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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Signal-regulatory_protein_alpha</id>
	<title>Signal-regulatory protein alpha - Revision history</title>
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	<updated>2026-05-02T23:38:48Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wikimd.org/index.php?title=Signal-regulatory_protein_alpha&amp;diff=5379005&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2024-03-10T05:53:08Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Signal-regulatory protein alpha&amp;#039;&amp;#039;&amp;#039; (&amp;#039;&amp;#039;&amp;#039;SIRPα&amp;#039;&amp;#039;&amp;#039;), also known as &amp;#039;&amp;#039;&amp;#039;CD172a&amp;#039;&amp;#039;&amp;#039;, is a protein that in humans is encoded by the &amp;#039;&amp;#039;&amp;#039;SIRPA&amp;#039;&amp;#039;&amp;#039; gene. SIRPα is a member of the signal-regulatory protein (SIRP) family, and also belongs to the immunoglobulin superfamily. SIRPα is expressed predominantly by myeloid cells and is involved in a range of cellular processes such as [[neutrophil]] migration, [[phagocytosis]], and [[cell adhesion]].&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
SIRPα is a transmembrane protein that consists of three immunoglobulin-like domains, a transmembrane region, and a cytoplasmic region that contains two immunoreceptor tyrosine-based inhibition motifs (ITIMs). The extracellular region of SIRPα interacts with [[CD47]], a widely expressed cell surface protein, to prevent phagocytosis.&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
SIRPα plays a crucial role in the regulation of many cellular processes. It is involved in the negative regulation of receptor tyrosine kinase-coupled signaling processes. SIRPα can also induce cell-cell adhesion when it interacts with CD47, which is present on the surface of many cell types. This interaction is important for the prevention of self-phagocytosis.&lt;br /&gt;
&lt;br /&gt;
==Clinical significance==&lt;br /&gt;
Alterations in the expression or function of SIRPα have been implicated in several diseases, including [[cancer]], [[autoimmune diseases]], and [[neurodegenerative diseases]]. In cancer, SIRPα-CD47 interaction can be exploited by cancer cells to evade immune surveillance. Therapies that block this interaction are currently being developed and tested in clinical trials.&lt;br /&gt;
&lt;br /&gt;
==See also==&lt;br /&gt;
* [[CD47]]&lt;br /&gt;
* [[Phagocytosis]]&lt;br /&gt;
* [[Immunoglobulin superfamily]]&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Proteins]]&lt;br /&gt;
[[Category:Immunology]]&lt;br /&gt;
[[Category:Cell biology]]&lt;br /&gt;
[[Category:Medicine]]&lt;br /&gt;
&lt;br /&gt;
{{Protein-stub}}&lt;br /&gt;
{{Medicine-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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