TY - JOUR
T1 - Behavior of p388 mouse leukemia in the chick embryo and hatched chick
AU - Clarkson, Bayard
AU - Katz, Ada
AU - Dann, Mary Ann
AU - Karnofsky, David A.
N1 - Funding Information:
1 Received July 11, 1963. I Supported by grants CY-3192 and CY-3215 from the National Cancer Institute, National Institutes of Health, Public Health Service, and by 8 grant from the American Cancer Society, Inc.
PY - 1964/2
Y1 - 1964/2
N2 - P388 and several other mouse leukemias grow poorly on the chorio-allantoic membrane of the chick embryo, but may proliferate rapidly when introduced into the embryo by intravenous injection, or by metastasis from chorio-allantoic explants. Proliferation of P388 cells in the embryo probably continues until shortly after it has hatched, and then stops; however, viable leukemic cells may persist in the chick brain for as long as 6 weeks after hatching. The brain appears to be the most favorable site for growth and long-term survival of P388 cells. P388 cells injected intravenously or intracerebrally into 1-day-old hatched chicks will survive for long periods, but, when given to 7-day-old and older chicks, the cells fail to survive. This suggests the rapid maturation of immunological competence by the chick shortly after hatching. Marked splenomegaly and hematopoietic stimulation in the embryo may result from injection of P388 and several other mouse leukemias. The splenomegaly is due to proliferation of host cells, particularly the granulocytic elements. The significance of the increased hematopoiesis and splenomegaly and its relation to that reported after the transplantation of homologous adult spleen into the embryo require further study.
AB - P388 and several other mouse leukemias grow poorly on the chorio-allantoic membrane of the chick embryo, but may proliferate rapidly when introduced into the embryo by intravenous injection, or by metastasis from chorio-allantoic explants. Proliferation of P388 cells in the embryo probably continues until shortly after it has hatched, and then stops; however, viable leukemic cells may persist in the chick brain for as long as 6 weeks after hatching. The brain appears to be the most favorable site for growth and long-term survival of P388 cells. P388 cells injected intravenously or intracerebrally into 1-day-old hatched chicks will survive for long periods, but, when given to 7-day-old and older chicks, the cells fail to survive. This suggests the rapid maturation of immunological competence by the chick shortly after hatching. Marked splenomegaly and hematopoietic stimulation in the embryo may result from injection of P388 and several other mouse leukemias. The splenomegaly is due to proliferation of host cells, particularly the granulocytic elements. The significance of the increased hematopoiesis and splenomegaly and its relation to that reported after the transplantation of homologous adult spleen into the embryo require further study.
UR - http://www.scopus.com/inward/record.url?scp=78651197572&partnerID=8YFLogxK
U2 - 10.1093/jnci/32.2.471
DO - 10.1093/jnci/32.2.471
M3 - Article
C2 - 14120161
AN - SCOPUS:78651197572
SN - 0027-8874
VL - 32
SP - 471
EP - 505
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 2
ER -