Juxtacrine signalling

In biology, juxtacrine signalling (or contact-dependent signalling) is a type of cell / cell or cell / extracellular matrix signalling in multicellular organisms that requires close contact. Hence, this stands in contrast to releasing a signaling molecule by diffusion into extracellular space, or the use of long-range conduits like membrane nanotubes and cytonemes (akin to 'bridges'), or the use of extracellular vesicles like exosomes or microvesicles (akin to 'boats'). There are three types of juxtacrine signaling: In biology, juxtacrine signalling (or contact-dependent signalling) is a type of cell / cell or cell / extracellular matrix signalling in multicellular organisms that requires close contact. Hence, this stands in contrast to releasing a signaling molecule by diffusion into extracellular space, or the use of long-range conduits like membrane nanotubes and cytonemes (akin to 'bridges'), or the use of extracellular vesicles like exosomes or microvesicles (akin to 'boats'). There are three types of juxtacrine signaling: Additionally, in unicellular organisms such as bacteria, juxtacrine signaling refers to interactions by membrane contact. The term 'juxtacrine' was originally introduced by Anklesaria et al. (1990) to describe a possible way of signal transduction between TGF alpha and EGFR. Juxtacrine signaling has been observed for some growth factors, cytokine and chemokine cellular signals, playing an important role in the immune response. It has a critical role in development, particularly of cardiac and neural function. Other types of cell signaling include paracrine signalling and autocrine signalling. In this type of signaling, a cell places a specific ligand on the surface of its membrane, and subsequently another cell can bind it with an appropriate cell surface receptor or cell adhesion molecule. An important example is the Notch signaling pathway, notably involved in neural development. Two adjacent cells can construct communicating conduits between their intracellular compartments: gap junctions in animals and plasmodesmas in plants. Gap junctions are made of connexins in vertebrates and innexins in invertebrates. Electrical synapses are electrically conductive gap junctions between neurons. Gap junctions are critical for cardiac myocytes, mice and humans deficient in a particular gap junction protein have severe heart development defects. The extracellular matrix is composed of glycoproteins (proteins and mucopolysaccharides (glycosaminoglycan)) produced by the organism's cells. They are secreted not only to build a supportive structure but also to provide critical information on the immediate environment to nearby cells. Indeed, the cells can themselves interact by contact with extracellular matrix molecules and as such, this can be considered an indirect cell / cell communication. Cells use mainly the receptor integrin to interact with ECM proteins. This signaling can influence the cell cycle and cellular differentiation. In addition to releasing signaling molecules into their environment to initiate quorum sensing, bacteria can use contact-dependent signaling through different mechanisms, for such purpose as to inhibit their growth in harsh conditions.