Ultrastructural changes that occur in follicular cells of the bat thyroid gland just prior to, and immediately after arousal from hibernation are discussed in relation to the known changes which occur in thyroid function during arousal from hibernation. The most distinctive ultrastructural change that takes place just before emergence from hibernation is the occurrence, extracellularly, of concentrations of small vesicles lying in the colloid near the cell's apical plasma membrane. Similar accumulations of vesicles are absent in the apical cytoplasm of the follicular cell. Other principal changes from the early hibernating state found at this time are an increase in the number of apical vacuoles, dense granules and multivesicular bodies. These changes are followed at arousal itself by the appearance of large numbers of intracytoplasmic colloid droplets, often intimately associated with dense granules. An unusual feature of these follicular cells is that although they are rich in colloid droplets, apical pseudopods cannot be found.Numerous studies have demonstrated that the thyroid gland of mammalian hibernators exhibits an endogenous yearly cycle of activity. The thyroid is most active during the spring, when the animals are emerging from hibernation, and least active during the winter when the animals are hibernating (Kayser, '61; Hoffman, '65). In order to correlate these seasonal changes in thyroidal activity with the ultrastructure of the gland, we have periodically examined the fine structure of the bat follicular cells during the animals' yearly life cycle. In preceding papers we have already described the ultrastructural changes which occur in bat follicular cells during the homeothermic (active), preparatory and hibernating phases of the annual life cycle (Nunez and Becker, '70; Nunez, '71). In this study we describe the changes in follicular cells of the bat just prior to, and during arousal from hibernation.
MATERIALS AND METHODSAdult bats of the species Myotis lucifzigzis and Pipestrilliis pipestrillus were used. All animals were captured in their natural habitat. Hibernating bats were collected in a cave in mid-April near the end of their period of hibernation. Active bats were caught in a barn in late April and in early June. The hibernating and active bats were of either sex. Hibernating animals were gently placed, in the cave where they were collected, into containers, the bottom halves of which were filled with ice in order to maintain the hibernating state. They were taken to the laboratory and kept in a cold room at 4°C. Three of the hibernating bats were killed by rapid decapitation in the cold room the following morning. The other animals were kept at 4°C in the hibernating state and killed 24, 48 and 96 hours later. Active bats were kept in the laboratory at room temperature and killed the following day. For electron microscopy, thyroid glands were removed in toto, and fixed in ice-cold 6.25% glutaraldehyde in 0.067 M cacodylate buffer, pH 7.3, for 4 hours. Next, the tissues were w...