Relationship of normal CDF1 mouse leukocyte kinetics to growth characteristics of leukemia L1210.

نویسندگان

  • V T DeVita
  • C Denham
  • S Perry
چکیده

SUMMARY Leukocyte kinetics were studied in the CDF1 mouse using liquid scintillation and radioautographic technics. Although the latter method provides more detailed information, the former technic is readily adaptable-to experimental manipula tions. The kinetics of mouse leukocytes are different from those in man. Either marrow storage and transit times are different or the generation times of mouse marrow progenitor cells is shorter. Data presented in this study and those available in the literature support the latter concept. The selective thera peutic advantage of the mouse marrow cells is probably related to the presence of nonproliferating cells inaccessible to chemo therapy as reported in the literature. Knowledge of both nor mal and tumor cell kinetics is essential if drug scheduling is to be placed on a more rational basis.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

In vivo DNA cross-linking by cyclophosphamide: comparison of human chronic lymphatic leukemia cells with mouse L1210 leukemia and normal bone marrow cells.

Alkaline elution was done on a variety of cells following cyclophosphamide (CY) treatment in vivo. Cells used were L1210 leukemia, normal mouse bone marrow, and peripheral blood cells obtained from a patient with chronic lymphatic leukemia (CLL). Endpoints used were determination of single strand breaks, DNA-DNA interstrand and DNA-protein cross-links. After treatment of mice with CY (4 mg/mous...

متن کامل

Antibiotic binding to human polymorphonuclear neutrophils, mouse leukemia L1210 cells and mouse thymocytes.

This report describes a system in which antibiotics could be compared for binding to different mammalian cells. These included functional phagocytes (human polymorphonuclear neutrophils; PMNs), non-phagocytic lymphocytes (mouse thymocytes), and non-functional leukocytes (mouse leukemia L1210 cells). When antibiotics bound to PMNs, they bound about the same to L1210 cells but much less to thymoc...

متن کامل

Chemotherapeutic Effects on Mammalian Tumor Cells. Ii. Biologic and Chromosomal Instability of a Cyclophosphamide-treated Murine Leukemia.

growth kinetics and karyotype of L1210 leukemia in mice has recently been reported (2). Leukemia sublines, de veloped from tumor cells surviving maximally sublethal treatment with cyclophosphamide, manifested a prolonged generation time, and cytogenetic studies demonstrated highly significant alterations. These findings have been confirmed (unpublished data) using a DBA-carried L1210 line in DB...

متن کامل

In the preceding paper, the development of a Miracil D-resistant sublime of mouse leukemia L1210 has been described (3). In view of its biologic stability and other characteristics, it was of interest to inquire into reasons

D-resistant sublime of mouse leukemia L1210 has been described (3). In view of its biologic stability and other characteristics, it was of interest to inquire into reasons for the failure of this subline to respond to this agent. The present experiments were designed to affirm or eliminate one possible mechanism of resistance (cf. Ref. 4), i.e., reduced uptake of Miracil D by the resistant cell...

متن کامل

Resistance to L1210 mouse leukemia cells in moderately protein-malnourished BALB/c mice treated in vivo with thymosin fraction V.

Moderate protein malnutrition retarded the i.p. proliferation of L1210 mouse leukemia cells in BALB/c mice. The increased resistance against leukemia cell growth in protein-malnourished mice was correlated with increased in vitro mitogenic responsiveness of spleen lymphocytes to phytohemagglutinin and increased levels of serum corticosterone but could not be correlated with altered development ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Cancer research

دوره 29 5  شماره 

صفحات  -

تاریخ انتشار 1969