Table 8.
Changes of THP structure in physiology and different pathological conditions
| Different conditions | Structure change in THP molecule |
|---|---|
| Pregnancy | Increased glycosylation |
| Familial juvenile hyperuricemic nephropathy | Mutations in THP genes |
| Autosomal medullary cystic kidney disease 2 | Mutations in THP genes |
| Tubulointerstitial nephritis in SLE | Decease in THP excretion |
| Allograft renal rejection | Reduced mannose residues Reduced Siaα[2,3]Gal/Gal NAc and β[1,4]Glc NAc |
| Glomerulonephritis | Increased IgG, IgM, and IgA depositions in urine casts |
| Interstitial cystitis | Reduced high-molecular weight sialylated oligosaccharides |
| Different urinary diseases | |
| Urinary tract infections, glomerulonephritis, or interstitial nephritis | Decreased N-acetylglucosamine and N-acetylgalactosamine |
| Bartter’s syndrome | Decreased N-acetylglucosamine and less-sialylated chains |
Abbreviation: SLE, systemic lupus erythematosus.