Most of the known bactericidal properties of the lungs reside in the phagocytic and lyric potential of the alveolar macrophages (1, 2). Besides maintaining the sterility of the alveolar surface, alveolar macrophages also participate in the clearance of dust and debris from the nonciliated portions of the lung (3, 4). As these important roles of the alveolar macrophage were recognized, m a n y investigators a t t e m p t e d to determine the origin of the cells (reviewed in Bertalanffy [5,6]).Several different cells have been suggested as the progenitor of the alveolar macrophage; the sources of macrophages most frequently mentioned have been hematopoietic tissues (7,8) and intrapulmonary tissues (9, 10). Recently, t'inkett et al. (11) utilized mouse irradiation chimeras in which donor hematopoiefic cells were marked by the T8 chromosome and concluded that two-thirds of alveolar macrophages were of hematopoiefic origin. Virolainen (12) applied the T6 method to organ culture and concluded that all dividing free cells were of hematopoietic origin. Unfortunately, the use of a chromosomal marker visible only during mitosis limited these studies to dividing cells and did not permit morphologic evaluation of these cells. Brunstetter et al. (13), using reciprocal chimeras in which donor hematopoietic cells either carried or lacked an identifiable esterase marker, concluded that alveolar macrophages were primarily of bone marrow origin. However, their analytical method was qualitative and necessitated the pooling of all free cells recovered in the lung washing.In view of these conflicting reports, it was apparent that the experimental approach to this problem must include: (a) a specific marker to identify the origin of individual alveolar macrophages, (b) the utilization of an unselected or randomly selected popu-* This paper has been presented in part at the