Search bioRxiv⌕ Search

Biology subjects

Na, W.

Publications and source records attributed to Na, W..

2 recordsLinked to original sources

Egocentric spatial scaffolds organize cortical memory engrams

Episodic memory requires reconstructing the position of the self within a remembered environment, yet whether and how memory engrams incorporate self-referenced spatial information remains unknown. Using activity-dependent engram tagging, longitudinal calcium imaging and optogenetic perturbation in the retrosplenial cortex, we found that cortical memory engrams are enriched for egocentric and boundary-coding neurons that encode self-position relative to environmental boundaries. Longitudinal imaging revealed that future engram neurons are preferentially recruited from a pre-existing spatial scaffold rather than generated de novo during learning. During memory retrieval, scaffold populations underwent coordinated refinement and became transiently reorganized into a scaffold-engram network state whose dynamics tracked memory expression. Silencing scaffold neurons reduced memory expression while preserving recall dynamics, whereas engram silencing abolished recall dynamics while maintaining a stable low-memory state. Together, these findings identify a scaffold-engram architecture through which episodic memories are reconstructed by reinstating the self-referenced spatial representations within remembered space.

neuroscience↗

Retinoblastoma 1 (RB1) modulates the proliferation of chicken preadipocytes

Retinoblastoma 1 (RB1) has been extensively studied in mammalian species, but its function in avian species is unclear. The objective of this study was to reveal the role of chicken RB1 (Gallus gallus RB1, gRB1) in the proliferation of preadipocytes. In the current study, quantitative real-time PCR analysis showed that the expression levels of gRB1 transiently increased during the proliferation of preadipocytes. The MTT assay showed that gRB1 overexpression suppressed preadipocyte proliferation, and gRB1 interference promoted preadipocyte proliferation. Additionally, cell-cycle analysis indicated that gRB1 may play a crucial role in the G1/S transition. Consistently, gene expression analysis showed that gRB1 knockdown promoted marker of proliferation Ki-67 (MKi67) expression at 96 h (P < 0.05), and that overexpression of gRB1 reduced MKi67 expression at 72 h (P < 0.05). Together, our study demonstrated that gRB1 inhibited preadipocyte proliferation at least in part by inhibiting the G1 to S phase transition.

genetics↗