Monocarboxylate Transporters: Role and Regulation in Corneal Diabetes

Diabetes mellitus (DM) is a group of metabolic diseases that is known to cause structural and functional ocular complications. In the human cornea, DM-related complications affect the epithelium, stroma, and nerves. Monocarboxylate transporters (MCTs) are a family of proton-linked plasma membrane tr...

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Main Authors: Pawan Shrestha, Amy E. Whelchel, Sarah E. Nicholas, Wentao Liang, Jian-Xing Ma, Dimitrios Karamichos
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Analytical Cellular Pathology
Online Access:http://dx.doi.org/10.1155/2022/6718566
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author Pawan Shrestha
Amy E. Whelchel
Sarah E. Nicholas
Wentao Liang
Jian-Xing Ma
Dimitrios Karamichos
author_facet Pawan Shrestha
Amy E. Whelchel
Sarah E. Nicholas
Wentao Liang
Jian-Xing Ma
Dimitrios Karamichos
author_sort Pawan Shrestha
collection DOAJ
description Diabetes mellitus (DM) is a group of metabolic diseases that is known to cause structural and functional ocular complications. In the human cornea, DM-related complications affect the epithelium, stroma, and nerves. Monocarboxylate transporters (MCTs) are a family of proton-linked plasma membrane transporters that carry monocarboxylates across plasma membranes. In the context of corneal health and disease, their role, presence, and function are largely undetermined and solely focused on the most common MCT isoforms, 1 through 4. In this study, we investigated the regulation of MCT1, 2, 4, 5, 8, and 10, in corneal DM, using established 3D self-assembled extracellular matrix (ECM) in vitro models. Primary stromal corneal fibroblasts were isolated from healthy (HCFs), type I (T1DMs), and type II (T2DMs) DM donors. Monoculture 3D constructs were created by stimulating stromal cells on transwells with stable vitamin C for two or four weeks. Coculture 3D constructs were created by adding SH-SY5Y neurons at two different densities, 12 k and 500 k, on top of the monocultures. Our data showed significant upregulation of MCT1 at 4 weeks for HCF, T1DM, and T2DM monocultures, as well as the 500 k nerve cocultures. MCT8 was significantly upregulated in HCF and T1DM monocultures and all of the 500 k nerve cocultures. Further, MCT10 was only expressed at 4 weeks for all cocultures and was limited to HCFs and T1DMs in monocultures. Immunofluorescence analysis showed cytoplasmic MCT expression for all cell types and significant downregulation of both MCT2 and MCT4 in HCFs, when compared to T1DMs and T2DMs. Herein, we reveal the existence and modulation of MCTs in the human diabetic cornea in vitro. Changes appeared dependent on neuronal density, suggesting that MCTs are very likely critical to the neuronal defects observed in diabetic keratopathy/neuropathy. Further studies are warranted in order to fully delineate the role of MCTs in corneal diabetes.
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spelling doaj-art-5e3b1d32b0544f97af8c6e36a9cac05a2025-02-03T06:04:42ZengWileyAnalytical Cellular Pathology2210-71852022-01-01202210.1155/2022/6718566Monocarboxylate Transporters: Role and Regulation in Corneal DiabetesPawan Shrestha0Amy E. Whelchel1Sarah E. Nicholas2Wentao Liang3Jian-Xing Ma4Dimitrios Karamichos5North Texas Eye Research InstituteDepartment of PhysiologyNorth Texas Eye Research InstituteDepartment of PhysiologyDepartment of BiochemistryNorth Texas Eye Research InstituteDiabetes mellitus (DM) is a group of metabolic diseases that is known to cause structural and functional ocular complications. In the human cornea, DM-related complications affect the epithelium, stroma, and nerves. Monocarboxylate transporters (MCTs) are a family of proton-linked plasma membrane transporters that carry monocarboxylates across plasma membranes. In the context of corneal health and disease, their role, presence, and function are largely undetermined and solely focused on the most common MCT isoforms, 1 through 4. In this study, we investigated the regulation of MCT1, 2, 4, 5, 8, and 10, in corneal DM, using established 3D self-assembled extracellular matrix (ECM) in vitro models. Primary stromal corneal fibroblasts were isolated from healthy (HCFs), type I (T1DMs), and type II (T2DMs) DM donors. Monoculture 3D constructs were created by stimulating stromal cells on transwells with stable vitamin C for two or four weeks. Coculture 3D constructs were created by adding SH-SY5Y neurons at two different densities, 12 k and 500 k, on top of the monocultures. Our data showed significant upregulation of MCT1 at 4 weeks for HCF, T1DM, and T2DM monocultures, as well as the 500 k nerve cocultures. MCT8 was significantly upregulated in HCF and T1DM monocultures and all of the 500 k nerve cocultures. Further, MCT10 was only expressed at 4 weeks for all cocultures and was limited to HCFs and T1DMs in monocultures. Immunofluorescence analysis showed cytoplasmic MCT expression for all cell types and significant downregulation of both MCT2 and MCT4 in HCFs, when compared to T1DMs and T2DMs. Herein, we reveal the existence and modulation of MCTs in the human diabetic cornea in vitro. Changes appeared dependent on neuronal density, suggesting that MCTs are very likely critical to the neuronal defects observed in diabetic keratopathy/neuropathy. Further studies are warranted in order to fully delineate the role of MCTs in corneal diabetes.http://dx.doi.org/10.1155/2022/6718566
spellingShingle Pawan Shrestha
Amy E. Whelchel
Sarah E. Nicholas
Wentao Liang
Jian-Xing Ma
Dimitrios Karamichos
Monocarboxylate Transporters: Role and Regulation in Corneal Diabetes
Analytical Cellular Pathology
title Monocarboxylate Transporters: Role and Regulation in Corneal Diabetes
title_full Monocarboxylate Transporters: Role and Regulation in Corneal Diabetes
title_fullStr Monocarboxylate Transporters: Role and Regulation in Corneal Diabetes
title_full_unstemmed Monocarboxylate Transporters: Role and Regulation in Corneal Diabetes
title_short Monocarboxylate Transporters: Role and Regulation in Corneal Diabetes
title_sort monocarboxylate transporters role and regulation in corneal diabetes
url http://dx.doi.org/10.1155/2022/6718566
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