Fine structure of the silk spinning system in the caddisworm, Hydatophylax nigrovittatus (Trichoptera: Limnephilidae)

• Published in: Applied microscopy Vol. 50; no. 1; p. 16
• Main Authors: Kim, Hyo-Jeong, Sun, Yan, Moon, Myung-Jin
• Format: Journal Article
• Language: English
• Published: Singapore Springer Singapore 06.08.2020; Springer Nature B.V; SpringerOpen; 한국현미경학회
• Subjects: Aquatic environment; Aquatic insects; Arthropoda; Arthropods; Caddisworm; Cellular manufacture; Chemistry and Materials Science; Fibers; Fine structure; Glycoproteins; Golgi apparatus; Granular materials; Hydatophylax nigrovittatus; Insects; Larvae; Materials Science; Secretory vesicles; Silk; Silk fibroin; Silk gland; Spinning; Terrestrial environments; Ultrastructure; Vesicles; 자연과학일반; Fine structure; Silk; Caddisworm; Hydatophylax nigrovittatus
• ISSN: 2287-4445; 2287-5123; 2287-4445
• DOI: 10.1186/s42649-020-00036-5

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.