bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.09.10.750543

Lipopolysaccharide-induced plasma membrane hyperpolarization in Chara corallina and Arabidopsis thaliana: evolutionary conservation of bacterial elicitor perception across the streptophyte lineage

Abstract

The green alga Chara corallina (Charophyceae) is a long-standing model for plant electrophysiology and, owing to its phylogenetic proximity to the ancestors of land plants, an informative system for probing the evolutionary depth of plant-microbe interactions. Bacterial lipopolysaccharide (LPS) is a potent microbe-associated molecular pattern (MAMP) that triggers innate immune signaling in both animals and land plants, but nothing was known about how a charophyte alga responds to this elicitor at the level of the plasma membrane. Here we measured resting membrane potential (Vm) changes in C. corallina internodal cells exposed to purified LPS from three Gram-negative bacteria: Escherichia coli, Pseudomonas aeruginosa, and Pectobacterium carotovorum subsp. carotovorum. All three LPS preparations triggered hyperpolarization of the plasma membrane, but with strikingly different kinetics: E. coli LPS produced a transient hyperpolarization that decayed within minutes, whereas LPS from P. aeruginosa and P. carotovorum produced a sustained, non-transient hyperpolarization that persisted for the duration of recording. Pretreatment with vanadate, a specific inhibitor of P-type H+-ATPases, abolished the electrogenic component of the resting potential and strongly reduced the LPS-induced hyperpolarization, suggesting that the plasma membrane proton pump participates in this response. Strikingly, membrane potential recordings performed in Arabidopsis thaliana cell suspension cultures reproduced chemotype specific kinetic dichotomy: LPS from the non-phytopathogen E. coli and P. aeruginosa, both induced a transient hyperpolarization, whereas LPS from the phytopathogen P. carotovorum subsp. carotovorum induced a non-transient, sustained hyperpolarization of A. thaliana cells. These results demonstrate that Chara possesses an electrophysiologically detectable LPS-sensitive perception system that pre-dates the divergence of land plants, that this system can discriminate between LPS chemotypes with distinct kinetic signatures, and that the same transient/non-transient signature is conserved in A. thaliana. These findings argue that the transient/non-transient dichotomy documented here may reflect an ancestral, broadly conserved capacity to decode structural variation in bacterial glycolipids at the level of the plasma membrane.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Baudin, L., Keller de Schleitheim, T., Bouteau, F.. 2026-09-13. Lipopolysaccharide-induced plasma membrane hyperpolarization in Chara corallina and Arabidopsis thaliana: evolutionary conservation of bacterial elicitor perception across the streptophyte lineage. https://doi.org/10.64898/2026.09.10.750543

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Nucleosome Core Allostery Governs Chromatin Recognition and Cell Fate

Nucleosomes regulate chromatin folding, accessibility, and factor recruitment. Current models primarily attribute these functions to histone tail modifications, while the core is largely viewed as a structural scaffold. Yet subtle changes within the nucleosome core can produce profound functional consequences, and the mechanisms underlying these effects remain unclear. Here, we describe nucleosome core allostery as a fundamental principle of chromatin regulation that amplifies the impact of minimal nucleosome variations. Leveraging natural differences between H2A.Z variants, we show that the nucleosome core encodes distinct conformational dynamics that propagate allosterically, thereby controlling nucleosome accessibility and recognition by chromatin factors. As a result, a single buried amino acid substitution alone is sufficient to reprogram nucleosome dynamics and bias cell identity. Our findings establish the nucleosome core as an allosteric regulatory module and provide a generalizable framework for how subtle variation within nucleosomes is amplified into diverse biological outcomes in development and disease.

cell biology↗

SOX4 Reprograms Adipose Stromal Cells into a Cancer-Associated Fibroblast-like State to Drive Metabolic Disease

Pathogenic adipose tissue remodeling promotes metabolic disease in obesity, but the mechanisms that establish this unhealthy tissue state remain poorly understood. Here, we show that obesity drives SOX4-dependent reprogramming of mesenchymal stromal cells (MSCs) into cancer-associated fibroblast-like (CAF-like) cells that promote adipose tissue dysfunction. TGF{beta} signaling is elevated in obesity and activates SOX4 in mouse and human MSCs, inducing their conversion to a CAF-like state. In mice, MSC-specific SOX4 activation induces the CAF-like program and exacerbates adipose tissue inflammation and glucose intolerance, whereas Sox4 deletion attenuates inflammation and improves glucose homeostasis during obesity. We further identify the growth factor Midkine (MDK) as a SOX4-regulated paracrine effector produced by CAF-like cells. MDK inhibition in obese mice reduces adipose tissue inflammation and improves metabolic function. Together, these findings define a TGF{beta}-SOX4-MDK stromal signaling axis that drives pathological adipose tissue remodeling in obesity and highlight this pathway as a potential therapeutic target for improving metabolic health.

cell biology↗

PDLIM5 Modulates YAP1 Localisation and Fibrogenic Gene Expression in Hepatic Stellate Cells

Hepatic stellate cells (HSCs) are the key cellular drivers of liver fibrosis. During liver injury and chronic inflammation HSCs adopt an activated phenotype and secrete fibrotic extracellular matrix (ECM) components such as collagen 1. Mechanical cues derived from the fibrotic ECM drive and support the activation of HSCs, via mechanisms that involve integrins and the mechano-sensitive transcriptional regulator YAP1. It is not yet well understood how external mechanical cues are translated into a molecular response that alters YAP1 nuclear shuttling. There is evidence that suggests the PDZ and LIM domain protein (PDLIM) 5 can regulate YAP1 shuttling in human epithelial cells. We therefore investigated whether PDLIM5 is expressed in HSCs and contributes to YAP1 associated HSC mechano-activation. PDLIM5 protein was detected in HSCs in fibrotic human and mouse liver. PDLIM5 transcript and protein were expressed by primary human and mouse HSCs and by the immortalised HSC LX-2 cell line. PDLIM5 localised with actin stress fibres suggesting a role in HSC adhesion. Co-immunoprecipitation and proximity ligation in LX-2 cells support an association between PDLIM5 and YAP1. We used pharmacological (paclitaxel) and genetic (siRNA and CRISPRi) approaches to inhibit PDLIM5 in HSCs. Inhibiting PDLIM5 reduced YAP1 nuclear localisation and fibrotic gene (COL1A1, ACTA2) expression in LX-2 cells. Overall, these data support a role for PDLIM5 in regulating YAP1 localisation and fibrogenic gene expression in HSCs.

cell biology↗