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[Cancer Research 46, 198-202, January 1, 1986]
© 1986 American Association for Cancer Research

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Lack of Development of Thermotolerance in Early Progenitors of Murine Bone Marrow Cells1

Nahid F. Mivechi2 and Gloria C. Li

Radiation Oncology Research Laboratory, CED-200, The University of California, San Francisco, San Francisco, California 94143

We have studied the sensitivities of four hematopoietic stem cell types to heat stress as well as their abilities to develop thermotolerance. Granulocyte-macrophage colony forming units were the most heat resistant bone marrow progenitors tested. Of the erythroid progenitors tested, erythrocyte colony forming units were more resistant than the two more primitive erythrocyte burst forming units.

To determine their ability to develop thermotolerance, hematopoietic precursors were heated in vivo at 43°C for 30 min. At various times thereafter the hematopoietic stem cells were flushed from female C3Hf/Sed mouse preheated tibia. The bone marrow cell suspensions were then heated in vitro and plated for colony formation. The four stem cell precursors differed markedly in their abilities to develop thermotolerance. The thermotolerance induced in granulocyte-macrophage colony forming units reached a maximum at 3–6 h after heating and disappeared by 24–48 h. The thermotolerance in erythrocyte colony forming units (0.5 units erythropoietin/ml media) reached a maximum at 3–6 h and disappeared by 48–72 h. The maximum level of thermotolerance reached by granulocyte-macrophage colony forming units and erythrocyte colony forming units was approximately the same. On the contrary, the two more primitive erythrocyte precursors which were grown by the addition of 2.5 and 5 units erythropoietin/ml of media do not develop thermotolerance.

1 This work was supported by NIH Grant CA-31397.

2 To whom requests for reprints should be addressed.

Received 6/27/85. Revised 10/ 1/85. Accepted 10/ 4/85.




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L. Huang, N. F. Mivechi, and D. Moskophidis
Insights into Regulation and Function of the Major Stress-Induced hsp70 Molecular Chaperone In Vivo: Analysis of Mice with Targeted Gene Disruption of the hsp70.1 or hsp70.3 Gene
Mol. Cell. Biol., December 15, 2001; 21(24): 8575 - 8591.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1986 by the American Association for Cancer Research.