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      Developmental Expression of Claudins in the Mammary Gland

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          Abstract

          Claudins are a large family of membrane proteins whose classic function is to regulate the permeability of tight junctions in epithelia. They are tetraspanins, with four alpha-helices crossing the membrane, two extracellular loops, a short cytoplasmic N-terminus and a longer and more variable C-terminus. The extracellular ends of the helices are known to undergo side-to-side ( cis) interactions that allow the formation of claudin polymers in the plane of the membrane. The extracellular loops also engage in head-to-head ( trans) interactions thought to mediate the formation of tight junctions. However, claudins are also present in intracellular structures, thought to be vesicles, with less well-characterized functions. Here, we briefly review our current understanding of claudin structure and function followed by an examination of changes in claudin mRNA and protein expression and localization through mammary gland development. Claudins-1, 3, 4, 7, and 8 are the five most prominent members of the claudin family in the mouse mammary gland, with varied abundance and intracellular localization during the different stages of post-pubertal development. Claudin-1 is clearly localized to tight junctions in mammary ducts in non-pregnant non-lactating animals. Cytoplasmic puncta that stain for claudin-7 are present throughout development. During pregnancy claudin-3 is localized both to the tight junction and basolaterally while claudin-4 is found only in sparse puncta. In the lactating mouse both claudin-3 and claudin-8 are localized at the tight junction where they may be important in forming the paracellular barrier. At involution and under challenge by lipopolysaccharide claudins −1, −3, and −4 are significantly upregulated. Claudin-3 is still colocalized with tight junction molecules but is also distributed through the cytoplasm as is claudin-4. These largely descriptive data provide the essential framework for future mechanistic studies of the function and regulation of mammary epithelial cell claudins.

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          The online version of this article (doi:10.1007/s10911-017-9379-6) contains supplementary material, which is available to authorized users.

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          Most cited references75

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          Claudin-1 and -2: Novel Integral Membrane Proteins Localizing at Tight Junctions with No Sequence Similarity to Occludin

          Occludin is the only known integral membrane protein localizing at tight junctions (TJ), but recent targeted disruption analysis of the occludin gene indicated the existence of as yet unidentified integral membrane proteins in TJ. We therefore re-examined the isolated junction fraction from chicken liver, from which occludin was first identified. Among numerous components of this fraction, only a broad silver-stained band ∼22 kD was detected with the occludin band through 4 M guanidine-HCl extraction as well as sonication followed by stepwise sucrose density gradient centrifugation. Two distinct peptide sequences were obtained from the lower and upper halves of the broad band, and similarity searches of databases allowed us to isolate two full-length cDNAs encoding related mouse 22-kD proteins consisting of 211 and 230 amino acids, respectively. Hydrophilicity analysis suggested that both bore four transmembrane domains, although they did not show any sequence similarity to occludin. Immunofluorescence and immunoelectron microscopy revealed that both proteins tagged with FLAG or GFP were targeted to and incorporated into the TJ strand itself. We designated them as “claudin-1” and “claudin-2”, respectively. Although the precise structure/function relationship of the claudins to TJ still remains elusive, these findings indicated that multiple integral membrane proteins with four putative transmembrane domains, occludin and claudins, constitute TJ strands.
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            Claudin-based tight junctions are crucial for the mammalian epidermal barrier

            The tight junction (TJ) and its adhesion molecules, claudins, are responsible for the barrier function of simple epithelia, but TJs have not been thought to play an important role in the barrier function of mammalian stratified epithelia, including the epidermis. Here we generated claudin-1–deficient mice and found that the animals died within 1 d of birth with wrinkled skin. Dehydration assay and transepidermal water loss measurements revealed that in these mice the epidermal barrier was severely affected, although the layered organization of keratinocytes appeared to be normal. These unexpected findings prompted us to reexamine TJs in the epidermis of wild-type mice. Close inspection by immunofluorescence microscopy with an antioccludin monoclonal antibody, a TJ-specific marker, identified continuous TJs in the stratum granulosum, where claudin-1 and -4 were concentrated. The occurrence of TJs was also confirmed by ultrathin section EM. In claudin-1–deficient mice, claudin-1 appeared to have simply been removed from these TJs, leaving occludin-positive (and also claudin-4–positive) TJs. Interestingly, in the wild-type epidermis these occludin-positive TJs efficiently prevented the diffusion of subcutaneously injected tracer (∼600 D) toward the skin surface, whereas in the claudin-1–deficient epidermis the tracer appeared to pass through these TJs. These findings provide the first evidence that continuous claudin-based TJs occur in the epidermis and that these TJs are crucial for the barrier function of the mammalian skin.
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              A Single Gene Product, Claudin-1 or -2, Reconstitutes Tight Junction Strands and Recruits Occludin in Fibroblasts

              Three integral membrane proteins, clau- din-1, -2, and occludin, are known to be components of tight junction (TJ) strands. To examine their ability to form TJ strands, their cDNAs were introduced into mouse L fibroblasts lacking TJs. Immunofluorescence microscopy revealed that both FLAG-tagged claudin-1 and -2 were highly concentrated at cell contact sites as planes through a homophilic interaction. In freeze-fracture replicas of these contact sites, well-developed networks of strands were identified that were similar to TJ strand networks in situ and were specifically labeled with anti-FLAG mAb. In glutaraldehyde-fixed samples, claudin-1–induced strands were largely associated with the protoplasmic (P) face as mostly continuous structures, whereas claudin-2–induced strands were discontinuous at the P face with complementary grooves at the extracellular (E) face which were occupied by chains of particles. Although occludin was also concentrated at cell contact sites as dots through its homophilic interaction, freeze-fracture replicas identified only a small number of short strands that were labeled with anti-occludin mAb. However, when occludin was cotransfected with claudin-1, it was concentrated at cell contact sites as planes to be incorporated into well- developed claudin-1–based strands. These findings suggested that claudin-1 and -2 are mainly responsible for TJ strand formation, and that occludin is an accessory protein in some function of TJ strands.
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                Author and article information

                Contributors
                heidi.wilson@ucdenver.edu
                michael.rudolph@ucdenver.edu
                p.ramanathan@uni.sydney.edu.au
                valeribu@yahoo.com
                patricia.webb@ucdenver.edu
                Benjamin.bitler@ucdenver.edu
                torsten.stein@glasgow.ac.uk
                kkobaya@anim.agr.hokudai.ac.jp
                303-521-1645 , peggy.neville@ucdenver.edu
                Journal
                J Mammary Gland Biol Neoplasia
                J Mammary Gland Biol Neoplasia
                Journal of Mammary Gland Biology and Neoplasia
                Springer US (New York )
                1083-3021
                1573-7039
                28 April 2017
                28 April 2017
                2017
                : 22
                : 2
                : 141-157
                Affiliations
                [1 ]ISNI 0000 0001 0703 675X, GRID grid.430503.1, Department of Obstetrics and Gynecology, , University of Colorado Denver, ; Aurora, CO 80045 USA
                [2 ]ISNI 0000 0001 0703 675X, GRID grid.430503.1, Division of Endocrinology, Metabolism & Diabetes, , University of Colorado Denver, ; Aurora, CO 80045 USA
                [3 ]ISNI 0000 0001 1547 9964, GRID grid.176731.5, Department of Pathology, , University of Texas Medical Branch at Galveston, ; Galveston, TX 77555 USA
                [4 ]ISNI 0000 0001 0703 675X, GRID grid.430503.1, Department of Physiology and Biophysics, Anschutz Medical Center, , University of Colorado Denver, ; Aurora, CO 80045 USA
                [5 ]ISNI 0000 0001 2193 314X, GRID grid.8756.c, College of Medical, Veterinary and Life Sciences, , University of Glasgow, ; Glasgow, UK
                [6 ]ISNI 0000 0001 2173 7691, GRID grid.39158.36, Research Faculty of Agriculture, , Hokkaido University, ; Sapporo, 060-8589 Japan
                [7 ]6561 Glencoe St., Centennial, CO 80121 USA
                Article
                9379
                10.1007/s10911-017-9379-6
                5488167
                28455726
                327d5a9a-ecb2-4272-96b7-04eec5d53560
                © The Author(s) 2017

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 20 November 2016
                : 17 April 2017
                Categories
                Article
                Custom metadata
                © Springer Science+Business Media, LLC 2017

                Oncology & Radiotherapy
                mammary gland,claudin-1,claudin-3,claudin-4,claudin-7,claudin-8,extra-junctional claudin,involution,infection

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