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  • Title: Differentiation of Acmaea digitalis oocytes with special reference to lipid-endoplasmic reticulum-annulate lamellae-polyribosome relationships.
    Author: Kessel RG.
    Journal: J Morphol; 1982 Feb; 171(2):225-243. PubMed ID: 30086608.
    Abstract:
    During initial stages of oogenesis, many nucleoli are adpressed to the inner membrane of the nuclear envelope. Small nucleolar fragments appear to traverse the pores of the nuclear envelope and accumulate in the perinuclear ooplasm as fibrogranular bodies. Mitochondria become closely associated with some of the fibrogranular bodies. In addition to ribosomes and polyribosomes that are present in small oocytes, lamellae of rough-surfaced endoplasmic reticulum (rER) increase greatly in number during early stages of differentiation. Some individual lamellae are attached at their ends to the outer membrane of the nuclear envelope. Many parallel lamellae of rER are then encountered as well as numerous circular profiles consisting of concentric loops of rER. Soon after the differentiation of the extensive system of rER, lipid droplets or spheres appear in the ooplasm and they are initially surrounded by many circular, concentric lamellae of rER. Initially, the number of concentric lamellae of rER surrounding a lipid droplet may vary from less than a dozen to more than two dozen. During middle and late phases of vitellogenesis, most of the lipid spheres that comprise the most numerous and significant component of the yolk are surrounded by only one or two concentric lamellae of rER (in some cases the lamellae are part rough-surfaced and part smooth-surfaced). In addition, annulate lamellae are then observed to be associated with a portion of the lipid droplet surface. The number of annulate lamellae that extend focally from the lipid sphere distally into the cytoplasm is variable; often two or three to more than a dozen lamellae. Small granules, many of which range from 6 to 12 nm and thin fibrils (approximately 2-3 nm in width) may be associated with the annulate lamellae. In addition, polyribosomes frequently appear to be continuous with the pore-associated material of the annulate lamellae. The ends of some annulate lamellae may extend as lamellae of the rER. The morphologic relationships and relationships and variations observed between the lipid droplets, rER, annulate lamellae, and polyribosomes during lipidogenesis in this oocyte are interpreted to support a recent hypothesis (Kessel, 1981a,b) that the pores of annulate lamellae may be involved in some manner with the processing of ribosomal subunits or precursors into functioning polyribosomes, and that their appearance in specific association with the surface of many lipid spheres and rER in the oocyte late in vitellogenesis may be related to the formation of additional functional polyribosomes necessary to complete the final synthesis of many lipid droplets that are present in the ooplasm of the full-grown oocyte.
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