Extensive Endoplasmic Reticulum Research Articles

FINE STRUCTURE STUDIES OF PHLEUM ROOT MERISTEM CELLS. II. MITOTIC ASYMMETRY AND CELLULAR DIFFERENTIATION

Avers, Charlotte J. (Douglass Coll., Rutgers—The State U., New Brunswick, N.J.) Fine structure studies of Phleum root meristem cells. II. Mitotic asymmetry and cellular differentiation. Amer. Jour. Bot. 50(2): 140–148. Illus. 1963.—An electron microscopical study showed that ultrastructural differences distinguished the cell dividing symmetrically from that undergoing asymmetrical division in timothy grass epidermis. The spindle orientation led to cytokinesis which produced either equal‐ or unequal‐sized sister cells, but the mitotic apparatus itself varied in the mitoses. In asymmetrical cells, the basal pole showed more extensive endoplasmic reticulum (ER) polarizations, which intruded into the spindle area during metaphase and anaphase. Such ER polarity was not obvious in symmetrical mitosis or in the apical end of asymmetrically dividing cells. The mitotic sequence is described photographically. Foci of ER were observed as early as prophase in the polar region, and it is suggested that there is a resemblance to astral ray foci seen in prophase of animal cell mitosis. Cell plate formation could be detected in anaphase by accumulations of vesicles and ER fragments along the spindle equator. Phragmosomes apparently were not involved in cell plate formation in Phleum, unlike Allium, cytokinesis. The mitotic asymmetry is discussed as a consequence of an intracellular gradient separate from the intercellular gradient of differentiation along the entire length of growing root tip epidermis.

XII.—Electron Microscopy of the Epithelial Cells of the Mid-gut and Hepatic Cæca of Blatta Orientalis

SynopsisElectron micrographs of the anterior part of the mid-gut and hepatic cæca of Blatta orientalis Linn, show epithelial cells in both secretory and absorptive cycles. The epithelial cells possess microvilli and their lateral margins are provided with irregularly shaped projections that interdigitate with neighbouring cells. Vacuole-like structures were observed in association with the mitochondria of absorptive and degenerating cells. These vacuoles, it is suggested, represent degeneration products. Bundles of saccules and associated groups of vacuoles and vesicles represent the Golgi rods and granules of light microscopy. Epithelial cells engaged in absorption differ from those in which the elaboration of secretion is taking place, in the arrangement of the Golgi saccules and vacuoles, in the size of the Golgi vacuoles, in the distribution of the mitochondria, and in the possession of a less extensive endoplasmic reticulum.

Chondrogenesis, studied with the electron microscope.

The role of the cells in the fabrication of a connective tissue matrix, and the structural modifications which accompany cytodifferentiation have been investigated in developing epiphyseal cartilage of fetal rat by means of electron microscopy. Differentiation of the prechondral mesenchymal cells to chondroblasts is marked by the acquisition of an extensive endoplasmic reticulum, enlargement and concentration of the Golgi apparatus, the appearance of membrane-bounded cytoplasmic inclusions, and the formation of specialized foci of increased density in the cell cortex. These modifications are related to the secretion of the cartilage matrix. The matrix of young hyaline cartilage consists of groups of relatively short, straight, banded collagen fibrils of 10 to 20 mmicro and a dense granular component embedded in an amorphous ground substance of moderate electron density. It is postulated that the first phase of fibrillogenesis takes place at the cell cortex in dense bands or striae within the ectoplasm subjacent to the cell membrane. These can be resolved into sheaves of "primary" fibrils of about 7 to 10 mmicro. They are supposedly shed (by excortication) into the matrix space between the separating chondroblasts, where they may serve as "cores" of the definitive matrix fibrils. The diameter of the fibrils may subsequently increase up to threefold, presumably by incorporation of "soluble" or tropocollagen units from the ground substance. The chondroblast also discharges into the matrix the electrondense amorphous or granular contents of vesicles derived from the Golgi apparatus, and the mixed contents of large vacuoles or blebs bounded by distinctive double membranes. Small vesicles with amorphous homogeneous contents of moderate density are expelled in toto from the chondroblasts. In their subsequent evolution to chondrocytes, both nucleus and cytoplasm of the chondroblasts undergo striking condensation. Those moving toward the osteogenic plate accumulate increasingly large stores of glycogen. In the chondrocyte, the enlarged fused Golgi vesicles with dense contents, massed in the juxtanuclear zone, are the most prominent feature of the cytoplasm. Many of these make their way to the surface to discharge their contents. The hypertrophied chondrocytes of the epiphyseal plate ultimately yield up their entire contents to the matrix.