• Animal cells and systems
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• v.12 no.2
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• pp.109-116
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• 2008

Among the four kinds of silk glands in the funnel-web spider Agelena limbata, the ampullate gland for dragline silk production is the most predominate one in both sexes, and is composed of three functional parts-excretory duct, storage ampulla and convoluted tail regions. Two pairs of major ampullate glands send secretory ductules to the anterior spinnerets, and another two pairs of minor ampullate glands supply the middle spinnerets. There are no apparent differences between the major and minor ampullate glands not only the external spigots but also their internal silk glands. However, the microstructure is very unique in this spider, because each gland has spherical shaped storage sac with twig-like branched tails. Nevertheless, the wall of the secretory region is similarly composed of a single layer of epithelial cells. The mature secretory silks in glandular epithelium are closely packed and accumulated as electron-opaque vesicles. Most of the secretory products which originated from the rough endoplasmic reticula(rER) are grown up by fusion with the surrounding small vesicles however, the Golgi complex does not seem to play an important role in this process of secretion.

• Applied Microscopy
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• v.50
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• pp.16.1-16.11
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• 2020

Silk is produced by a variety of insects, but only silk made by terrestrial arthropods has been examined in detail. To fill the gap, this study was designed to understand the silk spinning system of aquatic insect. The larvae of caddis flies, Hydatophylax nigrovittatus produce silk through a pair of labial silk glands and use raw silk to protect themselves in the aquatic environment. The result of this study clearly shows that although silk fibers are made under aquatic conditions, the cellular silk production system is quite similar to that of terrestrial arthropods. Typically, silk production in caddisworm has been achieved by two independent processes in the silk glands. This includes the synthesis of silk fibroin in the posterior region, the production of adhesive glycoproteins in the anterior region, which are ultimately accumulated into functional silk dope and converted to a silk ribbon coated with gluey substances. At the cellular level, each substance of fibroin and glycoprotein is specifically synthesized at different locations, and then transported from the rough ER to the Golgi apparatus as transport vesicles, respectively. Thereafter, the secretory vesicles gradually increase in size by vesicular fusion, forming larger secretory granules containing specific proteins. It was found that these granules eventually migrate to the apical membrane and are exocytosed into the lumen by a mechanism of merocrine secretion.

• Animal cells and systems
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• v.13 no.2
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• pp.153-160
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• 2009

The fine structural characteristics of the silk spinning apparatus in the titanoecid spiders Nurscia albofasciata have been examined by the field emission scanning electron microscopy (FESEM). This titanoecid spiders have a pair of medially divided cribella just in front of the anterior spinnerets, and the surface of the cribellum is covered by hundred of tiny spigots which produce numerous cribellate silk fibrils. The cribellar silks are produced from the spigots of the sieve-like prate. and considered as a quite different sort of catching silk with dry-adhesive properties. The other types of the silk spigots were identified as follows: ampullate, pyriform and aciniform glands. Two pairs of major ampullate glands send secretory ductules to the anterior spinnerets, and another 1-2 pairs of minor ampullate glands supply the middle spinnerets. In addition, the pyriform glands send ductules to the anterior spinnerets, and two kinds of the aciniform spigots feed silk into the middle (A type) and the posterior spinnerets (both of A & B types), respectively.

• Animal cells and systems
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• v.2 no.1
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• pp.145-152
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• 1998

The spinning apparatus and production of secretory silk from silk gland of the black widow spider, Latrodectus mactans were studied with scanning and transmission electron microscopes. The silk glands were located in seven groups on the spinnerets including each pair of major and minor ampullate, 3 pairs of tubuliform, 1 pair of flagelliform, 2 pairs of aggregate, about 50 pairs of pyriform and over 250 pairs of aciniform glands, respect- ively. Each group of silk gland feeds silk into one of the three spinneret pairs. Secretory silk is synthesized from rough endoplasmic reticulum (rER) of glandular epithelial cells. The secretory silk is transported from toe rER into the secretory vacuoles which are grown up by fusion with the surrounding small vesicles including the secretory silk. The secretory vacuoles, which show a gradual increase in electron density with the process of maturity, are formed without involvement of the Golgi complex, suggesting that they do not play an important role in the processing of the secretory silk. The secretory silk products are released by the mechanism of apocrine secretion, losing part of their cytoplasm. Moreover, another type of silk precursor, possibly protein, appears as granular material, and is also discharged to the luminal cavity.

• Proceedings of the Korean Society of Applied Entomolohy Conference
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• 2001.05a
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• pp.49-49
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• 2001

• Proceedings of the Zoological Society Korea Conference
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• 1996.10a
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• pp.134.2-134
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• 1996

No Abstract, See Full Text

• Applied Microscopy
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• v.33 no.4
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• pp.315-323
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• 2003

The fine structural characteristics of the spinnerets and spigots of the silk producing apparatus in the adult funnel-web spider, Agelena limbata, were analysed with the light and scanning electron microscopes. Silk producing apparatus of this spider was composed of three pairs of spinnerets (anterior, median, posterior) and four different types of spigots-ampullates, tubuliforms, pyriforms and aciniforms. By the examination of their ultrastructural characteristics, it has been revealed that each spigot on the spinnerets are connected through the typical silk gland within abdominal cavity. Among the three pairs of spinnerets, the posterior pairs were highly elongated and has most characteristic features. Two pairs of large ampullates were connected to anterior spinneret and another two pairs of small ampullates to median spinnerets. Spigots of the tubuliforms were observed only in female and were connected both of median and posterior spinnerets respectively. While spigots of the pyriforms were connected on the anterior spinnerets but aciniforms on both of median and posterior spinnerets respectively.

• Applied Microscopy
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• v.42 no.2
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• pp.67-76
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• 2012

The biomimetic approach on the cuticular spinning nozzles of the major ampullate silk glands in the golden-web spider Nephila calvata has been attempted using various visualizing techniques of light and electron microscopes to improve the design of spinning nozzle for producing synthetic nanofibers spun from electrospinning apparatus. The major ampullate spigot which has the most effective nozzle system to produce nanofibers for dragline silk with high strength and elasticity is connected via the bullet type spigot on anterior spinneret with flexible terminal segment. The excretory duct which transports the liquid silk feedstock from ampulla to spigot is divided into 3 limbs by loops back on itself to form an S-shape morphology that is bundled in connective tissue. Final diameter of the nanofibers at nozzle was dramatically reduced by gradual narrowing of duct cuticle less than 10 times comparing to its original size of funnel region. Moreover, the funnel has a characteristic cuticular organization with porous microstructure which seems to be related to water removal from feedstock of silk precursors. High magnification electron micrographs also reveal the presence of the spiral grooves on the surface of the cuticular intima near the valve which presumed to reduce friction during rapid flow of liquid silk.

• Proceedings of the Zoological Society Korea Conference
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• 2000.10a
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• pp.180.2-180
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• 2000

No Abstract, See Full Text

• Proceedings of the Zoological Society Korea Conference
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• 2003.08a
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• pp.156.1-156
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• 2003

No Abstract, See Full Text