CD45: Diferenzas entre revisións

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O '''CD45''' ([[cluster de diferenciación|''cluster'' de diferenciación]]), chamado inicialmente '''antíxeno común leucocitario''', e chamado agora '''PTPRC''' (''Protein Tyrosine Phospatase, Receptor Typetype, C'', proteína tirosina fosfatase, tipo receptor, C) é un [[encima]] que se encontra na superficie de certas células[[leucocito]]s, que nos humanos está codificado no [[xene]] do [[cromosoma 1]].<ref name="pmid2169617">{{cite journal | author = Kaplan R, Morse B, Huebner K, ''et al'' | title = Cloning of three human tyrosine phosphatases reveals a multigene family of receptor-linked protein-tyrosine-phosphatases expressed in brain | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 87 | issue = 18 | pages = 7000–4 | year = 1990 | month = September | pmid = 2169617 | pmc = 54670 | doi = 10.1073/pnas.87.18.7000| url = http://www.pnas.org/cgi/pmidlookup?view=long&pmid=2169617 | issn = }}</ref> <ref name="entrez">{{cite web | title = Entrez Gene: PTPRC protein tyrosine phosphatase, receptor type, C| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5788| accessdate = }}</ref>
 
== Función ==
 
A proteína codificada por este xene é un membro da familia da [[proteína tirosina fosfatase]] (PTP). As PTPs son moléculas de [[sinalización celular]] que regulan diversos procesos celulares como o crecemento celular, diferenciación, [[ciclo celular|ciclo mitótico]], e a transformación oncoxénica. Estas PTP conteñen un dominio extracelular, un só segmento transmembrana e dous tándem de dominios catalíticos intracitoplasmáticos, polo que pertence ás PTP de tipo receptor. Este xene exprésase especificamente en células hematopoiéticas. Esta PTP é un regulador esencial da sinalización do receptor de antíxenos das células T e B ([[TCR]], [[BCR]]). Funciona por interacción directa con compoñentes dos complexos do receptor de antíxenos ou tamén activando varias [[quinase]]s da familia Src requiridas para a sinalización do receptor de antíxenos. Esta PTP tamén suprime as quinases JAK, e, deste modo, funciona como un regulador negativo da sinalización do receptor de citocinas. Informouse da existencia neste xene de catro variantes de [[transcrición xenética|transcrición]] de [[splicing alternativo]], que codifican distintas [[isoforma]]s.<ref name="entrez" />
The protein encoded by this gene is a member of the [[protein tyrosine phosphatase]] (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an extracellular domain, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus belongs to receptor type PTP. This gene is specifically expressed in hematopoietic cells. This PTP has been shown to be an essential regulator of T- and B-cell antigen receptor signaling. It functions through either direct interaction with components of the antigen receptor complexes or by activating various Src family kinases required for the antigen receptor signaling. This PTP also suppresses JAK kinases, and, thus, functions as a negative regulator of cytokine receptor signaling. Four alternatively spliced transcripts variants of this gene, which encode distinct isoforms, have been reported.<ref name="entrez" />
 
It is a type I [[transmembrane protein]] that is in various forms present on all differentiated [[hematopoietic]] cells except [[erythrocytes]] and [[plasma cells]] that assists in the activation of those cells (a form of [[co-stimulation]]). It is expressed in [[lymphoma]]s, [[B-cell]] [[chronic lymphocytic leukemia]], [[hairy cell leukemia]], and [[acute nonlymphocytic leukemia]]. A [[monoclonal antibody]] to CD45 is used in routine [[immunohistochemistry]] to differentiate between histological sections from lymphomas and carcinomas.<ref name=Leong>{{cite book|author=Leong, Anthony S-Y|author2=Cooper, Kumarason|author3=Leong, F Joel W-M|year=2003|title=Manual of Diagnostic Cytology|edition=2|publisher=Greenwich Medical Media, Ltd.|pages=121–124|isbn=1-84110-100-1}}</ref>