ATOMIC MEDICINE

it became evident that age, strain and species were factors that influenced

the results. The effectiveness of several subcellular fractions of spleen

homogenates prepared by the Schneider-Hogeboom techniques was then
tested. The experiments conclusively showed that there was no restorative
effect connected with the mitochondria, microsomes or soluble supernatant fractions. The restorative effect was found only with the cell meleus
fraction. Since relatively few intact cells were found on stained smears of
the nucleus fraction, it was believed that their experiments strongly sup-

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were common.

A British group (Barnes and Loutit) have made a series of contributions
on the nature of the restorative action of splenic implants and homogenates.
Initially, they confirmed the effectiveness of splenic homogenates. Next,
they showed that immunization of one strain of mouse (CBA) bystrain A
material prevents protection; whereas, short-lived protection of CBA mice
could be obtained by use of strain A material in nonimmune mice. In
general, their experience was the same as Cole ef al. in that freezing, thawing, irradiation, and formalin-treatment inactivated the principle. Their
studies, extensively confirmed for bone marrow, showed that the restorative principle of intact CBA mice spleens could be preserved when the
spleens are equilibrated with glycerol serum andstored at —70°C. for as
long as 83 days.
Recently very signifieant studies, incantrovertible when con-idered together, have been reported independently by several different laboratories

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have shown that DN Aase and trypsin inactivate the material, as does
distilled water extraction under various conditions. Since enzymes are
believed not to attack living intact cells, these experiments were interpreted as indicating that the active principle is associated with DNA
and not necessarily with living cells. These contentions argued strongly
for the noncellular concept.
It was thought carly that studies with heterologous marrow might provide the definitive answer to the question of whether cell transfer is involved in these protective phenomena. Lorenz and Congdon, and Congdon
and Lorenz reported that homologous and heterologous ground bone favorably modify lethal radiation injury in the mouse. Transplanted homologous
bone developed bone marrow, but heterologous bone transplants did not
show bone marrowformation. The same investigators reported protection of
some strains of mice by intravenous injections of rat bone marrow emulsion
from certain strains of rats. They interpreted the bone and bone marrow
transplant studies as evidence in favorof the existence of a humoral factor.
Cole et al. protected mice with rat bone marrow. Late deaths after 2 weeks

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ported the concept that the restorative effect was noncellular and associated with the nucleoproteins. Further studies on the splenic homogenates

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