Establishment and Use of Primary Cultured Astrocytes from Alexander Disease Model Mice.

Abstract

Alexander disease (AxD) is an intractable neurodegenerative disease caused by mutations in(), which is predominantly expressed in astrocytes. Thus, AxD is a primary astrocyte disease. However, it remains unclear howmutations affect astrocytes and cause AxD pathology. Three features are characteristic of AxD astrocytes: (1) Rosenthal fibers (RFs), the hallmark of AxD; (2) aberrant Casignals (AxCa); and (3) upregulation of disease-associated genes (AxGen). We established a primary culture system for astrocytes from an AxD transgenic mouse model, and used it to analyze the above features of AxD pathogenesis in astrocytes. We observed the formation of RFs in AxD primary cultures. The abundance of RFs was greater in AxD-transgene-homozygous compared with -hemizygous astrocytes, indicating a gene dosage effect, and this abundance increased with time in culture, indicating a developmental process effect. However, cultured AxD astrocytes did not exhibit changes in either AxCa or AxGen. We therefore conclude that RFs in astrocytes form via a cell-autonomous mechanism, whereas AxCa and AxGen are likely to occur via a non-cell-autonomous mechanism through interactions with other cells, such as neurons, microglia, and vascular cells. Although primary cultured AxD astrocytes are suitable for elucidating the mechanisms of RFs formation and for intervention studies, it should be noted that they cannot reflect the pathophysiology of non-cell-autonomous events in astrocytes.