Jump to content

Basement membrane

From Wikipedia, the free encyclopedia
Basement membrane
The epithelium and endobasement membrane in relation to epithelium and endothelium. Also seen are other extracellular matrix components
Image showing the basement membrane of the lining of the mouth, which separates the lining (epithelium) from a loose layer of connective tissue (the lamina propria)
Latinmembrana basalis
Anatomical terms of microanatomy

The basement membrane, also known as base membrane, is a thin, pliable sheet-like type of extracellular matrix that provides cell and tissue support and acts as a platform for complex signalling.[1][2] The basement membrane sits between epithelial tissues including mesothelium and endothelium, and the underlying connective tissue.[3][4]


Normal histology of the breast, with basement membrane annotated near center-right.
Prostate gland microanatomy, with basement membrane annotated at bottom.

As seen with the electron microscope, the basement membrane is composed of two layers, the basal lamina and the reticular lamina.[4] The underlying connective tissue attaches to the basal lamina with collagen VII anchoring fibrils and fibrillin microfibrils.[5]

The basal lamina layer can further be subdivided into two layers based on their visual appearance in electron microscopy. The lighter-colored layer closer to the epithelium is called the lamina lucida, while the denser-colored layer closer to the connective tissue is called the lamina densa. The electron-dense lamina densa layer is about 30–70 nanometers thick and consists of an underlying network of reticular collagen IV fibrils which average 30 nanometers in diameter and 0.1–2 micrometers in thickness and are coated with the heparan sulfate-rich proteoglycan perlecan.[6] In addition to collagen, this supportive matrix contains intrinsic macromolecular components. The lamina lucida layer is made up of laminin, integrins, entactins, and dystroglycans. Integrins are a key component of hemidesmosomes which serve to anchor the epithelium to the underlying basement membrane.

To represent the above in a visually organised manner, the basement membrane is organized as follows:



The primary function of the basement membrane is to anchor down the epithelium to its loose connective tissue (the dermis or lamina propria) underneath. This is achieved by cell-matrix adhesions through substrate adhesion molecules (SAMs).

The basement membrane acts as a mechanical barrier, preventing malignant cells from invading the deeper tissues.[7] Early stages of malignancy that are thus limited to the epithelial layer by the basement membrane are called carcinoma in situ.

The basement membrane is also essential for angiogenesis (development of new blood vessels). Basement membrane proteins have been found to accelerate differentiation of endothelial cells.[8]

The most notable examples of basement membranes is the glomerular basement membrane of the kidney, by the fusion of the basal lamina from the endothelium of glomerular capillaries and the podocyte basal lamina,[9] and between lung alveoli and pulmonary capillaries, by the fusion of the basal lamina of the lung alveoli and of the basal lamina of the lung capillaries, which is where oxygen and CO2 diffusion occurs (gas exchange).

As of 2017, other roles for basement membrane include blood filtration and muscle homeostasis.[1] Fractones may be a type of basement membrane, serving as a niche for stem cells.[10][11]

Clinical significance


Some diseases result from a poorly functioning basement membrane. The cause can be genetic defects, injuries by the body's own immune system, or other mechanisms.[12] Diseases involving basement membranes at multiple locations include:

In histopathology, thickened basement membranes are found in several inflammatory diseases, such as lichen sclerosus, systemic lupus erythematosus or dermatomyositis in the skin, or collagenous colitis in the colon.[15]

Evolutionary origin


These are only found within diploblastic and homoscleromorphic sponge animals. The homoscleromorph were found to be sister to diploblasts in some studies, making the membrane originate once in the history of life. But more recent studies have disregarded diploblast-homoscleromorph group, so other sponges may have lost it (most probable) or the origin in the two groups may be separate.

See also



  1. ^ a b Pozzi A, Yurchenco PD, Iozzo RV (January 2017). "The nature and biology of basement membranes". Matrix Biology. 57–58: 1–11. doi:10.1016/j.matbio.2016.12.009. PMC 5387862. PMID 28040522.
  2. ^ Sekiguchi R, Yamada KM (2018). "Basement Membranes in Development and Disease". Current Topics in Developmental Biology. 130: 143–191. doi:10.1016/bs.ctdb.2018.02.005. ISBN 9780128098028. PMC 6701859. PMID 29853176.
  3. ^ Kierszenbaum A, Tres L (2012). Histology and Cell Biology, An Introduction to Pathology (3rd ed.). Elsevier. ISBN 978-0-323-07842-9.
  4. ^ a b Tortora G, Derrickson B (2012). Principles of anatomy & physiology (13th ed.). Hoboken, NJ: Wiley. pp. 117–118. ISBN 9780470646083.
  5. ^ Paulsson M (1992). "Basement membrane proteins: structure, assembly, and cellular interactions". Critical Reviews in Biochemistry and Molecular Biology. 27 (1–2): 93–127. doi:10.3109/10409239209082560. PMID 1309319. Archived from the original on 2007-10-13.
  6. ^ Noonan DM, Fulle A, Valente P, Cai S, Horigan E, Sasaki M, et al. (December 1991). "The complete sequence of perlecan, a basement membrane heparan sulfate proteoglycan, reveals extensive similarity with laminin A chain, low density lipoprotein-receptor, and the neural cell adhesion molecule". The Journal of Biological Chemistry. 266 (34): 22939–22947. doi:10.1016/S0021-9258(18)54445-8. PMID 1744087.
  7. ^ Liotta LA, Tryggvason K, Garbisa S, Hart I, Foltz CM, Shafie S (March 1980). "Metastatic potential correlates with enzymatic degradation of basement membrane collagen". Nature. 284 (5751): 67–68. Bibcode:1980Natur.284...67L. doi:10.1038/284067a0. PMID 6243750. S2CID 4356057.
  8. ^ Kubota Y, Kleinman HK, Martin GR, Lawley TJ (October 1988). "Role of laminin and basement membrane in the morphological differentiation of human endothelial cells into capillary-like structures". The Journal of Cell Biology. 107 (4): 1589–1598. doi:10.1083/jcb.107.4.1589. PMC 2115245. PMID 3049626.
  9. ^ "Sect. 7, Ch. 4: Basement Membrane". Renal Physiology Glomerular Filtration Rate and Renal Blood Flow. Medical College of Georgia, Robert B. Greenblatt, M.D. Library. 1 April 2008. Archived from the original on 1 April 2008. Retrieved 7 May 2018.{{cite book}}: CS1 maint: bot: original URL status unknown (link)
  10. ^ Mercier F, Kitasako JT, Hatton GI (September 2002). "Anatomy of the brain neurogenic zones revisited: fractones and the fibroblast/macrophage network". The Journal of Comparative Neurology. 451 (2): 170–188. doi:10.1002/cne.10342. PMID 12209835. S2CID 19919800.
  11. ^ Sato Y, Kiyozumi D, Futaki S, Nakano I, Shimono C, Kaneko N, et al. (January 2019). Yamashita Y (ed.). "Ventricular-subventricular zone fractones are speckled basement membranes that function as a neural stem cell niche". Molecular Biology of the Cell. 30 (1): 56–68. doi:10.1091/mbc.E18-05-0286. PMC 6337917. PMID 30379609.
  12. ^ Henig RM (February 22, 2009). "What's Wrong With Summer Stiers?". New York Times. Archived from the original on November 9, 2016.
  13. ^ Janeway CA (2001). Immunobiology (5th ed.). Garland. ISBN 978-0-8153-3642-6.
  14. ^ Bardhan A, Bruckner-Tuderman L, Chapple IL, Fine JD, Harper N, Has C, et al. (September 2020). "Epidermolysis bullosa". Nature Reviews. Disease Primers. 6 (1): 78. doi:10.1038/s41572-020-0210-0. PMID 32973163. S2CID 221861310.
  15. ^ LeBoit PE (October 2000). "A thickened basement membrane is a clue to...lichen sclerosus!". The American Journal of Dermatopathology. 22 (5): 457–458. doi:10.1097/00000372-200010000-00014. PMID 11048985.

Further reading