Beyond cell replacement: unresolved roles of NG2-expressing progenitors

Abstract

NG2-expressing parenchymal precursors (NG2+p) serve as primary source of myelinating oligodendrocytes in both the developing and adult Central Nervous System (CNS). However, their abundance, limited differentiation potential at adult stages along with stereotypic reaction to injury independent of the extent of myelin loss suggest that NG2+p exert functions additional to myelin production. In support of this view, NG2+p express a complex battery of molecules known to exert neuromodulatory and neuroprotective functions. Further, they establish intimate physical associations with the other CNS cell types, receive functional synaptic contacts and possess ion channels apt to constantly sense the electrical activity of surrounding neurons. These latter features could endow NG2+p with the capability to affect neuronal functions with potential homeostatic outcomes. Here we summarize and discuss current evidence favoring the view that NG2+p can participate in circuit formation, modulate neuronal activity and survival in the healthy and injured CNS, and propose perspectives for studies that may complete our understanding of NG2+p roles in physiology and pathology.

Keywords: buffering; depolarization; myelin; neuromodulation; neuroprotection.

Figure 1

NG2+p distribution in the adult cerebellum. (A,A′) Two weeks after tamoxifen induction, multiprocessed cells identified by NG2 (red), and YFP (green) expression appear closely associated to calbindin+ (blue) Purkinje cells in adult NG2CreER™; R26YFP mouse cerebellum. NG2+p arborizations envelop Purkinje cell somata and dendrites [arrowheads in (A,A′)]. (A) Confocal stack comprising 20 optical section 1 mm thick. (A′) Single confocal plane. Scale bars: 10 μm.