulated.

Animals↗
PubMed1984

Chitin helicoids accompany protein helicoids in the periostracum of a whelk, Buccinum.

The periostracum of the marine gastropod Buccinum has a helicoidal arrangement of its principal constituent which is a fibrous protein (Hunt and Oates, 1978). Chitin, chemically and physically identified, is present at a concentration of about 6% of the dry weight and can be seen in dispersates of whole periostracum as long fibrils and ribbons between 3 and 14 nm diameter. Deproteinization with hot alkali removes all protein leaving a chitinous 'ghost' of the periostracum. Dispersates, examined negatively stained, show only chitin fibrils and ribbons while sectioned material demonstrates a tenuous, part orthogonal, part helicoidal, architecture based on the chitin residue. The relative roles of the protein and polysaccharide components is speculated upon and comparisons with arthropod cuticle drawn.

Amino Acids↗
PubMed2006

A novel putative tyrosinase involved in periostracum formation from the pearl oyster (Pinctada fucata).

Tyrosinase (monophenol, L-DOPA: oxygen oxidoreductase, EC 1.14.18.1), a kind of copper-containing phenoloxidase, arouses great interests of scientists for its important role in periostracum formation. A cDNA clone encoding a putative tyrosinase, termed OT47 because of its estimated molecular mass of 47kDa, was isolated from the pearl oyster, Pinctada fucata. This novel tyrosinase shares similarity with the cephalopod tyrosinases and other type 3 copper proteins within two conserved copper-binding sites. RT-PCR analysis showed that OT47 mRNA was expressed only in the mantle edge. Further in situ hybridization analysis and tyrosinase activity staining revealed that OT47 was expressed at the outer epithelial cells of the middle fold, different from early histological results in Mercenaria mercenaria, suggesting a different model of periostracum secretion in P. fucata. Taken together, these results suggest that OT47 is most likely involved in periostracum formation. The identification and characterization of oyster tyrosinase also help to further understand the structural and functional properties of molluscan tyrosinase.

Amino Acid Sequence↗
PubMed1976

Ultrastructural studies on the formation of the periostracum in Helix aspersa (Mollusca).

The ultrastructure of the periostracal gland in Helix aspersa and the sequence of formation of the periostracum is described. The periostracal units which measure about 9-12 nm wide and 0.4-0.6 mum long are first detected in the Golgi cisternae. The cisternae containing the unit(s) eventually pinch off from the rest of the Golgi. Microtubules are seen in the space separating the nascent secretory inclusion and the Golgi. Cross-bridges are seen between the microtubules and the secretory inclusions, suggesting that the microtubules are involved in the transport of nascent inclusions away from the site of synthesis. Many periostracal units unite to form periostracal sheets. The mature inclusions containing periostracal sheets migrate to the apical part of the cell where they fuse with the lysosomes before being extruded externally in the lumen of the gland. Perhaps the lysosomal enzymes somehow modify the periostracal units before their extrusion or digest the excess periostracal units. The periostracal sheets released in the lumen disperse randomly to produce a fibrous sheet, which is non-uniform in texture at first but is entirely homogeneous by the time the periostracum is secreted outside.

Animals↗
PubMed1991

Studies on the anticonvulsive, sedative and hypothermic effects of Periostracum Cicadae extracts.

The anticonvulsive, sedative and hypothermic effects of water and ethanol extracts of Periostracum Cicadae (PC), the cast off skin of Cryptotympana atrata were studied. The water-extract of whole Periostracum Cicadae (PCws) had anticonvulsive, sedative and hypothermic effects in rats. Orally, it decreased carrageenin-induced hyperthermia. The hypothermic effect of PCws was potentiated by 5-hydroxytryptophan and antagonized by p-chlorophenylalanine. PCws enhanced the decrease in locomotor activity induced by alpha-methyl-p-tyrosine or 5-hydroxytryptophan and reduced the increase in locomotor activity produced by levodopa plus benserazide or p-chlorophenylalanine. From these results, it was concluded that the sedative and hypothermic effect of PCws may be due to an increase in central serotonergic activity.

Animals↗
PubMed2006

Antioxidant and anti-inflammatory activities of N-acetyldopamine dimers from Periostracum Cicadae.

A known N-acetyldopamine dimer, (2R,3S)-2-(3',4'-dihydroxyphenyl)-3-acetylamino-7-(N-acetyl-2''-aminoethyl)-1,4-benzodioxane (1) and a new N-acetyldopamine dimer, (2R,3S)-2-(3',4'-dihydroxyphenyl)-3-acetylamino-7-(N-acetyl-2''-aminoethylene)-1,4-benzodioxane (2) were isolated from the methanolic extracts of Periostracum Cicadae. Compounds 1 and 2 inhibited the Cu2+ -mediated, 2,2'-azobis(2-amidinopropane) hydrochloride (AAPH)-mediated, and 3-morpholinosydnonimine (SIN)-1-mediated LDL oxidation in the thiobarbituric acid-reactive substances (TBARS) assay. The antioxidant activities of 1 and 2 were tested with respect to other parameters, such as lag time of conjugated diene formation, relative electrophoretic mobility (REM), and apoB-100 fragmentation on copper-mediated LDL-oxidation. Compounds 1 and 2 also showed 1,1-diphenyl-2-picrylhydrasyl (DPPH) radical scavenging activity. Compound 2 was more efficient than compound 1 at inhibiting the reactive oxygen species (ROS) generation, nitric oxide (NO) production, and nuclear factor-kappaB (NF-kappaB) activity as well as the expression of pro-inflammatory molecules such as inducible nitric oxide synthase (iNOS), interleukin (IL)-6, tumor necrosis factor (TNF)-alpha, and cyclooxygenase (COX)-2 in LPS-induced RAW264.7 cells.

Animals↗
PubMed1993

A freshwater bioprobe: Periostracum of the Asian Clam, Corbicula fluminea (Müller) combined with laser microprobe mass spectrometer.

A freshwater bioprobe, combining the Asiatic Clam, Corbicula fluminea (Müller) and the laser microprobe mass spectrometer (LAMMA), can determine anthropogenic chemical contamination of freshwater systems. Laser generated mass spectra from the periostracal layers of clams contaminated with either a salt, potassium bromide, or an aromatic compound, phenol, produce distinctive mass spectral signatures that are different from uncontaminated clams. Uncontaminated clams have characteristic signatures with distinctive spectral peaks less than m/z 41; while exposed clams have many strong peaks well above this m/z. This freshwater bioprobe, using LAMMA to analyze the surface of clams, can be used as a screening tool for monitoring the water-treatment systems, for determining the source of contaminated baseflow and return flow discharge to streams, and for monitoring the water chemistry of a body of water. This system exploits the facility of using the shell instead of soft tissue with the LAMMA and has potential to detect anthropogenically-derived chemical stress.

Journal Article↗