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Most external influences upon cells of any organ are mediated by biochemical and molecular mechanisms that are triggered by interactions with membrane, cytoplasmic, or nuclear receptors. Our understanding of the receptors and the intermediate molecules that couple them with cellular pathways that influence the proliferation, activation, differentiation, or survival of hematopoietic cells has expanded significantly. Proteins on the surface of blood cells that transmit vital information from the extracellular environment include single-pass, homodimeric, heterodimeric, and heterotrimeric transmembrane proteins that do, or do not, contain intrinsic kinase activity, but either way signal by inducing the tyrosine phosphorylation of a multitude of cytoplasmic proteins, seven transmembrane domain proteins that signal through G proteins, heterodimeric integrins that recruit large focal adhesions, and large families of heterodimeric proteins that induce serine and threonine phosphorylation. This chapter describes the receptors that influence blood cell production and function, the secondary mediators and the biochemical modifications they undergo to alert the cell to an external influence, the molecular mechanisms that allow for the coordination of multiple signals impacting a cell simultaneously, and the processes upon which they impact.


Acronyms and Abbreviations:

AP2, adaptor protein-2; BCR, B-cell antigen receptor; BMP, bone morphogenic protein; CNTF, ciliary neurotrophic factor; CT-1, cardiotrophin-1; DD, death domain; DR, death receptor; EPO, erythropoietin; EPOR, erythropoietin receptor; ERK, extracellular response kinase; FADD, Fas-associated death domain; FAK, focal adhesion kinase; G-CSF, granulocyte colony-stimulating factor; Gab, Grb binding; GH, growth hormone; GM-CSF, granulocyte-macrophage colony-stimulating factor; GPCR, G-protein-coupled receptor; HCR, hematopoietic cytokine receptor; IAP, inhibitors of apoptosis; IKK, I-κB kinase; IL, interleukin; IRS, insulin receptor substrate; ITAM, immunoreceptor tyrosine-based activation motif; ITIM, immunoreceptor tyrosine-based inhibitory motif; JAK, Janus family kinase; JNK, c-Jun N-terminal kinase; LIF, leukemia inhibitory factor; M-CSF, macrophage colony-stimulating factor; MAPK, mitogen-activated protein kinase; NR, nuclear receptor; OSM, oncostatin M; PI3K phosphoinositol 3′-kinase; PIAS, protein inhibitor of activated STATs; PIP, phosphoinositol phosphate; PKC, protein kinase C; PTP, protein tyrosine phosphatase; RACK, receptor for activated C kinase; RTK, receptor tyrosine kinase; SARA, SMAD anchor for receptor activation; SCID, severe combined immunodeficiency; SH2, Src homology 2; SOCS, suppressors of cytokine signaling; STATs, signal transducers and activators of transcription; SUMO, small ubiquitin-like modifier; TGF, transforming growth factor; TM, transmembrane; TNF, tumor necrosis factor; TPO, thrombopoietin; TRADD, TNF receptor death domain; TRAF, TNF receptor-associated factor; TRAIL, tumor necrosis factor-related apoptosis-inducing ligand.




Blood cells and their marrow-based progenitors are exquisitely responsive to their environment. A wide variety of cues are detected by mature blood cells that impact significantly on their function. For example, leukocytes respond to noxious stimuli by chemokine-induced migration toward inflammatory stimuli, cross endothelial cell barriers and the extracellular matrix by engaging integrins, and then respond to chemotactic gradients to enter inflammatory foci to contact and engulf microorganisms on encountering bacterial products. Likewise, platelets adhere to reactive endothelial surfaces or denuded subendothelial cell matrix by engagement of extracellular adhesive proteins. Adherent platelets can ...

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