[20] suggested that distinct monocytic subsets are recruited from the blood at different phases of tissue damage. The latter mechanism of recruitment has also been supported by other studies within the lung.[22, 23] In addition to the two main mouse monocyte subsets, Sunderkötter et al.[17] reported a third subset of monocytes in the peripheral blood with intermediate Ly6C expression, Ly6Cmed. Although not as well studied and characterized in mice, Ly6Cmed monocytes may mature from Ly6Chi monocytes and adopt a similar inflammatory phenotype.[17] Compared with the two main monocyte subsets, Ly6Cmed monocytes may have a greater tendency to migrate to draining lymph nodes and differentiate into DCs.[24] Activation

selleck screening library of monocyte-derived macrophages leads to the production of pro-inflammatory cytokines, chemokines and mediators that kill intracellular pathogens, an important role in host defence. Macrophages play a pivotal role in the removal of dying cells often exacerbating inflammation resulting in tissue destruction and scarring. However, there is now sufficient evidence of macrophage heterogeneity in all stages of inflammation and tissue remodelling. In particular the wound healing and anti-fibrotic role of macrophages that is associated with tissue repair in the kidney,[25-28]

lung,[29] brain,[30] skin,[31, 32] liver,[33] heart,[34] gastrointestinal tract[35] and skeletal muscle.[21, 36, 37] Navitoclax cell line Macrophages adapt to their surrounding microenvironment by displaying a wide variety Bay 11-7085 of phenotypes associated with tissue damage and repair.[38] Local microenvironmental cues essentially shape macrophage

heterogeneity. These can markedly influence the function and polarization of infiltrating and tissue-resident macrophages in response to injury or repair by expressing various cytokines and chemokines, surface markers and microbial products. Although the precise definition of macrophage subpopulations is unclear, they can be separated into two subclasses with opposing polarization states; a classically activated M1-like state and an alternatively activated M2-like state.[39] Because of the distinct functional pathways and gene expression profiles, several classification systems have been postulated for macrophage activation.[40-42] However, essentially these subclasses define macrophages based on in vitro studies following exposure to various stimuli, and thus overlook the complex functional interplay that typically exists in vivo (Table 2).[42, 43] In effect, macrophages most likely represent extremes of a continual spectrum of activated phenotypes rather than discrete stable subsets. Following infiltration into tissues via transmigration across the vascular endothelium, monocytes differentiate into either macrophages or DCs depending upon the influence of a number of factors including adhesion molecules, chemokines and their receptors, and cytokines.