Surfactant protein A








































surfactant, pulmonary-associated protein A1
Identifiers
Symbol SFTPA1
Alt. symbols SFTP1
Entrez 6435
HUGO 10798
OMIM 178630
RefSeq NM_005411
UniProt Q8IWL2
Other data
Locus
Chr. 10 q22.3

































surfactant, pulmonary-associated protein A2B
Identifiers
Symbol SFTPA2B
Entrez 6436
HUGO 10799
OMIM 178642
RefSeq NM_006926
UniProt Q8IWL1
Other data
Locus
Chr. 10 q22.3

Surfactant protein A is an innate immune system collectin. It is water-soluble and has collagen-like domains similar to SP-D. It is part of the innate immune system and is used to opsonize bacterial cells in the alveoli marking them for phagocytosis by alveolar macrophages. SP-A may also play a role in negative feedback limiting the secretion of pulmonary surfactant. SP-A is not required for pulmonary surfactant to function but does confer immune effects to the organism.[1]




Contents






  • 1 During Parturition


  • 2 Immune Functions


  • 3 Location


  • 4 See also


  • 5 External links


  • 6 References





During Parturition


The role of Surfactant protein A (or SP-A) in childbirth is indicated in studies with mice.[2] Mice which gestate for 19 days typically show signs of SP-A in amniotic fluid at around 16 days. If SP-A is injected into the uterus at 15 days, mice typically deliver early. Inversely, an SP-A inhibitor injection causes notable delays in birth.


The presence of Surfactant Protein A seemed to trigger an inflammatory response in the uterus of the mice, but later studies found an anti-inflammatory response in humans.[3] In fact, the level of SP-A in a human uterus typically decreases during labor.



Immune Functions


Research on SP-A has been done mainly in rodents including mice and rats. This research has shown that mice deficient in SP-A are more susceptible to infections from group B Streptoccoal organisms,[4] Pseudomonas aeruginosa,[5] and likely other organisms. The immune functions of SP-A are time, temperature, and concentration dependant.[6]



Location


SP-A is found in the pulmonary surfactant in lungs. SP-A and SP-D are also present in extrapulmonary tissues.[7]



See also



  • pulmonary surfactant

  • SFTPA1

  • SFTPA2



External links



  • Surfactant+Protein+A at the US National Library of Medicine Medical Subject Headings (MeSH)


References





  1. ^ Boron W, Boulpaep E (2012). Medical Physiology (2nd ed.). Philadelphia: Elsevier..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}


  2. ^ Condon JC, Jeyasuria P, Faust JM, Mendelson CR (April 2004). "Surfactant protein secreted by the maturing mouse fetal lung acts as a hormone that signals the initiation of parturition". Proceedings of the National Academy of Sciences of the United States of America. 101 (14): 4978–83. doi:10.1073/pnas.0401124101. JSTOR 3371804. PMC 387359. PMID 15044702.


  3. ^ Lee DC, Romero R, Kim CJ, Chaiworapongsa T, Tarca AL, Lee J, Suh YL, Mazaki-Tovi S, Vaisbuch E, Mittal P, Draghici S, Erez O, Kusanovic JP, Hassan SS, Kim JS (June 2010). "Surfactant protein-A as an anti-inflammatory component in the amnion: implications for human pregnancy". Journal of Immunology. 184 (11): 6479–91. doi:10.4049/jimmunol.0903867. PMC 3103775. PMID 20439915.


  4. ^ LeVine AM, Bruno MD, Huelsman KM, Ross GF, Whitsett JA, Korfhagen TR (May 1997). "Surfactant protein A-deficient mice are susceptible to group B streptococcal infection". Journal of Immunology. 158 (9): 4336–40. PMID 9126996.


  5. ^ LeVine AM, Kurak KE, Bruno MD, Stark JM, Whitsett JA, Korfhagen TR (October 1998). "Surfactant protein-A-deficient mice are susceptible to Pseudomonas aeruginosa infection". American Journal of Respiratory Cell and Molecular Biology. 19 (4): 700–8. doi:10.1165/ajrcmb.19.4.3254. PMID 9761768.


  6. ^ van Iwaarden F, Welmers B, Verhoef J, Haagsman HP, van Golde LM (January 1990). "Pulmonary surfactant protein A enhances the host-defense mechanism of rat alveolar macrophages". American Journal of Respiratory Cell and Molecular Biology. 2 (1): 91–8. doi:10.1165/ajrcmb/2.1.91. PMID 2306370.


  7. ^ Haagsman HP, Diemel RV (May 2001). "Surfactant-associated proteins: functions and structural variation". Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology. 129 (1): 91–108. PMID 11369536.









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