Cytokines are involved in many functions  of the immune system including initiating, amplifying and resolving immune  responses. Through bioinformatics analyses of a comprehensive database of gene  expression (BIGE: Body Index of Gene Expression) we observed that a small  secreted protein encoded by a poorly characterized gene called meteorin-like  (METRNL), is highly expressed in mucosal tissues, skin and activated  macrophages. Further  studies indicate that Metrnl is produced by Alternatively  Activated Macrophages (AAM) and M-CSF cultured bone marrow macrophages (M2-like  macrophages). In the skin, METRNL is expressed by resting fibroblasts  and IFNγ-treated  keratinocytes. A screen of human skin-associated diseases showed significant  over-expression of METRNL in psoriasis, prurigo nodularis,  actinic keratosis and atopic dermatitis.   METRNL is  also up-regulated in synovial membranes of human rheumatoid arthritis. Taken  together, these results indicate that Metrnl represents a novel cytokine,  which is likely involved in both innate and acquired immune responses.
    Ushach I, Burkhardt AM, Martinez C et al., Clin Immunol. 2014 Dec 5;156(2):119-127. doi: 10.1016/j.clim.2014.11.006. [Epub ahead of print] 
  
  
  
    Exercise  training benefits many organ systems and offers protection against metabolic  disorders such as obesity and diabetes. Using the recently identified isoform  of PGC1-α (PGC1-α4) as a discovery tool, we report the identification of meteorin-like  (Metrnl), a  circulating factor that is induced in muscle after exercise and in adipose  tissue upon cold exposure. Increasing circulating levels of Metrnl  stimulates energy expenditure and improves glucose tolerance and the expression  of genes associated with beige fat thermogenesis and anti-inflammatory  cytokines. Metrnl  stimulates an eosinophil-dependent increase in IL-4 expression and promotes  alternative activation of adipose tissue macrophages, which are required for  the increased expression of the thermogenic and anti-inflammatory gene  programs in fat. Importantly, blocking Metrnl actions in vivo significantly  attenuates chronic cold-exposure-induced alternative macrophage activation and thermogenic gene  responses. Thus, Metrnl  links host-adaptive responses to the regulation of energy homeostasis  and tissue inflammation and has therapeutic potential for metabolic  and inflammatory diseases. 
    Rao RR, Long JZ, White JP et al., Cell. 2014 Jun 5;157(6):1279-91. doi: 10.1016/j.cell.2014.03.065. 
  
  
  
    AIMS: 
      Adipose  tissue releases adipokines that  play important roles in metabolic and cardio-cerebro-vascular  homeostasis. This study was to discover novel adipokines  using caloric restriction model.
      METHODS: 
      Adipokine  candidates were captured by gene array and bioinformatics analysis and verified  by preparation of recombinant protein and antibody.
      RESULTS: 
      We  established a potential secreted protein database containing 208 genes and  identified a novel adipokine, Subfatin,  that was the  highest expressed in subcutaneous fat of both rodents and humans among 15  detected tissues. The secreted mammalian Subfatin was a glycosylated protein. Subfatin was  located diffusely throughout the adipose tissue except lipid droplets, with  comparable expression between adipocytes and stromal cells, but much lower  expression in macrophages than adipocytes. Subfatin was downregulated in  white adipose tissue of caloric restriction rats, whereas dramatically upregulated  during white adipocyte differentiation as well as in white adipose tissue of  diet-induced obese mice. Subfatin was  annotated as Meteorin-like  (Metrnl) in  public databases, a similar transcript of Meteorin (Metrn, also known as glial cell  differentiation regulator). Meteorin displayed a brain-specific  expression and was scarce in various adipose tissues, in contrast to the tissue  expression patterns of Subfatin.
      CONCLUSIONS: 
      Subfatin is a  novel adipokine  regulated by adipogenesis and  obesity, with tissue distribution different from its homologue Meteorin.
    Li ZY, Zheng SL, Wang P, et al., CNS Neurosci Ther. 2014 Apr;20(4):344-54. doi: 10.1111/cns.12219. Epub 2014 Jan 7.   
  
  
  
    BACKGROUND:
      The  pax2/5/8 genes belonging to the PAX family of transcription factors are key  developmental regulators that are involved in the patterning of various  embryonic tissues. More particularly, their function in inner ear specification  has been widely described. However, little is known about the direct downstream  targets and, so far, no global approaches have been performed to identify these  target genes in this particular tissue.
      RESULTS:
      Here  we present an original bioinformatics pipeline composed of comparative  genomics, database querying and text mining tools, which is designed to rapidly  and specifically discover PAX2/5/8 direct downstream targets involved in inner  ear development. We provide evidence supported by experimental validation in medaka fish  that brain 2 (POU domain, class 3, transcription factor 2), claudin-7,  secretory pathway component sec31-like and meteorin-like precursor  are novel direct downstream targets of PAX2/5/8.
      CONCLUSIONS:
      This  study illustrates the power of extensive mining of public data repositories  using bioinformatics methods to provide answers for a specific biological  question. It furthermore demonstrates how the usage of such a combinatorial  approach is advantageous for the biologist in terms of experimentation time and  costs.
    Ramialison M, Bajoghli B, Aghaallaei N et al., Genome Biol. 2008 Oct 1;9(10):R145. doi: 10.1186/gb-2008-9-10-r145.   
  
 
  
    

Courtesy by Dr. Dun, Temple University
