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Published on: October 21, 2022
Compositional differences between infant and adult human corneal basement membranes
Andrea Kabosova1, Dimitri T Azar, Gregory A Bannikov
1Ophthalmology Research Laboratories, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Insights
Corneal basement membranes undergo significant changes during postnatal development, impacting mechanical strength and cell adhesion. These findings offer new insights into corneal maturation and stem cell niches.
Area of Science:
- Ophthalmology
- Developmental Biology
- Biochemistry
Background:
- The distribution of basement membrane (BM) components in adult human corneas is heterogeneous.
- Understanding postnatal corneal development is crucial for comprehending changes in corneal structure and function.
Purpose of the Study:
- To investigate the dynamic changes in epithelial basement membrane (EBM) and Descemet's membrane (DM) components during postnatal corneal development.
- To identify key molecular alterations in corneal BMs from infancy to adulthood.
Main Methods:
- Immunofluorescence analysis of corneal tissues from infants (12 days to 3 years) and adults.
- Antibodies targeting various basement membrane components were utilized to map their distribution.
Main Results:
- Type IV collagen composition in the central EBM shifted post-3 years, with adult limbal BM retaining specific chains.
- Laminin chain distribution varied, with beta2 appearing in limbal BM by age 3 and gamma3 present in all limbal BMs.
- DM composition changed significantly, with certain proteins localizing to the endothelial face in adults and others present on the stromal face in infants.
Conclusions:
- The study describes novel distributions of laminin gamma3, nidogen-2, netrin-4, matrilin-2, and matrilin-4 in the cornea.
- Observed BM component differences correlate with postnatal corneal maturation, potentially influencing mechanical properties, cell adhesion, and differentiation.
Purpose:
Adult human corneal epithelial basement membrane (EBM) and Descemet's membrane (DM) components exhibit heterogeneous distribution. The purpose of the study was to identify changes of these components during postnatal corneal development.
Methods:
Thirty healthy adult corneas and 10 corneas from 12-day- to 3-year-old children were studied by immunofluorescence with antibodies against BM components.
Results:
Type IV collagen composition of infant corneal central EBM over Bowman's layer changed from alpha1-alpha2 to alpha3-alpha4 chains after 3 years of life; in the adult, alpha1-alpha2 chains were retained only in the limbal BM. Laminin alpha2 and beta2 chains were present in the adult limbal BM where epithelial stem cells are located. By 3 years of age, beta2 chain appeared in the limbal BM. In all corneas, limbal BM contained laminin gamma3 chain. In the infant DM, type IV collagen alpha1-alpha6 chains, perlecan, nidogen-1, nidogen-2, and netrin-4 were found on both faces, but they remained only on the endothelial face of the adult DM. The stromal face of the infant but not the adult DM was positive for tenascin-C, fibrillin-1, SPARC, and laminin-332. Type VIII collagen shifted from the endothelial face of infant DM to its stromal face in the adult. Matrilin-4 largely disappeared after the age of 3 years.
Conclusions:
The distribution of laminin gamma3 chain, nidogen-2, netrin-4, matrilin-2, and matrilin-4 is described in the cornea for the first time. The observed differences between adult and infant corneal BMs may relate to changes in their mechanical strength, corneal cell adhesion and differentiation in the process of postnatal corneal maturation.
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