• Purity

  >95%, 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 its ability to inhibit apoptosis on the J774A.1 mouse reticulum cell sarcoma macrophage cells. Miyazaki, T.     et al. (1999) J. Exp. Med.     189:413. The presence of rhCD5L inhibited rhFas Ligand induced apoptosis by 70-90%. The ED    ₅₀ for this effect is 1-4 μg/mL.

• Source

  Mouse myeloma cell line, NS0-derived Ser20-Gly347, with a C-terminal 6-His tag

• Accession #

• N-terminal Sequence    
  Analysis

  Ser20

• Predicted Molecular Mass

  36.9 kDa

• SDS-PAGE

  43 kDa, reducing conditions

Background: CD5L

CD5L (CD5 antigen-like), also known as Sp alpha and AIM, is a 50 kDa secreted glycoprotein that belongs to the SRCR (scavenger receptor cysteine rich) group B family of proteins. Group B proteins are distinguished by SRCR domains that are encoded by a single exon (1 - 3). The human CD5L cDNA encodes a 347 amino acid (aa) precursor that includes a 19 aa signal sequence and three SRCR domains (4, 5). Among group B proteins, CD5L is most closely related to CD5 and CD6, with which it shares 18% and 31% aa sequence identity, respectively. CD5L is up-regulated in macrophages at inflammatory sites. It sustains inflammatory reactions by both increasing the phagocytic capacity of macrophages and impeding the apoptosis of local macrophages, NK cells, and T cells (6, 7). Agonists of the LXR and RXR nuclear hormone receptors induce CD5L upregulation in macrophages and reduce macrophage apoptosis (8, 9). Oxidized LDL (which acts through LXR/RXR) is taken up by macrophages, promoting their development into foam cells. The increased level of CD5L protects foam cells from apoptosis but permits more rapid cellular accumulation and atherosclerotic plaque formation (9). In activated B cells, however, the combination of CD5L and TGF-beta inhibits proliferation. The binding of CD5L to splenic B cells is increased following TGF-beta exposure, suggesting that TGF-beta increases the expression or availability of an unidentified CD5L receptor (5, 10). CD5L also functions as a pattern recognition molecule by binding both lipoteichoic acid on Gram positive and lipopolysaccharide on Gram negative bacteria (11). In the thymic cortex, CD5L protects cortical CD4⁺CD8⁺ thymocytes from apoptosis (12). CD5L circulates in the serum in complex with IgM (13).

• References:

1. Sarrias, M.R. et al. (2004) Crit. Rev. Immunol. 24:1.

2. Resnick, D. et al. (1994) Trends Biochem. Sci. 19:5.

3. Mukhopadhyay, S. and S. Gordon (2004) Immunobiology 209:39.

4. Gebe, J.A. et al. (1997) J. Biol. Chem. 272:6151.

5. Gebe, J.A. et al. (2000) Immunol. 99:78.

6. Haruta, I. et al. (2001) J. Biol. Chem. 276:22910.

7. Kuwata, K. et al. (2003) Am. J. Pathol. 162:837.

8. Valledor, A.F. et al. (2004) Proc. Natl. Acad. Sci. 101:17813.

9. Arai, S. et al. (2005) Cell Metab. 1:201.

10. Yusa, S. et al. (1999) Eur. J. Immunol. 29:1086.

11. Sarrias, M-R. et al. (2005) J. Biol. Chem. 280:35391.

12. Miyazaki, T. et al. (1999) J. Exp. Med. 189:413.

13. Tissot, J.D. et al. (2002) Electrophoresis 23:1203.

• Long Name:

  CD5 Antigen-like

• Entrez Gene IDs:

  922 (Human); 11801 (Mouse)

• Alternate Names:

  AIM; API6; apoptosis inhibitor 6; CD5 antigen-like (scavenger receptor cysteine rich family); CD5 antigen-like; CD5 molecule-like; CD5L; CT-2; IgM-associated peptide; PRO229; Spalpha; SP-alpha