The essence of multicellular life lies in the dynamic tension between unity and autonomy of individual cells achieved through diverse molecular and structural mechanisms. Plants have evolved plasmodesmata as an elegant solution to this fundamental challenge, creating cytoplasmic bridges that enable both local and systemic communication despite constraints imposed by their rigid cell walls. An emerging paradigm reveals that the core molecular machinery brings about context-dependent, multi-faceted regulation of plasmodesmal permeability through integration with various cellular signaling pathways. In this context, regulation through callose accumulation and degradation has been established as the primary mechanism controlling plasmodesmal permeability. Recent studies now reveal that this regulation is signal-specific and mechanistically diverse, giving rise to the same apparent endpoint of closure with different biological outcomes depending on the signaling context. This creates biological specificity through convergence on shared callose-regulating mechanisms. Understanding how regulatory complexes assemble, achieve signal specificity, and integrate diverse cellular inputs represents a critical frontier in plant biology. In this review, we discuss the molecular players, regulatory mechanisms, and integrative signaling networks that support this paradigm.
Keywords: Callose; cell signaling; cell-to-cell communication; development; immunity; plasmodesmata; plasmodesmata-located proteins.
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