TY - JOUR
T1 - Receptor tyrosine kinases and the regulation of hematopoiesis
AU - Paulson, Robert F.
AU - Bernstein, Alan
N1 - Funding Information:
We would like to thank members of the Bernstein laboratory for stimulating discussions, and Amy Paulson for excellent editorial help. Work in the Bernstein laboratory is supported by grants from the National Cancer Institute of Canada, the Medical Research Council of Canada, and Bristol-Myers Squibb. A.B. is an International Research Scholar of the Howard Hughes Medical Institute. R.F.P. is a David C. Rae Memorial Fellow of the Leukemia Research Fund of Canada.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1995
Y1 - 1995
N2 - The ongoing production of mature blood cells during the lifetime of an animal is vital for survival. Hematopoesisis the complex process whereby a small population of pluripotential stem cells give rise to mature cell types with specialized functions. The development of mature blood cells proceeds in a hierarchical fashion originating from a self-renewable stem cell population that gradually becomes committed to lineage-restricted differentiation. Two major themes concerning the regulation of hematopoiesis have emerged. First, the proliferation, survival and differentiation of immature progenitor cells depends on extracellular signals produced by cells within the hematopoietic microenvironment. Second, protein tyrosine phosphorylation is the major biochemical mechanism by which the extracellular signals are transmitted and interpreted. In this review we will concentrate on the role of receptors with intrinsic tyrosine kinase activity (RTKs) in hematopoietic regulation. RTKs form part of a highly conserved signaling mechanism that plays an important role in the development of evolutionary diverse organisms. During hematopoiesis, RTKs are a central component of the mechanism by which hematopoietic stem cells receive extracellular signals and interpret these signals to direct the lineage restricted differentiation of multipotential progenitors. In addition, RTKs may also play an important regulatory role in the ontogeny of the hematopoietic system during embryonic and fetal development. Taken together, RTKs are an important component of the mechanisms that regulate the development and behavior of hematopoietic stem cells.
AB - The ongoing production of mature blood cells during the lifetime of an animal is vital for survival. Hematopoesisis the complex process whereby a small population of pluripotential stem cells give rise to mature cell types with specialized functions. The development of mature blood cells proceeds in a hierarchical fashion originating from a self-renewable stem cell population that gradually becomes committed to lineage-restricted differentiation. Two major themes concerning the regulation of hematopoiesis have emerged. First, the proliferation, survival and differentiation of immature progenitor cells depends on extracellular signals produced by cells within the hematopoietic microenvironment. Second, protein tyrosine phosphorylation is the major biochemical mechanism by which the extracellular signals are transmitted and interpreted. In this review we will concentrate on the role of receptors with intrinsic tyrosine kinase activity (RTKs) in hematopoietic regulation. RTKs form part of a highly conserved signaling mechanism that plays an important role in the development of evolutionary diverse organisms. During hematopoiesis, RTKs are a central component of the mechanism by which hematopoietic stem cells receive extracellular signals and interpret these signals to direct the lineage restricted differentiation of multipotential progenitors. In addition, RTKs may also play an important regulatory role in the ontogeny of the hematopoietic system during embryonic and fetal development. Taken together, RTKs are an important component of the mechanisms that regulate the development and behavior of hematopoietic stem cells.
UR - http://www.scopus.com/inward/record.url?scp=0029349179&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0029349179&partnerID=8YFLogxK
U2 - 10.1006/smim.1995.0031
DO - 10.1006/smim.1995.0031
M3 - Article
C2 - 8520031
AN - SCOPUS:0029349179
SN - 1044-5323
VL - 7
SP - 267
EP - 277
JO - Seminars in Immunology
JF - Seminars in Immunology
IS - 4
ER -