Endothelium

This article is about the lining of blood and lymphatic vessels. For the endothelium of the cornea, see corneal endothelium.

Endothelium
Diagram showing the location of endothelial cells
Transmission electron micrograph of a microvessel showing endothelial cells, which encircle an erythrocyte (E), forming the innermost layer of the vessel, the tunica intima.
Details
System	Circulatory system
Location	Lining of the inner surface of blood vessels and lymphatic vessels
Identifiers
MeSH	D004727
TH	H2.00.02.0.02003
FMA	63916
Anatomical terms of microanatomy [edit on Wikidata]

Endothelium refers to cells that line the interior surface of blood vessels and lymphatic vessels,^[1] forming an interface between circulating blood or lymph in the lumen and the rest of the vessel wall. It is a thin layer of simple, or single-layered, squamous cells called endothelial cells. Endothelial cells in direct contact with blood are called vascular endothelial cells, whereas those in direct contact with lymph are known as lymphatic endothelial cells.

Vascular endothelial cells line the entire circulatory system, from the heart to the smallest capillaries. These cells have unique functions in vascular biology. These functions include fluid filtration, such as in the glomerulus of the kidney, blood vessel tone, hemostasis, neutrophil recruitment, and hormone trafficking. Endothelium of the interior surfaces of the heart chambers is called endocardium.

Contents

• 
  1 Structure
  
  
  
  • 
    1.1 Terminology
    
  
  
  
  


• 
  2 Function
  


• 
  3 Clinical significance
  


• 
  4 See also
  


• 
  5 References
  


• 
  6 External links
  

Structure

Endothelium is mesodermal in origin. Both blood and lymphatic capillaries are composed of a single layer of endothelial cells called a monolayer. In straight sections of a blood vessel, vascular endothelial cells typically align and elongate in the direction of fluid flow.^[2][3]

Terminology

The foundational model of anatomy makes a distinction between endothelial cells and epithelial cells on the basis of which tissues they develop from, and states that the presence of vimentin rather than keratin filaments separate these from epithelial cells.^[4] Many considered the endothelium a specialized epithelial tissue.^[5]

Function

Endothelium lines the inner wall of vessels, shown here.

Endothelial cells are involved in many aspects of vascular biology, including:

• Barrier function - the endothelium acts as a semi-selective barrier between the vessel lumen and surrounding tissue, controlling the passage of materials and the transit of white blood cells into and out of the bloodstream. Excessive or prolonged increases in permeability of the endothelial monolayer, as in cases of chronic inflammation, may lead to tissue edema/swelling.


• 
  Blood clotting (thrombosis & fibrinolysis). The endothelium normally provides a non-thrombogenic surface because it contains, for example, heparan sulfate which acts as a cofactor for activating antithrombin, a protease that inactivates several factors in the coagulation cascade.


• 
  Inflammation^[6]
  


• Formation of new blood vessels (angiogenesis)


• 
  Vasoconstriction and vasodilation, and hence the control of blood pressure
  


• Repair of damaged or diseased organs via an injection of blood vessel cells^[7]
  


• 
  Angiopoietin-2 works with VEGF to facilitate cell proliferation and migration of endothelial cells

Clinical significance

Main article: Endothelial dysfunction

Endothelial dysfunction, or the loss of proper endothelial function, is a hallmark for vascular diseases, and is often regarded as a key early event in the development of atherosclerosis. Impaired endothelial function, causing hypertension and thrombosis, is often seen in patients with coronary artery disease, diabetes mellitus, hypertension, hypercholesterolemia, as well as in smokers. Endothelial dysfunction has also been shown to be predictive of future adverse cardiovascular events, and is also present in inflammatory disease such as rheumatoid arthritis and systemic lupus erythematosus. One of the main mechanisms of endothelial dysfunction is the diminishing of nitric oxide, often due to high levels of asymmetric dimethylarginine, which interfere with the normal L-arginine-stimulated nitric oxide synthesis and so leads to hypertension. The most prevailing mechanism of endothelial dysfunction is an increase in reactive oxygen species, which can impair nitric oxide production and activity via several mechanisms.^[8] The signalling protein ERK5 is essential for maintaining normal endothelial cell function.^[9] A further consequence of damage to the endothelium is the release of pathological quantities of von Willebrand factor, which promote platelet aggregation and adhesion to the subendothelium, and thus the formation of potentially fatal thrombi.

See also

• Apelin


• Caveolae


• Cellular dewetting


• Endothelial activation


• Endothelial microparticle


• Endothelial progenitor cell


• 
  Endothelium-derived relaxing factor (EDRF)


• 
  Robert F. Furchgott (1998 Nobel prize for discovery of EDRF)


• Platelet activation


• Susac's syndrome


• Tunica intima


• VE-cadherin


• Weibel–Palade body


• Angiocrine growth factors

References

1. 
   ^ "Endothelium" at Dorland's Medical Dictionary
   
   


2. 
   ^ Eskin, S.G.; Ives, C.L.; McIntire, L.V.; Navarro, L.T. "Response of cultured endothelial cells to steady flow". Microvascular Research. 28 (1): 87–94. doi:10.1016/0026-2862(84)90031-1..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
   


3. 
   ^ Langille, B L; Adamson, S L (1981). "Relationship between blood flow direction and endothelial cell orientation at arterial branch sites in rabbits and mice". Circulation Research. 48: 481–488. doi:10.1161/01.RES.48.4.481.
   


4. 
   ^ "FMA". Archived from the original on 2013-10-02. Retrieved 2013-09-28.
   


5. 
   ^ Kovacic, Jason; Mercader, Nadia; Torres, Miguel; Boehm, Manfred; Fuster, Valentin (2012). "Cardiovascular Development to Disease Epithelial-to-Mesenchymal and Endothelial-to-Mesenchymal Transition: From Cardiovascular Development to Disease". Circulation. 125: 1795–1808. doi:10.1161/circulationaha.111.040352. PMC 3333843. Retrieved 8 November 2014.
   


6. 
   ^ Li X, Fang P, et al. (April 2016). "Mitochondrial Reactive Oxygen Species Mediate Lysophosphatidylcholine-Induced Endothelial Cell Activation". Arteriosclerosis, Thrombosis, and Vascular Biology. 36: 1090–100. doi:10.1161/ATVBAHA.115.306964. PMC 4882253. PMID 27127201.
   


7. 
   ^ "Blood vessel cells can repair, regenerate organs, scientists say". Retrieved 2018-11-13.
   


8. 
   ^ Deanfield J, Donald A, Ferri C, Giannattasio C, Halcox J, Halligan S, Lerman A, Mancia G, Oliver JJ, Pessina AC, Rizzoni D, Rossi GP, Salvetti A, Schiffrin EL, Taddei S, Webb DJ (January 2005). "Endothelial function and dysfunction. Part I: Methodological issues for assessment in the different vascular beds: a statement by the Working Group on Endothelin and Endothelial Factors of the European Society of Hypertension". J Hypertens. 23 (1): 7–17. doi:10.1097/00004872-200501000-00004. PMID 15643116.
   


9. 
   ^ Roberts OL, Holmes K, Müller J, Cross DA, Cross MJ (Dec 2009). "ERK5 and the regulation of endothelial cell function". Biochem Soc Trans. 37 (6): 1254–9. doi:10.1042/BST0371254. PMID 19909257.
   

External links

• 
  Anatomy photo: Circulatory/vessels/capillaries1/capillaries3 - Comparative Organology at University of California, Davis, "Capillaries, non-fenestrated (EM, Low)"


• 
  Histology image: 21402ooa – Histology Learning System at Boston University


• 
  Endothelium Journal of Endothelial Cell Research, Informa Healthcare
  


• Endothelium and inflammation


• 
  Platelet Activation, University of Washington
  

v t e Epithelial tissue
Cells	Squamous Cuboidal Columnar
Types	Simple squamous epithelium Endothelium Mesothelium Simple cuboidal epithelium Simple columnar epithelium Pseudostratified columnar epithelium Respiratory epithelium Stratified squamous epithelium Stratified cuboidal epithelium Stratified columnar epithelium Transitional epithelium Urothelium
Glands	Types Mechanism Merocrine Eccrine Apocrine Holocrine Sebaceous Meibomian Shape Tubular gland Alveolar gland Secretion Serous glands Mucous glands Components Myoepithelial cell Serous demilune Ducts: Interlobar Interlobular Intralobular Striated Intercalated Acinus/Lobe

v t e Arteries and veins
Vessels	Arteries Nutrient artery Arteriole Metarteriole Elastic artery Capillaries Types Continuous Fenestrated Sinusoidal Precapillary sphincter Precapillary resistance Veins Vena comitans Superficial vein Deep vein Emissary veins Venous plexus Venule Lymph Lymphatic vessel Lymph Lymph capillary
Circulatory system	Systemic Left heart → Aorta → Arteries → Arterioles → Capillaries → Venules → Veins → Vena cava → (Right heart) Pulmonary Right heart → Pulmonary arteries → Lungs → Pulmonary vein → Left heart
Microanatomy	Microvessel Microcirculation Tunica intima Endothelium Internal elastic lamina Tunica media Tunica externa Vasa vasorum Vasa nervorum Vascular nerves Rete mirabile Circulatory anastomosis

Authority control	TH: H2.00.02.0.02003

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