Adult somatic stem cells (SSCs) are self-renewing groups of cells in tissues and organs that can produce specific lineages of precursor cells leading to differentiated cell progeny. They are retained from organogenesis throughout life for cell maintenance, repair and regeneration [1] . During differentiation SSCs are established in unique cell/ECM niches. Niches are tissue specific sites in vivo consisting of differentiated cells that modulate stem cells. The niche histological composition varies extensively in different tissues but often includes stromal cells, extracellular matrix, blood vessels, neurons and tissue related precursor differentiated cells [2] . The stem cell population is often a mixture of quiescent stem cells (or active stem cells) and progenitor cells in various levels of differentiation. The surrounding niche cells regulate stem and progenitor cells and serve both as a specific topographical and functional site [3,4,5] . SSCs are often multipotent and their lineage leads to uni-potent progenitors for terminal differentiated cells. Activated stem cells divide symmetrically to produce identical cells for self-renewal. Alternatively, an asymmetric cell division produces a reserve stem cell and a cytoplasmic partitioned progenitor cell committed to a specific pathway. Where there is a cyclic demand for somatic cell renewal, short lived, intermediate transit amplifying (TA) cells proliferate extensively before differentiation into adult cells [4,5] . The resident population of diverse progenitors is possibly recruited and selected for their developmental potential to meet a specific function. The niche modulates stem cell function needed to maintain physiological needs for homeostasis and organismic variations in growth, maturation, reproduction and senescence that can alter stem/progenitor behavior [6] . Stem cells and their progeny within the niche may also be transient rather than fixed and adaptable to unusual conditions during tissue homeostasis or trauma