A B S T R A C TDifferentiating white adipose tissue from presumptive and developing fat pads of newborn and young rats was fixed in buffered osmium tetroxide, embedded in Vestopal W, and examined in an electron microscope. Pre-adipose cells were found to be fibroblasts characterized by their spindle shape, long tenuous cytoplasmic extensions, and profuse endoplasmic reticulum. The developmental stages traced from fibroblast to mature adipose cell show a gradual change in cell shape, an accumulation of cytoplasm and non-membrane-bounded lipid, a decrease in the endoplasmic reticulum, and a change in shape of mitochondria. Transitory glycogen appears at mid-differentiation. Numerous smooth-membraned vesicles occur in the cytoplasm throughout differentiation. Pinocytosis is constantly evident. Cells of the mnltilocular stage are shown to differ from brown fat ceils, particularly with respect to cytoplasmic membrane systems and mitochondria. No transport of particulate lipid from the lumen of the capillary to, or within, the adipose cell was detected, nor could any cell organelle be demonstrated to be visibly related to lipid synthesis and/or deposition.

This report presents an electron microscope study of white adipose cells depleted of their lipid inclusion by prolonged low food intake. The tissue was fixed in phosphate-buffered 1% osmium tetroxide, embedded in Vestopal W, and sections were stained with lead hydroxide. Such cells differ in shape and size from signet-ring cells. They are ovoid, diminished in size, and the cell surface has become indented in all planes of the cell. The intercellular space is expanded with concentrations of collagen fibers in close association with the cell surface. These changes are presumed to be mechanical events associated with loss of lipid from the cell. Subcellular changes include the appearance of a n extremely large number of pinocytotic vesicles and cytoplasmic vesicles similar in appearance, membrane-bound dense bodies, five-layered membranous structures, vesiculated bodies, and areas of flocculent material. Mitochondria and nuclei appear to be similar to their counterparts in signet-ring cells. Observations are discussed with relation to ultrastructural changes reported in other studies in which adipose cells were depleted of fat by acute starvation or experimental deprivation of insulin. It is suggested that intracellular structural changes are probably associated with adaptive alterations in the metabolism of the cell.

The electron microscopic appearance of glycogen has been studied in the organs of several animal species. Glycogen almost always appears as roughly circular granules from 150 to 400 A in diameter. The intrinsic electron density of glycogen varies from tissue to tissue; however, treatment with lead hydroxide as described by Watson deeply stains the granules. Glycogen pellets were isolated from some of the tissues studied by centrifugation. Such pellets were shown to be glycogen by chemical and histochemical criteria. When thin sections of the pellet are examined under the electron microscope they can be seen to consist of densely packed granules similar to those found in the intact tissues. Such pellets are also stained for electron microscopy by short exposure to lead hydroxide.