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Belaid, N.

Publications and source records attributed to Belaid, N..

2 recordsLinked to original sources

Sterols regulate ciliary membrane dynamics and hedgehog signaling in health and disease

The primary cilium is a specialized signaling hub whose function depends on a tightly regulated membrane composition. While its protein content is well-characterized, its lipid identity, particularly regarding sterols, remains poorly defined. Here, we used mass spectrometry-based lipidomics to map the sterol profile of isolated primary cilia from MDCK cells. We found that ciliary membranes are enriched in cholesterol and desmosterol while excluding precursors like 7-lathosterol and limiting others, suggesting a selective sterol barrier. Inhibiting cholesterol biosynthesis at distinct enzymatic steps led to sterol accumulation, altered ciliary membrane fluidity, and impaired Hedgehog signaling, including defective Smoothened (Smo) retention-- even in the presence of a constitutively active form of Smo. These findings link sterol homeostasis to ciliary membrane properties and signaling fidelity. Our work provides a molecular framework for understanding Hedgehog-related phenotypes in disorders like Smith-Lemli-Opitz Syndrome, highlighting the importance of membrane lipid composition in developmental signaling.

cell biology↗

BCL-xL antagonizes the deleterious effects of KRAS on mitochondrial scaffolding

In addition to its canonical role as a regulator of mitochondrial outer membrane permeabilization, BCL-xL exerts diverse non canonical functions contributing to cancer cell aggressiveness. In particular it regulates KRAS intracellular activation levels. We herein explored the mechanistic basis for this effect by a spatially restricted biotin-labelling proteomic approach designed to characterize proteins whose proximity to KRAS, used as a bait, is BCL-xL dependant. BCL-xL loss relocalizes KRAS to the vicinity of mitochondrial proteins. Proximal proteins include the mitochondrial scaffold prohibitin 2 (PHB2), which also interacts with BCL-xL and the downregulation of which prevents BCL-xL sensitive effects of KRAS induced contacts between mitochondria and endosomes, and mitochondrial mass decrease. These results argue that BCL-xL prevents a negative feedback regulation of KRAS canonical signaling by KRAS interference with mitochondrial quality control.

cell biology↗