Cited by 44Connexins and lens biologyLymphatic System and DiseasesLymphatic Disorders and Treatments

Connexins in lymphatic vessel physiology and disease

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Meens, Merlijn J., Sabine, Amélie, Petrova, Tatiana V., Kwak, Brenda R.·2014·FEBS Letters

Abstract

Connexins are transmembrane proteins that form gap junction‐ and hemi‐channels. Once inserted into the membrane, hemi‐channels (connexons) allow for diffusion of ions and small molecules (<1 kDa) between the extracellular space and the cytosol. Gap junction channels allow diffusion of similar molecules between the cytoplasms of adjacent cells. The expression and function of connexins in blood vessels has been intensely studied in the last few decades. In contrast, only a few studies paid attention to lymphatic vessels; convincing in vivo data with respect to expression patterns of lymphatic connexins and their functional roles have only recently begun to emerge. Interestingly, mutations in connexin genes have been linked to diseases of lymphatic vasculature, most notably primary and secondary lymphedema. This review summarizes the available data regarding lymphatic connexins. More specifically it addresses (i) early studies aimed at presence of gap junction‐like structures in lymphatic vessels, (ii) more recent studies focusing on lymphatic connexins using genetically engineered mice, and (iii) results of clinical studies that have reported lymphedema‐linked mutations in connexin genes.

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Crossref · 10.1016/j.febslet.2014.01.011

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  • Conduction of LEC-dependent hyperpolarization to LMCs does not occur in collecting vessels, which do not express the connexin isoform Gja5/Cx40 mediating electrical continuity between endothelial cell and SM layers in arteries.

    “Conduction of LEC-dependent hyperpolarization to LMCs does not occur in collecting vessels, which do not express the connexin isoform (Gja5, Cx40) mediating electrical continuity between the endothelial cell and SM layers in arteries (70, 71).”

    From Transport and Immune Functions of the Lymphatic System. (2025) · cites this paper as [71]

    Section 6 reports that Cx40 could not be detected in lymphatic endothelium at any developmental stage, supporting the claim about its absence in collecting vessels. The paper does not establish that LEC-dependent hyperpolarization fails to reach lymphatic muscle cells, or that Cx40 mediates electrical continuity between endothelial and smooth-muscle layers in arteries. (LLM, conf=0.87)

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Authors
Meens, M. J., Sabine, A., Petrova, T. V., & Kwak, B. R.
Affiliations
  • University of Geneva (CH)
  • Centre Hospitalier Universitaire Vaudois (CH)
Corresponding author
Kwak, Brenda R.
Venue
FEBS Letters
Publisher
Wiley
Published
2014-01-20
Volume
588
Issue
8
Pages
1271-1277
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
OpenAlex
W2009283835
Cited by
44
References
2
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 3 · 2022: 3 · 2021: 4 · 2020: 4 · 2019: 2 · 2018: 7 · 2017: 3 · 2016: 2 · 2015: 8 · 2014: 4
FWCI
0.53
Type
journal article
Language
en
Open access
Locations
  • FEBS Letters (publishedVersion)
  • PubMed (publishedVersion)
  • Archive ouverte UNIGE (University of Geneva) (publishedVersion)
  • IRIS (submittedVersion)
  • SERVAL (Université de Lausanne) (submittedVersion)
  • Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
Funders
the Swiss National Science Foundation (310030_143343/1, PPP0033-114898, CRSII3_141811)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Connexins and lens biology
  • Health Sciences › Medicine › Oncology › Lymphatic System and Diseases
  • Health Sciences › Medicine › Surgery › Lymphatic Disorders and Treatments
Keywords
connexins, lymphatic vessels, gap junctions, hemichannels, lymphedema, primary lymphedema, secondary lymphedema, genetically modified mice
MeSH terms
Animals, Humans, Lymphedema, Mutation, Gap Junctions, Connexins, Lymphatic Vessels

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