Smooth Muscle Cell Klf4 Expression Is Not Required for Phenotype Modulation or Aneurysm Formation in Marfan Syndrome Mice—Brief Report

• DOI: 10.1161/atvbaha.122.318509
• Publication Date: 2023-04-27T09:02:00Z
• Authors: Albert J. Pedroza; Alex R. Dalal; Rohan Shad; Nobu Yokoyama; Ken Nakamura; Olivia Mitchel; Casey Gilles; William Hiesinger; Michael P. Fischbein
• Keywords: Mice; Phenotype; Myocytes, Smooth Muscle; Animals; RNA; Cytokines; Aneurysm; Marfan Syndrome

Background:

Smooth muscle cell (SMC) phenotypic reprogramming toward a mixed synthetic-proteolytic state is a central feature of aortic root aneurysm in Marfan syndrome (MFS). Previous work identified Klf4 as a potential mediator of SMC plasticity in MFS.

Methods:

MFS ( Fbn1

C1041G/+

) mouse strains with an inducible vascular SMC fluorescent reporter ( MFS

SMC

) with or without SMC-specific deletion of Klf4 exons 2 to 3 ( MFS

SMC-Klf4Δ

) were generated. Simultaneous SMC tracing and Klf4 loss-of-function ( Klf4Δ mice) was induced at 6 weeks of age. Aneurysm growth was assessed via serial echocardiography (4–24 weeks). Twenty-four-week-old mice were assessed via histology, RNA in situ hybridization, and aortic single-cell RNA sequencing.

Results:

MFS mice demonstrated progressive aortic root dilatation compared with control (WT SMC ) mice regardless of Klf4 genotype ( P <0.001), but there was no difference in aneurysm growth in MFS

SMC-Klf4Δ

versus MFS

SMC

( P =0.884). Efficient SMC Klf4 deletion was confirmed via lineage-stratified genotyping, RNA in situ hybridization, and immunohistochemistry. Single-cell RNA sequencing of traced SMCs revealed a highly similar pattern of phenotype modulation marked by loss of contractile markers (eg, Myh11, Cnn1 ) and heightened expression of matrix genes (eg, Col1a1, Fn1 ) between Klf4 genotypes. Pseudotemporal quantitation of SMC dedifferentiation confirmed that Klf4 deletion did not alter the global extent of phenotype modulation, but reduced expression of 23 genes during this phenotype transition in MFS

SMC-Klf4Δ

mice, including multiple chondrogenic genes expressed by only the most severely dedifferentiated SMCs (eg, Cytl1, Tnfrsf11b ).

Conclusions:

Klf4 is not required to initiate SMC phenotype modulation in MFS aneurysm but may exert regulatory control over chondrogenic genes expressed in highly dedifferentiated SMCs.