Induced Remodelling of Astrocytes In Vitro and In Vivo by Manipulation of Astrocytic RhoA Activity

Cells. 2023 Jan 15;12(2):331. doi: 10.3390/cells12020331.

Abstract

Structural changes of astrocytes and their perisynaptic processes occur in response to various physiological and pathophysiological stimuli. They are thought to profoundly affect synaptic signalling and neuron-astrocyte communication. Understanding the causal relationship between astrocyte morphology changes and their functional consequences requires experimental tools to selectively manipulate astrocyte morphology. Previous studies indicate that RhoA-related signalling can play a major role in controlling astrocyte morphology, but the direct effect of increased RhoA activity has not been documented in vitro and in vivo. Therefore, we established a viral approach to manipulate astrocytic RhoA activity. We tested if and how overexpression of wild-type RhoA, of a constitutively active RhoA mutant (RhoA-CA), and of a dominant-negative RhoA variant changes the morphology of cultured astrocytes. We found that astrocytic expression of RhoA-CA induced robust cytoskeletal changes and a withdrawal of processes in cultured astrocytes. In contrast, overexpression of other RhoA variants led to more variable changes of astrocyte morphology. These induced morphology changes were reproduced in astrocytes of the hippocampus in vivo. Importantly, astrocytic overexpression of RhoA-CA did not alter the branching pattern of larger GFAP-positive processes of astrocytes. This indicates that a prolonged increase of astrocytic RhoA activity leads to a distinct morphological phenotype in vitro and in vivo, which is characterized by an isolated reduction of fine peripheral astrocyte processes in vivo. At the same time, we identified a promising experimental approach for investigating the functional consequences of astrocyte morphology changes.

Keywords: RhoA; astrocytes; cytoskeleton; morphology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Astrocytes* / metabolism
  • Cytoskeleton
  • Neurons*
  • Signal Transduction

Grants and funding

This work was supported by German Research Foundation (DFG; SFB1089 B03, SPP1757 HE6949/1, HE6949/3, FOR2795 P2 to C.H.; ZE994/2 to A.Z.; SFB1089 to M.K.S.; SFB1089 P02 to S.S.; PO732 to E.P.). Research in the Wachten lab was supported by grants from the DFG (SFB 1454 project number 432325352, TRR83 project number 112927078, SPP1926, SPP1726, FOR2743), under Germany’s Excellence Strategy (EXC2151 project number 390873048).