For other uses, see Capillary (disambiguation).
Capillary vessel

Transmission electron microscope image of a capillary with a red blood cell within the pancreas. The capillary lining consists of long, thin endothelial cells, connected by tight junctions.

A simplified illustration of a capillary network (lacking precapillary sphincters, which are not present in all capillaries[1]).
Latin vas capillare[2]
Code TH H3.
TA A12.0.00.025
FMA 63195

Anatomical terminology

Capillaries (/ˈkæplɛriz/ in US; /kəˈpɪləriz/ in UK) are the smallest of a body's blood vessels (and lymph vessels) that make up the microcirculation. Their endothelial linings are only one cell layer thick. These microvessels, measuring around 5 to 10 micrometres (µm) in diameter, connect arterioles and venules, and they help to enable the exchange of water, oxygen, carbon dioxide, and many other nutrients and waste substances between the blood and the tissues[3] surrounding them. Lymph capillaries connect with larger lymph vessels to drain lymph collected in the microcirculation.

During early embryonic development[4] new capillaries are formed through vasculogenesis, the process of blood vessel formation that occurs through a de novo production of endothelial cells which then form vascular tubes.[5] The term angiogenesis denotes the formation of new capillaries from pre-existing blood vessels and already present endothelium which divides.[6]


Diagram of a capillary

Blood flows from the heart through arteries, which branch and narrow into arterioles, and then branch further into capillaries where nutrients and wastes are exchanged. The capillaries then join and widen to become venules, which in turn widen and converge to become veins, which then return blood back to the heart through the great veins.

Capillaries do not function on their own, but instead in a capillary bed, an interweaving network of capillaries supplying organs and tissues. The more metabolically active a cell or environment is, the more capillaries are required to supply nutrients and carry away waste products. Capillary beds can consist of two types of vessels: true capillaries, which branch from arterioles and provide exchange between cells and the blood, and short vessels that directly connect the arterioles and venules at opposite ends of the beds, metarterioles, only found in the mesenteric circulation.

Metarterioles are found primarily (or exclusively) in the mesenteric microcirculation[1] and were erroneously thought to be present in most or all capillary beds.[1] The physiological mechanisms underlying precapillary resistance is no longer considered to be a result of precapillary sphincters outside of the mesentery organ.[1]

Lymphatic capillaries are slightly larger in diameter than blood capillaries, and have closed ends (unlike the blood capillaries open at one end to the arterioles and open at the other end to the venules). This structure permits interstitial fluid to flow into them but not out. Lymph capillaries have a greater internal oncotic pressure than blood capillaries, due to the greater concentration of plasma proteins in the lymph.[7]


There are three main types of blood capillaries:

Depiction of the major types of capillaries, showing fenestrations as well as intercellular gaps.


Continuous capillaries are continuous in the sense that the endothelial cells provide an uninterrupted lining, and they only allow smaller molecules, such as water and ions to pass through their intercellular clefts. However lipid-soluble molecules can passively diffuse through the endothelial cell membranes along concentration gradients. Tight junctions can be further divided into two subtypes:

  1. Those with numerous transport vesicles, which are found primarily in skeletal muscles, fingers, gonads, and skin.
  2. Those with few vesicles, which are primarily found in the central nervous system. These capillaries are a constituent of the blood–brain barrier.


Fenestrated capillaries (derived from fenestra, Latin for "window") have pores in the endothelial cells (60-80 nm in diameter) that are spanned by a diaphragm of radially oriented fibrils and allow small molecules and limited amounts of protein to diffuse.[8][9] In the renal glomerulus there are cells with no diaphragms, called podocyte foot processes or pedicels, which have slit pores with a function analogous to the diaphragm of the capillaries. Both of these types of blood vessels have continuous basal laminae and are primarily located in the endocrine glands, intestines, pancreas, and the glomeruli of the kidney.


Sinusoidal capillaries are a special type of open-pore capillary also known as a discontinuous capillary, that have larger openings (30-40 µm in diameter) in the endothelium. These types of blood vessels allow red and white blood cells (7.5 µm - 25 µm diameter) and various serum proteins to pass, aided by a discontinuous basal lamina. These capillaries lack pinocytotic vesicles, and therefore utilize gaps present in cell junctions to permit transfer between endothelial cells, and hence across the membrane. Sinusoid blood vessels are primarily located in the bone marrow, lymph nodes, and adrenal glands. Some sinusoids are distinctive in that they do not have the tight junctions between cells. They are called discontinuous sinusoidal capillaries, and are present in the liver and spleen, where greater movement of cells and materials is necessary. A capillary wall is only 1 cell thick and is simple squamous epithelium.


Simplified image showing blood-flow through the body, passing through capillary networks in its path.

The capillary wall performs an important function by allowing nutrients and waste substances to pass across it. Molecules larger than 3 nm such as albumin and other large proteins pass through transcellular transport carried inside vesicles, a process which requires them to go through the cells that form the wall. Molecules smaller than 3 nm such as water, ions and gases cross the capillary wall through the space between cells in a process known as paracellular transport.[10] These transport mechanisms allow bidirectional exchange of substances depending on osmotic gradients and can be further quantified by the Starling equation.[11] Capillaries that form part of the blood–brain barrier however only allow for transcellular transport as tight junctions between endothelial cells seal the paracellular space.[12]

Capillary beds may control their blood flow via autoregulation. This allows an organ to maintain constant flow despite a change in central blood pressure. This is achieved by myogenic response, and in the kidney by tubuloglomerular feedback. When blood pressure increases, arterioles are stretched and subsequently constrict (a phenomenon known as the Bayliss effect) to counteract the increased tendency for high pressure to increase blood flow.

In the lungs special mechanisms have been adapted to meet the needs of increased necessity of blood flow during exercise. When the heart rate increases and more blood must flow through the lungs, capillaries are recruited and are also distended to make room for increased blood flow. This allows blood flow to increase while resistance decreases.

Capillary permeability can be increased by the release of certain cytokines, anaphylatoxins, or other mediators (such as leukotrienes, prostaglandins, histamine, bradykinin, etc.) highly influenced by the immune system.

Depiction of the filtration and reabsorption present in capillaries.

The Starling equation defines the forces across a semipermeable membrane and allows calculation of the net flux:


By convention, outward force is defined as positive, and inward force is defined as negative. The solution to the equation is known as the net filtration or net fluid movement (Jv). If positive, fluid will tend to leave the capillary (filtration). If negative, fluid will tend to enter the capillary (absorption). This equation has a number of important physiologic implications, especially when pathologic processes grossly alter one or more of the variables.


According to Starling's equation, the movement of fluid depends on six variables:

  1. Capillary hydrostatic pressure ( Pc )
  2. Interstitial hydrostatic pressure ( Pi )
  3. Capillary oncotic pressure ( πz )
  4. Interstitial oncotic pressure ( πi )
  5. Filtration coefficient ( Kf )
  6. Reflection coefficient ( σ )

Clinical significance

Disorders of capillary formation as a developmental defect or acquired disorder are a feature in many common and serious disorders. Within a wide range of cellular factors and cytokines, issues with normal genetic expression and bioactivity of the vascular growth and permeability factor vascular endothelial growth factor (VEGF) appear to play a major role in many of the disorders. Cellular factors include reduced number and function of bone-marrow derived endothelial progenitor cells.[13] and reduced ability of those cells to form blood vessels.[14]


Major diseases where altering capillary formation could be helpful include conditions where there is excessive or abnormal capillary formation such as cancer and disorders harming eyesight; and medical conditions in which there is reduced capillary formation either for familial or genetic reasons, or as an acquired problem.

Blood sampling

Capillary blood sampling can be used to test for, for example, blood glucose (such as in blood glucose monitoring), hemoglobin, pH and lactate (the two latter can be quantified in fetal scalp blood testing to check the acid base status of a fetus during childbirth).

Capillary blood sampling is generally performed by creating a small cut using a blood lancet, followed by sampling by capillary action on the cut with a test strip or small pipe.


Contrary to a popular misconception, William Harvey did not explicitly predict the existence of capillaries, but he clearly saw the need for some sort of connection between the arterial and venous systems. He wrote, "…the blood doth enter into every member through the arteries, and does return by the veins, and that the veins are the vessels and ways by which the blood is returned to the heart itself; and that the blood in the members and extremities does pass from the arteries into the veins (either mediately by an anastomosis, or immediately through the porosities of the flesh, or both ways) as before it did in the heart and thorax out of the veins, into the arteries…" [On the Motion of the Heart and Blood in Animals," Chapter XI, pp. 59–60 in 1653 edition.][18]

Marcello Malpighi was the first to observe directly and correctly describe capillaries, discovering them in a frog's lung in 1661.[19]

See also


  1. 1 2 3 4 Sakai et. al (2013). "Are the precapillary sphincters and metarterioles universal components of the microcirculation? An historical review". J Physiol Sci. 2013; 63: 319–331. 63 (5): 319–31. doi:10.1007/s12576-013-0274-7. PMC 3751330Freely accessible. PMID 23824465.
  2. "THH:3.09 The cardiovascular system". Retrieved June 3, 2014.
  3. Maton, Anthea; Jean Hopkins; Charles William McLaughlin; Susan Johnson; Maryanna Quon Warner; David LaHart; Jill D. Wright (1993). Human Biology and Health. Englewood Cliffs, New Jersey: Prentice Hall. ISBN 0-13-981176-1.
  5. John S. Penn (11 March 2008). Retinal and Choroidal Angiogenesis. Springer. pp. 119–. ISBN 978-1-4020-6779-2. Retrieved 26 June 2010.
  6. "Endoderm -- Developmental Biology -- NCBI Bookshelf". Retrieved 2010-04-07.
  7. Guyton, Arthur; Hall, John (2006). "Chapter 16: The Microcirculation and the Lymphatic System". In Gruliow, Rebecca. Textbook of Medical Physiology (Book) (11th ed.). Philadelphia, Pennsylvania: Elsevier Inc. pp. 187–188. ISBN 0-7216-0240-1
  8. Histology image:22401lba from Vaughan, Deborah (2002). A Learning System in Histology: CD-ROM and Guide. Oxford University Press. ISBN 978-0195151732.
  9. Pavelka, Margit; Jürgen Roth (2005). Functional Ultrastructure: An Atlas of Tissue Biology and Pathology. Springer. p. 232.
  10. Sukriti, S; Tauseef, M; Yazbeck, P; Mehta, D (2014). "Mechanisms regulating endothelial permeability.". Pulmonary circulation. 4 (4): 535–551. doi:10.1086/677356. PMC 4278616Freely accessible. PMID 25610592.
  11. Nagy, JA; Benjamin, L; Zeng, H; Dvorak, AM; Dvorak, HF (2008). "Vascular permeability, vascular hyperpermeability and angiogenesis.". Angiogenesis. 11 (2): 109–119. doi:10.1007/s10456-008-9099-z. PMC 2480489Freely accessible. PMID 18293091.
  12. Bauer, HC; Krizbai, IA; Bauer, H; Traweger, A (2014). ""You Shall Not Pass"-tight junctions of the blood brain barrier.". Frontiers in Neuroscience. 8. doi:10.3389/fnins.2014.00392. PMC 4253952Freely accessible. PMID 25520612.
  13. Gittenberger-De Groot, Adriana C.; Winter, Elizabeth M.; Poelmann, Robert E (2010). "Epicardium derived cells (EPDCs) in development, cardiac disease and repair of ischemia". Journal of Cellular and Molecular Medicine. 14 (5): 1056–60. doi:10.1111/j.1582-4934.2010.01077.x. PMID 20646126.
  14. 1 2 Lambiase, P. D.; Edwards, RJ; Anthopoulos, P; Rahman, S; Meng, YG; Bucknall, CA; Redwood, SR; Pearson, JD; Marber, MS (2004). "Circulating Humoral Factors and Endothelial Progenitor Cells in Patients with Differing Coronary Collateral Support". Circulation. 109 (24): 2986–92. doi:10.1161/01.CIR.0000130639.97284.EC. PMID 15184289.
  15. Noon, J P; Walker, B R; Webb, D J; Shore, A C; Holton, D W; Edwards, H V; Watt, G C (1997). "Impaired microvascular dilatation and capillary rarefaction in young adults with a predisposition to high blood pressure". Journal of Clinical Investigation. 99 (8): 1873–9. doi:10.1172/JCI119354. PMC 508011Freely accessible. PMID 9109431.
  16. Bird, Alan C. (2010). "Therapeutic targets in age-related macular disease". Journal of Clinical Investigation. 120 (9): 3033–41. doi:10.1172/JCI42437. PMC 2929720Freely accessible. PMID 20811159.
  17. Cao, Yihai (2009). "Tumor angiogenesis and molecular targets for therapy". Frontiers in Bioscience. 14 (14): 3962–73. doi:10.2741/3504. PMID 19273326.
  18. Harvey, William (1653). On the motion of the Heart and Blood in Animals. pp. 59–60.
  19. John Cliff, Walter (1976). Blood Vessels. CUP Archives. p. 14.
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