Electrophysiological properties of rat retinal Muller (glial) cells in postnatally developing and in pathologically altered retinae

Retinal glial Muller cells are characterized by dominant K+ conductances. T he cells may undergo changes of their membrane currents during ontogeny and gliosis as described in rabbit and man. Although the rat retina is often u sed in physiological experiments, the electrophysiology of rat Muller cells is less well studied. The aim of the present study was to characterize the ir membrane currents in postnatal development and in two models of retinal degeneration. Freshly isolated cells were subjected to whole-cell patch cla mp recordings. During the first 4 weeks after birth of rats, their Muller c ells displayed an increase in all membrane currents, particularly in the in ward currents elicited at hyperpolarizing potentials. The decrease of the m embrane resistance from more than 760 M Omega to less than 50 M Omega was a ccompanied by a shift of the zero current potential from about -20 mV to -8 0 mV, similar as earlier observed in developing rabbit Muller cells. These developmental changes were found in pigmented Brown Norway rats as well as in rats with inherited retinal dystrophy (RCS rats). Moreover, an infection of Lewis rats with the Borna disease virus caused substantial neuroretinal degeneration but did not result in a strong reduction of inward currents a nd of the zero current potential of the Muller cells. Thus, rat Muller cell s fail to change their basic membrane properties in two different models of retinal pathology. This is in contrast to human and rabbit Muller cells, w hich have been shown to undergo dramatic changes of their membrane physiolo gy in response to retinal diseases and injuries. GLIA 34: 190-199, 2001. (C ) 2001 Wiley-Liss, Inc.