4.6 Article

The Role of LNK (SH2B3) in the Regulation of JAK-STAT Signalling in Haematopoiesis

Journal

PHARMACEUTICALS
Volume 15, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/ph15010024

Keywords

JAK-STAT; myeloproliferative neoplasms

Funding

  1. National Health and Medical Research Council (NHMRC) in Australia [1122999, 1113577]
  2. NHMRC IRIISS [9000220]
  3. Victorian State Government Operational Infrastructure Scheme
  4. Cancer Council Victoria [1183557]
  5. NHMRC fellowship
  6. HSANZ Leukaemia Foundation Scholarship
  7. National Health and Medical Research Council of Australia [1122999] Funding Source: NHMRC

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LNK is an adaptor protein that regulates cytokine signaling and constrains the activation of the JAK-STAT pathway. Mutations in LNK can lead to increased signaling and contribute to various hematological and inflammatory diseases.
LNK is a member of the SH2B family of adaptor proteins and is a non-redundant regulator of cytokine signalling. Cytokines are secreted intercellular messengers that bind to specific receptors on the surface of target cells to activate the Janus Kinase-Signal Transducer and Activator of Transcription (JAK-STAT) signalling pathway. Activation of the JAK-STAT pathway leads to proliferative and often inflammatory effects, and so the amplitude and duration of signalling are tightly controlled. LNK binds phosphotyrosine residues to signalling proteins downstream of cytokines and constrains JAK-STAT signalling. Mutations in LNK have been identified in a range of haematological and inflammatory diseases due to increased signalling following the loss of LNK function. Here, we review the regulation of JAK-STAT signalling via the adaptor protein LNK and discuss the role of LNK in haematological diseases.

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