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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Integrin alpha 9

integrin alpha9
Top mentioned proteins: CAN, p63, V1a, Tenascin, ITGA9
Papers on integrin alpha9
MicroRNA-125b suppresses the epithelial-mesenchymal transition and cell invasion by targeting ITGA9 in melanoma.
Qiu et al., Nanchang, China. In Tumour Biol, Dec 2015
Furthermore, our findings demonstrate that upregulating miR-125b significantly inhibits malignant phenotypes by repressing the expression of integrin alpha9 (ITGA9).
Integrin α9β1 in airway smooth muscle suppresses exaggerated airway narrowing.
Sheppard et al., San Francisco, United States. In J Clin Invest, 2012
integrin alpha9beta1 appears to serve as a brake on airway smooth muscle contraction by recruiting SSAT, which facilitates local catabolism of polyamines and thereby inhibits PIP5K1gamma.
EMILIN1-α4/α9 integrin interaction inhibits dermal fibroblast and keratinocyte proliferation.
Spessotto et al., Italy. In J Cell Biol, 2011
EMILIN1 is identified as a novel ligand for keratinocyte alpha9beta1 integrin, suggesting prospective roles for this receptor-ligand pair in skin homeostasis.
Characterization and safety assessment of bioengineered limbal epithelium.
Zubaidah et al., Kuala Lumpur, Malaysia. In Med J Malaysia, 2011
Cultivated cells were positive for p63, K3, K19, and involucrin but negative for K14, integrin alpha9 and ABCG2 when analyzed by immunohistochemistry. Expression of molecular markers was detectable with real-time RT-PCR.
Integrin alpha9 (ITGA9) expression and epigenetic silencing in human breast tumors.
Grigorieva et al., Novosibirsk, Russia. In Cell Adh Migr, 2011
Integrin alpha9 (ITGA9) is one of the less studied integrin subunits that facilitates accelerated cell migration and regulates diverse biological functions such as angiogenesis, lymphangiogenesis, cancer cell proliferation and migration.
Rab11 and its effector Rab coupling protein contribute to the trafficking of beta 1 integrins during axon growth in adult dorsal root ganglion neurons and PC12 cells.
Fawcett et al., Cambridge, United Kingdom. In J Neurosci, 2010
Expression of the tenascin-C-binding integrin alpha9 promotes axon regeneration.
ADAM2 interactions with mouse eggs and cell lines expressing α4/α9 (ITGA4/ITGA9) integrins: implications for integrin-based adhesion and fertilization.
Evans et al., Baltimore, United States. In Plos One, 2009
data indicate that ITGA9-ITGB7 functions as an ADAM binding partner in certain cellular contexts, with implications for mammalian fertilization and integrin function
The integrin alpha9beta1 on hematopoietic stem and progenitor cells: involvement in cell adhesion, proliferation and differentiation.
Klein et al., Tübingen, Germany. In Haematologica, 2009
Cell-cell adhesion assays with osteoblasts and dye-labeled CD34(+) hematopoietic stem and progenitor cells in the presence of function-blocking antibodies revealed a role of integrin alpha9 in hematopoietic stem and progenitor cell adhesion to osteoblasts.
Integrin-alpha9 is required for fibronectin matrix assembly during lymphatic valve morphogenesis.
Makinen et al., London, United Kingdom. In Dev Cell, 2009
Results reveal an important role for integrin-alpha9 signaling during lymphatic valve morphogenesis and implicate it as a candidate gene for primary lymphedema caused by valve defects.
Alpha9 integrin and its ligands constitute critical joint microenvironments for development of autoimmune arthritis.
Uede et al., Sapporo, Japan. In J Immunol, 2009
Inhibition of alpha(9) integrin function with an anti-alpha(9) integrin Ab significantly reduces the production of arthrogenic cytokines and chemokines and ameliorates ongoing arthritis
Integrin alpha9beta1 mediates enhanced cell migration through nitric oxide synthase activity regulated by Src tyrosine kinase.
Vlahakis et al., Rochester, United States. In J Cell Sci, 2009
A novel and unique mechanism of coordinated interactions of the integrin alpha9 cytoplasmic domain, Src tyrosine kinase and iNOS to transduce integrin-alpha9beta1-mediated cell migration.
Reduction of mouse egg surface integrin alpha9 subunit (ITGA9) reduces the egg's ability to support sperm-egg binding and fusion.
Evans et al., Baltimore, United States. In Biol Reprod, 2009
Reduction of mouse egg surface integrin alpha9 subunit (ITGA9) reduces the egg's ability to support sperm-egg binding and fusion.
Loss of integrin alpha9beta1 results in defects in proliferation, causing poor re-epithelialization during cutaneous wound healing.
Van De Water et al., Albany, United States. In J Invest Dermatol, 2009
alpha9beta1 is crucial for efficient and proper re-epithelialization during cutaneous wound healing
Prox1 induces lymphatic endothelial differentiation via integrin alpha9 and other signaling cascades.
Miyazono et al., Tokyo, Japan. In Mol Biol Cell, 2007
Here, we show that Prox1, via induction of integrin alpha9 expression, inhibits sheet formation and stimulates motility of endothelial cells.
Cultivation of human corneal limbal stem cells in Mebiol gel--A thermo-reversible gelation polymer.
Abraham et al., Chennai, India. In Indian J Med Res, 2006
The cultivated cells expressed the presumed limbal stem cell association markers (ABCG2 and p63), the transient amplifying cell markers (connexin 43, integrin alpha9) and the cornea differentiation marker (K3).
Limbal stem cells: the search for a marker.
Wiffen et al., Australia. In Clin Experiment Ophthalmol, 2006
Many markers such as p63 and integrin alpha9 are preferentially localized to the limbus but cannot be regarded as stem cell-specific.
Identification and characterization of limbal stem cells.
Kruse et al., Erlangen, Germany. In Exp Eye Res, 2005
Data reported from the literature combined with our own recent observations suggest, that the basal epithelial cells of the human limbus contain ABCG2, K19, vimentin, KGF-R, metallothionein, and integrin alpha9, but do not stain for K3/K12, Cx43, involucrin, P-cadherin, integrins alpha2, alpha6, and beta4, and nestin, when compared to the basal cells of the corneal epithelium.
The lymphangiogenic vascular endothelial growth factors VEGF-C and -D are ligands for the integrin alpha9beta1.
Sheppard et al., San Francisco, United States. In J Biol Chem, 2005
VEGF-C and VEGF-D are ligands for the integrin alpha9beta1
Spermidine/spermine N1-acetyltransferase specifically binds to the integrin alpha9 subunit cytoplasmic domain and enhances cell migration.
Sheppard et al., San Francisco, United States. In J Cell Biol, 2004
The integrin alpha9beta1 is expressed on migrating cells, such as leukocytes, and binds to multiple ligands that are present at sites of tissue injury and inflammation.
Generation and characterization of telomerase-transfected human lymphatic endothelial cells with an extended life span.
Pepper et al., Genève, Switzerland. In Am J Pathol, 2004
hTERT-HDLEC also express the recognized lymphatic markers, Prox-1, LYVE-1 and podoplanin, as well as integrin alpha9, but do not express CD34.
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