Table 2.
The double-edged effects of HA in kidney diseases. This table outlines the beneficial and detrimental effects of HMW- and LMW-HA in the various kidney diseases discussed in this review. Here, one can appreciate that HMW-HA lends itself to protective effects, whereas LMW-HA promotes the deleterious characteristics of each disease
Disease | Positive effects of HA | Negative effects of HA |
---|---|---|
Acute kidney injury (AKI) | IL-10-induced HMW-HA reduces fibrosis in I/R model [22] | LMW-HA [46]-CD44 interaction increases the presence of fibrotic molecules (collagen, α-SMA) and causes tubular damage [47] |
Chronic kidney diseases (CKD) | Can potentially serve as a biomarker to distinguish between CKD and AKI in certain clinical cases | Increases pro-fibrotic cells and molecules (macrophage presence, CD44 and LYVE-1 expression, α-SMA levels) [46] |
Diabetic nephropathy | Maintains structure of glomerular endothelium [48]; HMW-HA associated with less CD44-dependent inflammation [49] | Elevated levels associated with disease development [50] |
IgA nephropathy | HA-CD44 interaction plays a role in disease development [51] and fibrotic complications (crescentic glomerulonephritis) [52] | |
Obstructive uropathy | IL-10-induced HMW-HA reduces fibrosis [22] | Acts as nidus for calcium stone formation to cause obstructive disease [53–55] |
Transplant | Can serve as a predictive biomarker for unsuccessful transplant [56] | Associated with organ rejection [57] |
Vesicoureteral reflux | Reduces occurrence of UTIs caused by VUR [58] |