Sandbox Reserved 162: Difference between revisions

This structure of Interleukin-6 was crystallized at 1.9Å. IL-6 is a monomer of 185 amino acids coded by a gene found at locus 7p21 which codes for four introns and five exons. It contains <scene name='Sandbox_Reserved_162/5_helices/2'>five alpha helices</scene>, four of which constitute a classical four-helix bundle with the fifth helix located in the C-D loop. The four helices that form the four-helix bundle are arranged so that two helices (A & B) run parrallel and two (C & D) in an opposing direction. The N-terminal 18 amino acids of IL-6 are not visible in electron density maps and consequently have not been modeled. The first long helix <scene name='Sandbox_Reserved_162/Helix_a/1'>(A)</scene> extends from Ser21 to Ala45 and is connected to a parallel helix (B) by a 25 amino acid loop. This helix <scene name='Sandbox_Reserved_162/Helix_b/1'>(B)</scene> extends from Glu80 to Gln102. A short connection formed from Asn103 to Ser108 joins this helix to the next helix <scene name='Sandbox_Reserved_162/Helix_c/1'>(C)</scene>. This third helix extends from Glu109 to Lys129 and is followed by another amino acid loop which includes a <scene name='Sandbox_Reserved_162/Helix_e/1'>short helix</scene> of three turns (Pro141-Gln152). The last helix <scene name='Sandbox_Reserved_162/Helix_d/2'>(D)</scene> extends from Gln156 to Arg182<ref>Somers W, Stahl M, Seehra J, "1.9Å crystal structure of interleukin 6: implications for a novel mode of receptor dimerization and signaling."  EMBO J, 1997, 16(5), 989-997.</ref>.  

Interleukin 6 is released in response to infection, burns, trauma, and neoplasia (Citation). Additionally, it is a potent polyfunctional [[Wiktionary:cytokine|cytokine]] that plays a vital role in host defense. This is demonstrated by its ability to induce responses in the immune system, hematopoietic system, and in acute-phase reactions. In the immune system, IL-6 is an essential factor for antibody production in B cells and acts as a potent growth factor for myeloma cells. IL-6 also acts on the final maturation stage of activated B cells, can be effective on resting T cells, and induces differentiation of cytotoxic T cells. In the hematopoietic system, IL-6 (in combination with Interleukin-3) activates and accelarates the growth of hematopoietic stem cells during the G0 phase causing them to enter the G1 phase. With respect to acute-phase reactions, IL-6 plays a key role in enhancing the innate immune system by inducing the expression of mRNA's for proteins associated with acute-phase reactions. These proteins are resleased into blood plasma by liver cells and protect against tissue damage. Moreover, IL-6 is thought to cross the blood brain barrier and induce synthesis of Prostaglandin E2 (PGE2) in the hypothalmus which changes the body's temperature setpoint resulting in fever (Citation).  

As IL-6 plays many parts in the body, research is continually discovering new roles in which it plays. Disregulated production of IL6 and its receptor are implicated in the pathogenesis of many diseases including diabetes, atherosclerosis, depression, Alzheimer's Disease, systemic lupus erythematosus, prostate cancer, rheumatoid arthritis, and multiple myeloma. A good correlation has been found between levels of IL-6 and bone loss in patients with Paget's disease and multiple myeloma. In those patients, higher levels of IL-6 correlated to higher rates of bone loss. Additionally, IL-6 levels decreased with increasing levels of estrogen. These findings strongly suggest that IL-6 plays a key roll in post-menopausal bone loss (Citation). Early research, where bone marrow cells used in transplants were precultured with IL-6 and IL-3, showed an increase in post-transplant cell survival rate from 20% to 90% (Citation). If this culture system can be expanded for human stem cells, it may be used in bone marrow tansplantation (Citation). Other research has indicated that IL-6 is an important factor in malignant cells of Kaposis sarcoma and multiple myelome (Citation).