Abstract

Objective: To identify the significance of autophagy in lupus nephritis (LN). Methods: The number of autophagosomes in podocytes was counted and the expression of multiple molecular markers associated with autophagy was evaluated in LN specimens: in renal biopsy specimens from 90 patients with LN and 15 healthy controls, autophagosomes in podocytes were counted using transmission electron microscopy and the expression levels of four autophage related proteins including Beclin-1, microtubule-associated protein light chain 3 (LC3), autophagy-related gene 7 (Atg7), and UNC-51-like kinase 1 (ULK1) were measured using immunohistochemistry. Results: The number of autophagosomes in patients with LN types III, IV, and combined V–IV type were significantly higher than in controls (p < 0.0001; p < 0.0001; p = 0.009, respectively). However, the autophagosomes numbers in patients with II and V types LN were significantly lower than controls (both p < 0.0001). Various levels of marker expression were identified, and they correlated significantly with LN pathology classifications. Moreover, the percentage of marker expression in LN types III, IV and V-IV were significantly higher than controls (p < 0.05), while that in types II and V were lower than controls, although the difference for LC3 and ULK1 was not statistically significant. Conclusions: Autophagy activity and expression pattern of autophagy-related markers in podocytes were significantly positively correlated with LN of types III, IV, and V–IV, but negatively correlated with II and V types. Therefore autophagy could be a useful predictor of LN pathology type, and be informative and helpful in the development of treatment strategies in clinical settings.

Highlights

  • Lupus nephritis (LN) is one of the most common characteristics observed in patients with systemic lupus erythomatosus (SLE)

  • Several lines of evidence have confirmed the role of podocyte injury in the pathogenesis of LN [3,4]

  • The clinical manifestations of LN of different types were summarized in Tables 2 and 3

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Summary

Introduction

Lupus nephritis (LN) is one of the most common characteristics observed in patients with systemic lupus erythomatosus (SLE). The different renal patterns of injury, including mesangial, endothelial, epithelial (podocyte), tubulointerstitial and vascular involvement, have been associated with different pathogeneses, clinical presentations, therapeutic responses and outcomes in LN patients [1]. Podocytes are highly specialized epithelial cells which line the urinary surface of the glomerular capillary tuft in the kidney, and are involved in the ultrafiltration of blood. Several lines of evidence have confirmed the role of podocyte injury in the pathogenesis of LN [3,4]. Chronic damaging stimuli, such as infection, metabolic factors, and haemodynamic abnormalities, can induce oxidative stress in podocytes, leading to the foot-process effacement of podocytes and eventually the loss of podocytes. Prolonged podocyte injury further leads to glomerulosclerosis and the progression of kidney disease [5]

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