Hrk/DP5 contributes to the apoptosis of select neuronal populations but is dispensable for haematopoietic cell apoptosis. 2007

Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, Victoria 3050, Australia.

The pro-apoptotic BH3-only members of the Bcl2 family, crucial initiators of cell death, are activated by a diverse array of developmental cues or experimentally applied stress stimuli. We have investigated, through gene targeting in mice, the biological roles for the BH3-only family member HRK (also known as DP5) in apoptosis regulation. Hrk gene expression was found to be restricted to cells and tissues of the central and peripheral nervous systems. Sensory neurons from mice lacking Hrk were less sensitive to apoptosis induced by nerve growth factor (NGF) withdrawal, consistent with the induction of Hrk following NGF deprivation. By contrast, cerebellar granule neurons that upregulate Hrk upon transfer to low-K+ medium underwent apoptosis normally under these conditions in the absence of Hrk. Furthermore, loss of Hrk was not sufficient to rescue the neuronal degeneration in lurcher mutant mice. Despite previous reports, no evidence was found for Hrk expression or induction in growth-factor-dependent haematopoietic cell lines following withdrawal of their requisite cytokine, and haematopoietic progenitors lacking HRK died normally in response to cytokine deprivation. These results demonstrate that HRK contributes to apoptosis signalling elicited by trophic factor withdrawal in certain neuronal populations but is dispensable for apoptosis of haematopoietic cells.

UI MeSH Term Description Entries
D008810 Mice, Inbred C57BL One of the first INBRED MOUSE STRAINS to be sequenced. This strain is commonly used as genetic background for transgenic mouse models. Refractory to many tumors, this strain is also preferred model for studying role of genetic variations in development of diseases. Mice, C57BL,Mouse, C57BL,Mouse, Inbred C57BL,C57BL Mice,C57BL Mice, Inbred,C57BL Mouse,C57BL Mouse, Inbred,Inbred C57BL Mice,Inbred C57BL Mouse
D008818 Mice, Neurologic Mutants Mice which carry mutant genes for neurologic defects or abnormalities. Lurcher Mice,Nervous Mice,Reeler Mice,Staggerer Mice,Weaver Mice,Chakragati Mice,Chakragati Mouse,Lurcher Mouse,Mice, Neurological Mutants,Mouse, Neurologic Mutant,Mouse, Neurological Mutant,Nervous Mouse,Neurologic Mutant Mice,Neurological Mutant Mouse,Reeler Mouse,Staggerer Mouse,Weaver Mouse,ckr Mutant Mice,Mice, Chakragati,Mice, Lurcher,Mice, Nervous,Mice, Neurologic Mutant,Mice, Reeler,Mice, Staggerer,Mice, Weaver,Mice, ckr Mutant,Mouse, Chakragati,Mouse, Lurcher,Mouse, Nervous,Mouse, Reeler,Mouse, Staggerer,Mouse, Weaver,Mutant Mice, Neurologic,Mutant Mice, ckr,Mutant Mouse, Neurologic,Neurologic Mutant Mouse
D009420 Nervous System The entire nerve apparatus, composed of a central part, the brain and spinal cord, and a peripheral part, the cranial and spinal nerves, autonomic ganglia, and plexuses. (Stedman, 26th ed) Nervous Systems,System, Nervous,Systems, Nervous
D009474 Neurons The basic cellular units of nervous tissue. Each neuron consists of a body, an axon, and dendrites. Their purpose is to receive, conduct, and transmit impulses in the NERVOUS SYSTEM. Nerve Cells,Cell, Nerve,Cells, Nerve,Nerve Cell,Neuron
D009479 Neuropeptides Peptides released by NEURONS as intercellular messengers. Many neuropeptides are also hormones released by non-neuronal cells. Neuropeptide
D002531 Cerebellum The part of brain that lies behind the BRAIN STEM in the posterior base of skull (CRANIAL FOSSA, POSTERIOR). It is also known as the "little brain" with convolutions similar to those of CEREBRAL CORTEX, inner white matter, and deep cerebellar nuclei. Its function is to coordinate voluntary movements, maintain balance, and learn motor skills. Cerebella,Corpus Cerebelli,Parencephalon,Cerebellums,Parencephalons
D005727 Ganglia, Spinal Sensory ganglia located on the dorsal spinal roots within the vertebral column. The spinal ganglion cells are pseudounipolar. The single primary branch bifurcates sending a peripheral process to carry sensory information from the periphery and a central branch which relays that information to the spinal cord or brain. Dorsal Root Ganglia,Spinal Ganglia,Dorsal Root Ganglion,Ganglion, Spinal,Ganglia, Dorsal Root,Ganglion, Dorsal Root,Spinal Ganglion
D006412 Hematopoietic Stem Cells Progenitor cells from which all blood cells derived. They are found primarily in the bone marrow and also in small numbers in the peripheral blood. Colony-Forming Units, Hematopoietic,Progenitor Cells, Hematopoietic,Stem Cells, Hematopoietic,Hematopoietic Progenitor Cells,Cell, Hematopoietic Progenitor,Cell, Hematopoietic Stem,Cells, Hematopoietic Progenitor,Cells, Hematopoietic Stem,Colony Forming Units, Hematopoietic,Colony-Forming Unit, Hematopoietic,Hematopoietic Colony-Forming Unit,Hematopoietic Colony-Forming Units,Hematopoietic Progenitor Cell,Hematopoietic Stem Cell,Progenitor Cell, Hematopoietic,Stem Cell, Hematopoietic,Unit, Hematopoietic Colony-Forming,Units, Hematopoietic Colony-Forming
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D016207 Cytokines Non-antibody proteins secreted by inflammatory leukocytes and some non-leukocytic cells, that act as intercellular mediators. They differ from classical hormones in that they are produced by a number of tissue or cell types rather than by specialized glands. They generally act locally in a paracrine or autocrine rather than endocrine manner. Cytokine

Related Publications

Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
October 2007, The Journal of biological chemistry,
Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
June 2008, Journal of cell science,
Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
September 2010, Blood,
Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
February 2022, G3 (Bethesda, Md.),
Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
November 2009, Cell death and differentiation,
Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
December 2005, Neurobiology of disease,
Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
September 1997, Genes & development,
Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
July 2009, Molecular microbiology,
Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
March 2013, Molecular and cellular biology,
Leigh Coultas, and Susanna Terzano, and Tim Thomas, and Anne Voss, and Kate Reid, and Edouard G Stanley, and Clare L Scott, and Philippe Bouillet, and Perry Bartlett, and Jonathan Ham, and Jerry M Adams, and Andreas Strasser
January 2010, Oncogene,
Copied contents to your clipboard!