Abstract
Natural Killer (NK) cells are innate lymphocytes playing pivotal roles in host defense and immune-surveillance. The homeostatic modulation of germ-line encoded/non-rearranged activating and inhibitory NK cell receptors (NKRs) determines the capability of these innate lymphocytes to either spare “self” cells or to kill viral-infected, tumor-transformed and heterologous cell targets. However, despite being discovered more than 40 years ago, several aspects of NK cell biology remain unknown or are still being debated. In particular, our knowledge of human NK cell ontogenesis and differentiation is still in its infancy as the majority of our experimental evidence on this topic mainly comes from findings obtained in vitro or with animal models in vivo. Although both the generation and the maintenance of human NK cells are sustained by hematopoietic stem cells (HSCs), the precise site(s) of NK cell development are still poorly defined. Indeed, HSCs and hematopoietic precursors are localized in different anatomical compartments that also change their ontogenic commitments before and after birth as well as in aging. Currently, the main site of NK cell generation and maturation in adulthood is considered the bone marrow, where their interactions with stromal cells, cytokines, growth factors, and other soluble molecules support and drive maturation. Different sequential stages of NK cell development have been identified on the basis of the differential expression of specific markers and NKRs as well as on the acquisition of specific effector-functions. All these phenotypic and functional features are key in inducing and regulating homing, activation and tissue-residency of NK cells in different human anatomic sites, where different homeostatic mechanisms ensure a perfect balance between immune tolerance and immune-surveillance. The present review summarizes our current knowledge on human NK cell ontogenesis and on the related pathways orchestrating a proper maturation, functions, and distributions.
Highlights
Natural Killer (NK) cells were first described as large granular lymphocytes with a natural ability to kill tumor cells without a previous activation [1]
NK cells remain in a resting state due to the engagement of iNKRs [i.e., inhibitory Killer Immunoglobulin-like receptors, the C-type lectin receptor NKG2A, Ig-like transcripts (ILTs), and the leukocyte Ig-like receptors (LIRs)], that recognize a broad spectrum of classical and non-classical Human Leukocyte Antigen (HLA)-I molecules constitutively expressed of autologous “self ” cells [10, 11]
These cells are widely distributed in several tissues and organs of human body, most of the current knowledge on these innate lymphocytes is limited to peripheral blood (PB-) NK cells [22]
Summary
Natural Killer (NK) cells were first described as large granular lymphocytes with a natural ability to kill tumor cells without a previous activation [1]. ∼10–20% of total lymphocytes in human lungs are NK cells, they share a very similar phenotype with circulating CD56dim NK cell subset and express very low levels of tissueresidency markers.
Published Version (Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have