Purity
>90%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Level
<0.10 EU per 1 μg of the protein by the LAL method.
Activity
Measured by the ability of the immobilized protein to support the adhesion of SVEC4‑10 mouse vascular endothelial cells. The ED 50 for this effect is 0.1-0.5 μg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived Gln27-Asn963, with a C-terminal 6-His tag
Accession #
N-terminal Sequence
AnalysisGln27 predicted: No results obtained, sequencing might be blocked
Predicted Molecular Mass
104.4 kDa
SDS-PAGE
120-145 kDa, reducing conditions
7860-TH |
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Formulation Lyophilized from a 0.2 μm filtered solution in PBS. | ||
Reconstitution Reconstitute at 200 μg/mL in PBS. | ||
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. | ||
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Background: Thrombospondin-4
Thrombospondin-4 (TSP-4) is an approximately 140 kDa matricellular protein that is secreted as a disulfide-linked pentamer. Within the Thrombospondin family, TSP‑3 and TSP‑5/COMP are also pentameric, while TSP‑1 and TSP‑2 are trimeric. TSP‑4 regulates cell‑cell and cell matrix interactions and plays a role in cardiovascular physiology and neuronal development (1, 2). Mature mouse TSP‑4 consists of an N‑terminal heparin-binding domain, a coiled coil motif, four EGF‑like repeats, seven TSP type‑3 repeats (one with an RGD motif), and a TSP C‑terminal domain (2, 3). Mouse TSP‑4 shares 93% and 97% amino acid sequence identity with human and rat TSP‑4, respectively. TSP‑4 binds a variety of matrix proteins including Collagens I, II, III, V, Laminin‑1, Fibronectin, and Matrilin‑2 (4). Interactions of TSP‑4 with non‑collagenous proteins are independent of divalent cations, whereas interactions with collagenous proteins are enhanced in the presence of zinc (4). TSP‑4 binds to cell surface Integrins containing the alpha M, beta 2, or beta 3 chains (5, 6). It is expressed in skeletal muscle and tendon as well as by vascular smooth muscle and endothelial cells (7‑9). It is up‑regulated in cardiomyocytes during pressure overload and is required for mediating the responsive increase in cardiac contractility (10). In humans, a polymorphism of TSP-4 (A387P) is associated with myocardial infarction (11). TSP-4 contributes to the development of inflammation and atherosclerosis by promoting macrophage and neutrophil adhesion to the vasculature (5, 6). In the nervous system, TSP‑4 is expressed by astrocytes and neurons and is enriched at neuromuscular junctions and synapse‑rich layers of the brain and retina (9, 12, 13). It promotes neuronal adhesion, neurite outgrowth, and excitatory synaptogenesis (9, 13, 14). TSP‑4 is up‑regulated in the spinal cord following peripheral nerve injury where it contributes to presynaptic hypersensitivity and hyperalgesia (12). It is also up‑regulated in muscle following denervation (9). TSP‑4 is additionally secreted by tumor‑associated fibroblasts in gastric adenocarcinoma, particularly in regions of tumor cell invasion (15).
References:
Murphy-Ullrich, J.E. and R.V. Iozzo (2012) Matrix Biol. 31:152.
Lawler, J. et al. (1995) J. Biol. Chem. 270:2809.
Newton, G. et al. (1999) Mamm. Genome 10:1010.
Narouz-Ott, L. et al. (2000) J. Biol. Chem. 275:37110.
Pluskota, E. et al. (2005) Blood 106:3970.
Frolova, E.G. et al. (2010) Circ. Res. 107:1313.
Sodersten, F. et al. (2007) Connect. Tiss. Res. 48:254.
Stenina, O.I. et al. (2003) Circulation 108:1514.
Arber, S. and P. Caroni (1995) J. Cell Biol. 131:1083.
Cingolani, O.H. et al. (2011) Circ. Res. 109:1410.
Stenina, O.I. et al. (2007) Arterioscler. Thromb. Vasc. Biol. 27:1886.
Kim, D.-S. et al. (2012) J. Neurosci. 32:8977.
Dunkle, E.T. et al. (2007) Exp. Eye Res. 84:707.
Eroglu, C. et al. (2009) Cell 139:380.
Forster, S. et al. (2011) Mod. Pathol. 24:1390.
Entrez Gene IDs:
7060 (Human); 21828 (Mouse)
Alternate Names:
THBS4; thrombospondin 4; Thrombospondin4; Thrombospondin-4; TSP4; TSP-4
