LYVE1

Last updated
LYVE1
Identifiers
Aliases LYVE1 , CRSBP-1, HAR, LYVE-1, XLKD1, lymphatic vessel endothelial hyaluronan receptor 1
External IDs OMIM: 605702 MGI: 2136348 HomoloGene: 4868 GeneCards: LYVE1
Gene location (Human)
Ideogram human chromosome 11.svg
Chr. Chromosome 11 (human) [1]
Human chromosome 11 ideogram.svg
HSR 1996 II 3.5e.svg
Red rectangle 2x18.png
Band 11p15.4Start10,556,966 bp [1]
End10,611,689 bp [1]
RNA expression pattern
PBB GE XLKD1 219059 s at fs.png

PBB GE XLKD1 220037 s at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_006691

NM_053247

RefSeq (protein)

NP_006682

NP_444477

Location (UCSC) Chr 11: 10.56 – 10.61 Mb Chr 7: 110.85 – 110.86 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Lymphatic vessel endothelial hyaluronan receptor 1 (LYVE1), also known as extracellular link domain containing 1 (XLKD1) is a Link domain-containing hyaladherin, a protein capable of binding to hyaluronic acid (HA), homologous to CD44, the main HA receptor. [5] In humans it is encoded by the LYVE1 gene. [6]

LYVE1 is a type I integral membrane glycoprotein. It acts as a receptor and binds to both soluble and immobilized hyaluronan. This protein may function in lymphatic hyaluronan transport and have a role in tumor metastasis. [6] LYVE-1 is a cell surface receptor on lymphatic endothelial cells that can be used as a lymphatic endothelial cell marker, allowing for the isolation of these cells for experimental purposes. The physiological role for this receptor is still the subject of debate, but evolutionary conservation suggests an important role.

Expression of LYVE1 not restricted to lymph vessels but is also observed in normal liver blood sinusoids, [7] and embryonic blood vessels. [8]

LYVE1 expression is also observed in subset of macrophages. [9] [10] LYVE1 positive macrophages in the meninges of rats are both lymphatic, as well as, alymphatic. [11] In brain dura, the LYVE1+ macrophages were predominantly pleomorphic in morphology, while the cells in the spinal cord were pleomorphic in the cervical dura, while in the thoracal dura the cells were mainly round in morphology. The cells in brain dura were associated with collagen network in meninges, and some nonlymphatic LYVE1+ macrophages contained intracellular collagen. The exact function of these cells is yet unknown.

Related Research Articles

Capillary Smallest type of blood vessel

A capillary is a small blood vessel from 5 to 10 micrometres (μm) in diameter, and having a wall one endothelial cell thick. They are the smallest blood vessels in the body: they convey blood between the arterioles and venules. These microvessels are the site of exchange of many substances with the interstitial fluid surrounding them. Substances which exit include water, oxygen, and glucose; substances which enter include water, carbon dioxide, uric acid, lactic acid, urea and creatinine. Lymph capillaries connect with larger lymph vessels to drain lymphatic fluid collected in the microcirculation.

Lymphatic system Organ system in vertebrates

The lymphatic system, or lymphoid system, is an organ system in vertebrates that is part of the circulatory system and the immune system. It is made up of a large network of lymph, lymphatic vessels, lymph nodes, lymphatic or lymphoid organs, and lymphoid tissues. The vessels carry a clear fluid called lymph towards the heart.

Endothelium Cells that line the Inner surface of blood vessels

Endothelium is a single layer of squamous endothelial cells that line the interior surface of blood vessels, and lymphatic vessels. The endothelium forms an interface between circulating blood or lymph in the lumen and the rest of the vessel wall. Endothelial cells form the barrier between vessels and tissue and control the flow of substances and fluid into and out of a tissue.

Kupffer cell

Kupffer cells, also known as stellate macrophages and Kupffer–Browicz cells, are specialized cells localized in liver within the lumen of the liver sinusoids and are adhesive to their endothelial cells which make up the blood vessel walls. Kupffer cells contain the largest amount of tissue-resident macrophages in the body. Gut bacteria, bacterial endotoxins, and microbial debris transported to the liver from the gastrointestinal tract via the portal vein will first come in contact with Kupffer cells, the first immune cells in the liver. It is because of this that any change to Kupffer cell functions can be connected to various liver diseases such as alcoholic liver disease, viral hepatitis, intrahepatic cholestasis, steatohepatitis, activation or rejection of the liver during liver transplantation and liver fibrosis. They form part of the mononuclear phagocyte system.

CD34 Cluster of differentiation protocol that identifies cell surface antigens.

CD34 is a transmembrane phosphoglycoprotein protein encoded by the CD34 gene in humans, mice, rats and other species.

CCL19

Chemokine ligand 19 (CCL19) is a protein that in humans is encoded by the CCL19 gene.

C-C chemokine receptor type 6

Chemokine receptor 6 also known as CCR6 is a CC chemokine receptor protein which in humans is encoded by the CCR6 gene. CCR6 has also recently been designated CD196. The gene is located on the long arm of Chromosome 6 (6q27) on the Watson (plus) strand. It is 139,737 bases long and encodes a protein of 374 amino acids.

Vascular endothelial growth factor C

Vascular endothelial growth factor C (VEGF-C) is a protein that is a member of the platelet-derived growth factor / vascular endothelial growth factor (PDGF/VEGF) family. It is encoded in humans by the VEGFC gene, which is located on chromosome 4q34.

C-fos-induced growth factor

C-fos-induced growth factor (FIGF) is a vascular endothelial growth factor that in humans is encoded by the FIGF gene.

PROX1

Prospero homeobox protein 1 is a protein that in humans is encoded by the PROX1 gene.

HAS2

Hyaluronan synthase 2 is an enzyme that in humans is encoded by the HAS2 gene.

HAS1

Hyaluronan synthase 1 is an enzyme that in humans is encoded by the HAS1 gene.

STAB1

Stabilin-1 is a protein that in humans is encoded by the STAB1 gene.

HAS3

Hyaluronan synthase 3 is an enzyme that in humans is encoded by the HAS3 gene.

STAB2

Stabilin-2 is a protein that in humans is encoded by the STAB2 gene.

The lymphatic endothelium is a specialised form of epithelium, distinct from but similar to vascular endothelium. A lymph capillary endothelial cell is distinct from other endothelial cells in that collagen fibers are directly attached to its plasma membrane.

Lymph sacs are a part of the development of the lymphatic system, known as lymphangiogenesis. The lymph sacs are precursors of the lymph vessels. These sacs develop through the processes of vasculogenesis and angiogenesis. However, there is evidence of both of these processes in different organisms. In mice, it is thought that the lymphatic components form through an angiogenic process. But, there is evidence from bird embryos that gives rise to the idea that lymphatic vessels arise in the embryos through a vasculogenesis-like process from the lymphangioblastic endothelial precursor cells.

Lymph node stromal cells are essential to the structure and function of the lymph node whose functions include: creating an internal tissue scaffold for the support of hematopoietic cells; the release of small molecule chemical messengers that facilitate interactions between hematopoietic cells; the facilitation of the migration of hematopoietic cells; the presentation of antigens to immune cells at the initiation of the adaptive immune system; and the homeostasis of lymphocyte numbers. Stromal cells originate from multipotent mesenchymal stem cells.

Meningeal lymphatic vessels

The meningeal lymphatic vessels are a network of conventional lymphatic vessels located parallel to the dural venous sinuses and middle meningeal arteries of the mammalian central nervous system (CNS). As a part of the lymphatic system, the meningeal lymphatics are responsible for draining immune cells, small molecules, and excess fluid from the CNS into the deep cervical lymph nodes. Cerebrospinal fluid, and interstitial fluid are exchanged, and drained by the meningeal lymphatic vessels.

Liver sinusoidal endothelial cells (LSECs) form the lining of the smallest blood vessels in the liver, also called the hepatic sinusoids. LSECs are highly specialized endothelial cells with characteristic morphology and function. They constitute an important part of the reticuloendothelial system (RES).

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000133800 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000030787 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Banerji S, Ni J, Wang SX, Clasper S, Su J, Tammi R, et al. (February 1999). "LYVE-1, a new homologue of the CD44 glycoprotein, is a lymph-specific receptor for hyaluronan". The Journal of Cell Biology. 144 (4): 789–801. doi:10.1083/jcb.144.4.789. PMC   2132933 . PMID   10037799.
  6. 1 2 "LYVE1 lymphatic vessel endothelial hyaluronan receptor 1 [ Homo sapiens (human) ]".
  7. Mouta Carreira C, Nasser SM, di Tomaso E, Padera TP, Boucher Y, Tomarev SI, Jain RK (November 2001). "LYVE-1 is not restricted to the lymph vessels: expression in normal liver blood sinusoids and down-regulation in human liver cancer and cirrhosis". Cancer Research. 61 (22): 8079–84. PMID   11719431.
  8. Gordon EJ, Gale NW, Harvey NL (July 2008). "Expression of the hyaluronan receptor LYVE-1 is not restricted to the lymphatic vasculature; LYVE-1 is also expressed on embryonic blood vessels". Developmental Dynamics. 237 (7): 1901–9. doi: 10.1002/dvdy.21605 . PMID   18570254. S2CID   21324950.
  9. Lee HW, Qin YX, Kim YM, Park EY, Hwang JS, Huo GH, et al. (February 2011). "Expression of lymphatic endothelium-specific hyaluronan receptor LYVE-1 in the developing mouse kidney". Cell and Tissue Research. 343 (2): 429–44. doi:10.1007/s00441-010-1098-x. PMID   21181199. S2CID   1904976.
  10. Maruyama K, Asai J, Ii M, Thorne T, Losordo DW, D'Amore PA (April 2007). "Decreased macrophage number and activation lead to reduced lymphatic vessel formation and contribute to impaired diabetic wound healing". The American Journal of Pathology. 170 (4): 1178–91. doi:10.2353/ajpath.2007.060018. PMC   1829452 . PMID   17392158.
  11. Brezovakova V, Jadhav S (January 2020). "Identification of Lyve-1 positive macrophages as resident cells in meninges of rats". The Journal of Comparative Neurology. 528 (12): 2021–2032. doi:10.1002/cne.24870. PMID   32003471. S2CID   210984721.

Further reading