Abstract
Examination of large blocks of Epon-embedded, 1.0-μm sections of human embryos and fetuses reveal the presence of hematogenous cells in various stages of differentiation in neural tissue. In every embryo and fetus of 10 weeks ovulation age and younger, hematogenous cells are found randomly scattered in the cerebrum, cerebellum, and spinal cord. Many of these cells appear to undergo spontaneous degeneration in neural tissue and become rarer in older fetuses. Also identified in the neuropil of normal embryos and fetuses are cells with the typical morphological appearance of macrophage containing numerous inclusions of various kinds, both inside and outside the blood vessels. In addition, scattered in the subpial, perivascular, and perineuronal regions of the neural parenchyma are small cells with fusiform nuclei and a small amount of cytoplasm as well as cells with a moderate amount of elongated cytoplasm containing various inclusions and oblong nuclei. All of these cells have clumped heterochromatin along the nuclear membrane which differs from other neuroectodermal cells of the developing human CNS. Although there is no direct evidence to indicate transformation of macrophages to “microglia” or vice versa, the presence of cells having similar nuclear morphology and chromatin pattern while appearing to tbe transitional forms of macrophage, varying from undifferentiated to fully developed, suggest a common lineage of these latter types. It is concluded that migration of hematogenous cells into neural tissue is a ubiquitous developmental phenomenon in young human embryos and fetuses.