Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.05.26.656095

Actin Networking Collapse Under STAT5A Deficiency Drives Mitochondrial Dysfunction and Autocrine IFN-beta Production

Abstract

Coordination between actin cytoskeleton networking and mitochondrial organization and health underpins cellular homeostasis. Here, we found STAT5A to be a pivotal transcription factor that sustains the expression of key actin regulators, including ACTN1. STAT5A, but not STAT5B deficiency dismantles F-actin architecture leading to amorphous cell shape, reduced cellular motility, and corrals mitochondria around the nucleus. This actin networking disruption impairs mitochondrial DRP1 recruitment and dynamic equilibrium, leading to ROS-associated DNA damage and cGAS-STING mediated type I IFN production. Consequently, this establishes a chronically IFN-stimulated state in neighboring cells. Conversely, overexpression of STAT5A increases actin cytoskeleton networking and promotes faster cell motility. Moreover, ectopic expression of ACTN1 in the background of STAT5A-knockout cells is sufficient to restore the actin cytoskeleton organization and mitochondrial network morphology, eliminating DNA damage and IFN-signaling. Giving the importance of actin in cellular homeostasis, our findings place actin abundance, as regulated by the STAT5A-ACTN1 axis as essential for linking cytoskeletal integrity with mitochondrial health, restraining aberrant innate immune activation. Graphic Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=172 SRC="FIGDIR/small/656095v1_ufig1.gif" ALT="Figure 1"> View larger version (43K): org.highwire.dtl.DTLVardef@1cee57aorg.highwire.dtl.DTLVardef@3be0cdorg.highwire.dtl.DTLVardef@123ed52org.highwire.dtl.DTLVardef@1b1bfcc_HPS_FORMAT_FIGEXP M_FIG C_FIG Key pointsSTAT5A deficiency disrupts cytoskeletal integrity via ACTN1 loss. The disrupted actin-cytoskeleton impairs mitochondria organization, causing ROS production and DNA damage. STAT5A knockout activates cGAS-STING signaling and IFN-{beta} production. Restoring ACTN1 rescues cytoskeleton, mitochondrial function, and immune balance.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Sun, B., Krishnamohan, M., Nevo, R., Zoler, E., Geiger, B., Schreiber, G.. 2025-05-28. Actin Networking Collapse Under STAT5A Deficiency Drives Mitochondrial Dysfunction and Autocrine IFN-beta Production. https://doi.org/10.1101/2025.05.26.656095

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

KEEP EXPLORING

Related preprints

Sequence context and partner availability specify divergent cell fates from a single transcription factor

Transcription factors drive the gene regulatory networks that control developmental transitions, yet which of their many targets a cell uses remains unresolved. Expressing Cebp, Cebp{beta} or Cebp{delta} identically, alone or with Oct4, Sox2, Klf4 and cMyc, gave four outcomes: adipocyte from fibroblasts and neural stem cells, trophectoderm from embryonic stem cells, and myeloid from B cells. Raising Cebp levels changed how many sites it reached, not which sequence it read: clustered motifs maintained somatic enhancers, while spillover onto low-copy sites created de novo enhancers carrying composites of Cebp and cell-type-restricted partners. In fibroblasts, Cebp also redistributed Oct4, Sox2 and Klf4 from early targets, blocking iPSC formation. Supplying the predicted partners rewrote the output: Spi1 redirected Cebp into parallel adipogenic and myeloid programs, via a transient PpargCD45 state using separate enhancers for each; TFAP2C abolished adipogenic conversion. Motif density and partner composites therefore assemble a factor's instructive output in the receiving cell.

cell biology↗

High-content screening identifies FDA-approved activators of mitophagy

Mitochondrial diseases are highly heterogeneous disorders caused by defects in oxidative phosphorylation, for which only limited therapeutic options are available. The elimination of dysfunctional mitochondria via mitophagy activation is an attractive strategy to treat several mitochondrial diseases, irrespective of the underlying genetic defect. To identify pharmacological activators of this pathway, we performed a high-content screening of 1,971 FDA-approved compounds using cellular reporters of TFEB nuclear translocation and mitophagy. This screening identified 294 compounds that promoted TFEB translocation, nine of which increased the number of mitolysosomes without compromising cell viability or damaging mitochondria. Among the selected compounds, Meptazinol and Ponatinib emerged as the top-ranked mitophagy inducers in fibroblasts from patients with complex I and IV deficiency, respectively, and were prioritised for further characterisation. However, they did not rescue the bioenergetic defect, suggesting that the stimulation of mitophagy per se is not sufficient to ameliorate the OXPHOS defect in mitochondrial diseases. Overall, our findings establish a scalable platform for the identification of pharmacological activators of TFEB and identify candidate compounds for therapeutic modulation of mitophagy.

cell biology↗

Matrix Gla Protein deficiency reveals a previously unrecognized mucosal calcification in the mouse airways

Tracheal calcification is a common finding that is considered to have limited clinical significance when detected most often in elderly individuals. Despite its frequent occurrence, the cellular and molecular mechanisms at the origin of tracheal calcification remain largely unexplored. In this context, we aimed to characterize the development of tracheal calcification, and to determine the role of matrix Gla protein (MGP), a major inhibitor of ectopic calcification whose genetic or pharmacologic deficiency is associated with premature tracheal calcification in humans. We found that wild-type mice undergo an unexpected early physiologic calcification of the tracheal cartilage rings beginning around one month after birth. This calcification progresses in a dynamic rostro-caudal sequence through a process involving terminal differentiation of tracheal chondrocytes. These findings challenge the prevailing view that tracheal cartilage is a permanent hyaline cartilage and instead reveals an early and highly organized physiologic calcification process. Furthermore, our findings further identify MGP as a key regulator of calcification within the respiratory tract. Indeed, MGP deficiency not only markedly accelerates tracheal cartilage calcification through a similar pattern and mechanism but also induces a previously unrecognized calcification of the tracheal mucosa, a lesion absent in wild-type mice. These alterations could partly explain the respiratory manifestations observed in MGP-deficient patients having Keutel syndrome, which include dyspnea, cough, stridor, and recurrent infections, symptoms previously being mainly attributed to calcification of the tracheal cartilage rings.

cell biology↗