کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2202812 1100395 2013 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Semaphorin7A and its receptors: Pleiotropic regulators of immune cell function, bone homeostasis, and neural development
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Semaphorin7A and its receptors: Pleiotropic regulators of immune cell function, bone homeostasis, and neural development
چکیده انگلیسی

Semaphorins form a large, evolutionary conserved family of cellular guidance signals. The semaphorin family contains several secreted and transmembrane proteins, but only one GPI-anchored member, Semaphorin7A (Sema7A). Although originally identified in immune cells, as CDw108, Sema7A displays widespread expression outside the immune system. It is therefore not surprising that accumulating evidence supports roles for this protein in a wide variety of biological processes in different organ systems and in disease. Well-characterized biological effects of Sema7A include those during bone and immune cell regulation, neuron migration and neurite growth. These effects are mediated by two receptors, plexinC1 and integrins. However, most of what is known today about Sema7A signaling concerns Sema7A–integrin interactions. Here, we review our current knowledge of Sema7A function and signaling in different organ systems, highlighting commonalities between the cellular effects and signaling pathways activated by Sema7A in different cell types. Furthermore, we discuss a potential role for Sema7A in disease and provide directions for further research.


► Sema7A regulates cell proliferation, differentiation, migration and maturation.
► The biological effects of Sema7A are mediated by plexinC1 and integrin receptors.
► Sema7A–plexinC1 and Sema7A–integrin interaction have opposing effects on cell adhesion.
► Abnormal expression and function of Sema7A is linked to disease and injury.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Seminars in Cell & Developmental Biology - Volume 24, Issue 3, March 2013, Pages 129–138
نویسندگان
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