Isotretinoin improves tendon-bone interface healing and inhibits muscle-fatty infiltration through GATA6 activation in a rat model of rotator cuff repair.

BACKGROUND

Rotator cuff (RC) repair often fails due to poor healing at the tendon-to-bone interface (TBI) and irreversible fatty infiltration (FI) of the muscle. GATA6 has emerged as a potential transcriptional regulator of tissue regeneration, but no therapeutic agents currently target this pathway.

PURPOSE: To evaluate the therapeutic potential of isotretinoin, a known GATA6 modulator, in enhancing TBI healing and reducing FI following RC repair in a rat model.

METHODS

An RC repair rat model was established using 12-week-old male Sprague-Dawley rats. In the isotretinoin group, 10 rats received an oral dose of 7 mg/kg isotretinoin daily for 6 weeks following RC tendon transection, while the control group of 10 rats received only 0.9% saline. All rats were euthanized 6 weeks postsurgery. FI in the supraspinatus tendon was assessed qualitatively and quantitatively. TBI healing was histologically evaluated using the Bonar score after general tissue staining. Additionally, a biomechanical assessment of TBI healing was conducted utilizing a universal testing machine.

RESULTS

Isotretinoin treatment significantly upregulated Gata6 expression while downregulating Caveolin-1 and PPAR-γ, with no significant change in C/EBP-α expression. Activation of the PKA/CREB signaling pathway was confirmed by increased phosphorylation of PKA and CREB. Histological analysis demonstrated improved collagen organization and cellularity at the TBI. Biomechanical testing revealed greater tensile strength and stiffness in the isotretinoin group compared to controls. Fatty infiltration in the supraspinatus muscle was markedly reduced.

CONCLUSIONS

Isotretinoin promotes TBI healing and suppresses muscle-FI following RC repair, which is associated with activation of the GATA6-Caveolin-1-PKA/CREB signaling axis.