Response to letter to the editor: “Comments on Unambiguous identification and characterization of a long-term human metabolite of dehydrochloromethyltestosterone”

2018 ◽  
Vol 11 (1) ◽  
pp. 185-185
Author(s):  
Guro Forsdahl ◽  
Thomas Geisendorfer ◽  
Lorenz Göschl ◽  
Sandra Pfeffer ◽  
Peter Gärtner ◽  
...  
2018 ◽  
Vol 10 (8) ◽  
pp. 1244-1250 ◽  
Author(s):  
Guro Forsdahl ◽  
Thomas Geisendorfer ◽  
Lorenz Göschl ◽  
Sandra Pfeffer ◽  
Peter Gärtner ◽  
...  

2007 ◽  
Vol 64 (4) ◽  
pp. 274-287 ◽  
Author(s):  
Matilda A. Haas ◽  
Jyoti A. Chuckowree ◽  
Roger S. Chung ◽  
James C. Vickers ◽  
Tracey C. Dickson

Blood ◽  
2011 ◽  
Vol 118 (2) ◽  
pp. 289-297 ◽  
Author(s):  
Dongdong Ma ◽  
Jing Zhang ◽  
Hui-feng Lin ◽  
Joseph Italiano ◽  
Robert I. Handin

Abstract HSCs are defined by their ability to self-renew and maintain hematopoiesis throughout the lifespan of an organism. The optical clarity of their embryos and the ease of genetic manipulation make the zebrafish (Danio rerio) an excellent model for studying hematopoiesis. Using flow cytometry, we identified 2 populations of CD41-GFP+ cells (GFPhi and GFPlo) in the whole kidney marrow of Tg(CD41:GFP) zebrafish. Past studies in humans and mice have shown that CD41 is transiently expressed in the earliest hematopoietic progenitors and is then silenced, reappearing in the platelet/thrombocyte lineage. We have transplanted flow-sorted GFPhi and GFPlo cells into irradiated adult zebrafish and assessed long-term hematopoietic engraftment. Transplantation of GFPhi cells did not reconstitute hematopoiesis. In contrast, we observed multilineage hematopoiesis up to 68 weeks after primary and secondary transplantation of GFPlo cells. We detected the CD41-GFP transgene in all major hematopoietic lineages and CD41-GFP+ cells in histologic sections of kidneys from transplant recipients. These studies show that CD41-GFPlo cells fulfill generally accepted criteria for HSCs. The identification of fluorescent zebrafish HSCs, coupled with our ability to transplant them into irradiated adult recipients, provide a valuable new tool to track HSC homing, proliferation, and differentiation into hematopoietic cells.


2004 ◽  
Vol 56 (2-3) ◽  
pp. 229-246 ◽  
Author(s):  
Alwynne B. Beaudoin

Abstract The Northern Great Plains region is especially sensitive to drought and is likely to be even more drought-prone under projected global warming. Drought has been invoked as an explanatory factor for changes seen in postglacial paleoenvironmental records. These proxy records may extend drought history derived from instrumental data. Moreover, in the last decade, some paleoenvironmental studies have been expressly undertaken for the examination of long-term drought history. Nevertheless, few such studies explicitly define drought. This makes it difficult to compare results or to understand what the results mean in terms of the operational drought definitions that are used in resource management. Operational drought is defined as usually short-term; longer sustained dry intervals reflect a shift to aridity. Therefore, high resolution paleoenvironmental proxies (annual or subdecadal) are best for the investigation of drought history. Such proxies include tree rings and some lake records. However, most lake-based records are sampled at lower resolution (decadal or subcentury) and are therefore providing aridity signals.


2006 ◽  
Vol 20 (15) ◽  
pp. 2252-2258 ◽  
Author(s):  
Wilhelm Schänzer ◽  
Hans Geyer ◽  
Gregor Fußhöller ◽  
Natalia Halatcheva ◽  
Maxie Kohler ◽  
...  

1999 ◽  
Vol 276 (3) ◽  
pp. F331-F339 ◽  
Author(s):  
David Marples ◽  
Jørgen Frøkiaer ◽  
Søren Nielsen

The discovery of the aquaporin family of water channels has greatly improved our understanding of how water crosses epithelial cells, particularly in the kidney. The study of the mechanisms involved in the regulation of collecting duct water permeability, in particular, has advanced very rapidly since the identification and characterization of aquaporin-2 (AQP2) in 1993. One of the more surprising findings has been the dramatic long-term changes that are seen in the abundance of this protein, as well as the recognition that these changes represent a way of modulating the acute antidiuretic effects of vasopressin. Furthermore, such changes seem to be of etiological and pathological significance in a number of clinical disorders of water balance. This review focuses on the various conditions in which AQP2 expression is altered (either increased or decreased) and on what this can tell us about the signals and mechanisms controlling these changes. Ultimately, this may be of great value in the clinical management of water balance disorders. Evidence is also now beginning to emerge that there are similar changes in the expression of other renal aquaporins, which had previously been thought to provide an essentially constitutive water permeability pathway, suggesting that they too should be considered as regulatory factors in the control of body water balance.


2021 ◽  
Author(s):  
Zanshé Thompson ◽  
Georgina A. Anderson ◽  
Melanie Rodriguez ◽  
Seth Gabriel ◽  
Vera Binder ◽  
...  

Hematopoiesis is tightly regulated by a network of transcription factors and complexes that are required for the development and maintenance of hematopoietic stem cells (HSCs). We recently identified the tumor suppressor, Ing4, as a critical regulator of HSC homeostasis. Though the Ing4 mechanism of action remains poorly characterized, it has been shown to promote stem-like cell characteristics in malignant cells. This activity is, in part, due to Ing4 mediated regulation of several major signaling pathways, including NF-kB and c-Myc. In murine hematopoiesis, Ing4 deficiency induces G0 arrest in HSCs, while simultaneously promoting gene expression signatures associated with differentiation. This results in a poised state for Ing4-deficient HSCs. Long term HSCs are unable to overcome this block, but short-term HSCs convert the poised state into regenerative capacity during hematopoietic challenges, including irradiation and transplantation. Overall, our findings suggest that Ing4 plays a crucial role in the regulation of hematopoiesis. Our model provides key tools for further identification and characterization of pathways that control quiescence and differentiation in HSCs.


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