Review
Copyright ©The Author(s) 2022.
World J Diabetes. Jul 15, 2022; 13(7): 498-520
Published online Jul 15, 2022. doi: 10.4239/wjd.v13.i7.498
Table 1 Major components of the glomerular basement membrane and the mesangial matrix in normal human glomeruli

Glomerular basement membrane
Mesangial matrix
Heparan sulfate proteoglycanAbundantAbundant
LamininMajor componentMinor component
FibronectinMinor componentMajor component
Type I collagenAbsent in most studiesAbsent in most studies
Type III collagenAbsent in most studiesAbsent in most studies
Type IV collagenMajor componentPresent (inconsistent amounts)
Type V collagenPresentPresent
Type VI collagenPresentPresent
Type XVII collagenPresentUnknown
Type XVIII collagenPresentPresent
Tubulointerstitial nephritis antigen-like-1Low abundanceHigh abundance
Nidogen / EntactinPresentLow abundance
Fibulin-1Present Present
Fibrillin-1Present Present
Nephronectin Present Present
Vitronectin Absent Present
Microfibril-associated proteinsAbsent Present
Table 2 Staining characteristics of the mesangial deposits in diabetic kidney diseases, fibronectin-1 nephropathy, and type III collagen glomerulopathy

Periodic acid Schiff
Methenamine silver
Congo red
Specific analysis
Diabetic kidney diseasePositivePositiveNegativeUnknown material
Fibronectin-1 nephropathyPositiveNegativeNegativeFibronectin-1
Type III collagen nephropathyNegativeNegativeNegativeType III collagen
Table 3 Type IV collagen-related kidney disease

Gene/location
Protein
Mutation
Risk of progression to end-stage kidney disease
X-linked Alport syndromeCOL4A5/X chromosomeα5 chain of type IV collagenHemizygous (males) or heterozygous (females) mutationsHemizygous: 100%; Heterozygous: 25%
Autosomal recessive Alport syndromeCOL4A4 or COL4A3/2q36-37α4 and α3 chains of type IV collagenBiallelic (homozygous or compound heterozygous) mutations100%
Autosomal dominant Alport syndromeCOL4A4 or/COL4A32q36-37α4 and α3 chains of type IV collagenHeterozygous mutations in the α4 or α3 chains20% in patients with risk factors for progression
Digenic Alport syndromeTwo of the COL4A3-5 genesTwo of the α3-5 chains
Table 4 Different composition of glomerular extracellular matrix (glomerular basement membrane and mesangial matrix) in normal subjects and patients with diabetes

Normal glomeruli
Diabetic kidney disease
Heparan sulfate proteoglycansGBM and mesangial matrixDecreased amount
Laminin Predominantly in the GBMInconsistent
Fibronectin-1Mainly in the mesangial matrixIt varies according to DKD stage
Type I collagenInconsistent No detectable
Type III collagenAbsent Abundant
Type IV collagenAbundant in the GBMReduced GBM amount
Type V collagenSimilar to type IV collagenIncreased mesangial amount
Type VI collagenGBM and mesangial matrixIncreased mesangial amount