Functions for platelet factor 4 (PF4/CXCL4) and its receptors in fibroblast-myofibroblast transition and fibrotic failure of arteriovenous fistulas (AVFs)

Yuxuan Xiao; Laisel Martinez; Zachary Zigmond; Daniel Woltmann; Diane V Singer; Harold A Singer; Roberto I Vazquez-Padron; Loay H Salman

doi:10.1177/11297298231192386

Functions for platelet factor 4 (PF4/CXCL4) and its receptors in fibroblast-myofibroblast transition and fibrotic failure of arteriovenous fistulas (AVFs)

J Vasc Access. 2023 Aug 17:11297298231192386. doi: 10.1177/11297298231192386. Online ahead of print.

Authors

Yuxuan Xiao¹, Laisel Martinez², Zachary Zigmond², Daniel Woltmann¹, Diane V Singer¹, Harold A Singer¹, Roberto I Vazquez-Padron², Loay H Salman^{1

3}

Affiliations

¹ Department of Molecular & Cellular Physiology, Albany Medical College, Albany, NY, USA.
² DeWitt Daughtry Family Department of Surgery, Leonard M. Miller School of Medicine, University of Miami, Miami, FL, USA.
³ Division of Nephrology & Hypertension, Albany Medical College, Albany, NY, USA.

PMID: 37589266
PMCID: PMC10998683 (available on 2025-02-17)
DOI: 10.1177/11297298231192386

Abstract

Background: Over 60% of End Stage Renal Disease (ESRD) patients are relying on hemodialysis (HD) to survive, and the arteriovenous fistula (AVF) is the preferred vascular access method for HD. However approximately half of all newly created AVF fail to mature and cannot be used without a salvage procedure. We have recently demonstrated an association between AVF maturation failure and post-operative fibrosis, while our RNA-seq study also revealed that veins that ultimately failed during AVF maturation had elevated levels of platelet factor 4 (PF4/CXCL4). However, a link between these two findings was yet to be established.

Methods: In this study, we investigated potential mechanisms between PF4 levels and fibrotic remodeling in veins. We compared the local expression of PF4 and fibrosis marker integrin β₆ (ITGB6) in veins that successfully underwent maturation with that in veins that ultimately failed to mature. We also measured the changes of expression level of α-smooth muscle actin (αSMA/ACTA2) and collagen (Col1/COL1A1) in venous fibroblasts upon various treatments, such as PF4 pharmacological treatment, alteration of PF4 expression, and blocking of PF4 receptors.

Results: We found that PF4 is expressed in veins and co-localizes with αSMA. In venous fibroblasts, PF4 stimulates expression of αSMA and Col1 via different pathways. The former requires integrins α_vβ₅ and α₅β₁, while chemokine receptor CXCR3 is needed for the latter. Interestingly, we also discovered that the expression of PF4 is associated with that of ITGB6, the β subunit of integrin α_vβ₆. This integrin is critical for the activation of the major fibrosis factor TGFβ, and overexpression of PF4 promotes activation of the TGFβ pathway.

Conclusions: These results indicate that upregulation of PF4 may cause venous fibrosis both directly by stimulating fibroblast differentiation and expression of extracellular matrix (ECM) molecules and indirectly by facilitating the activation of the TGFβ pathway.

Keywords: AVF; ITGB6; PF4; TGFβ pathway; differentiation; fibroblast; fibrosis.

Abstract

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