Glia of vertebrates and invertebrates alike represents a diverse population of cells, divided into numerous classes with different structural and functional characteristics. In insects, glia fall within three basic classes: (1) surface glia (SG), subdivided into perineurial and subperineurial glia, are located on, and extend processes that envelop, the outer surface of the nervous system; (2) cell body glia (CBG) are located amongst neuronal somata in the outer cell body rind (cortex) and extend processes which encapsulate them; (3) neuropil glia (NPG), subdivided into astrocyte-like and ensheathing glia, exhibit somata located between the cortex and central domains consisting of neuronal processes and synapses (neuropil) and is thus the glial class most closely associated with neurites. With the help of current genetic tools developed in Drosophila it is possible to establish the origin of these glial populations and follow them throughout their migration and differentiation. Differentiated glia of the larva (primary glia) forms largely from a small set of uniquely identifiable progenitors (glioblasts and neuro-glioblasts) located in the embryonic neurectoderm. Differentiated glia of the adult (secondary glia) is formed by different mechanisms depending on the glial class. Primary neuropil glia undergoes programmed cell death during metamorphosis and is replaced by secondary neuropil glia which develop from a new set of larval neuro-glioblasts. By contrast, primary surface and cell body glia likely remains intact from the larval to the adult stage, and some populations (perineurial and cell body glia, specifically) proliferate during the larva to form the secondary, adult populations. Recent lineage tracing studies have also shed light on the developmental relationship between the large and diverse sets of secondary glial progenitors associated with the larval optic lobe and optic stalk, and their progeny in the adult visual system.