T. Terashima et al., POLYMORPHONUCLEAR LEUKOCYTE TRANSIT TIMES IN BONE-MARROW DURING STREPTOCOCCAL PNEUMONIA, American journal of physiology. Lung cellular and molecular physiology, 15(4), 1996, pp. 587-592
The release of polymorphonuclear leukocytes (PMN) from the bone marrow
(BM) is a hallmark of acute inflammatory conditions. BM stimulation m
ay increase the toxic potential of these newly released PMN and influe
nce their behavior at inflammatory sites. The present study was design
ed to measure the transit time of PMN in the mitotic and postmitotic p
ools of the BM in rabbit using 5'-bromo-2'-deoxyuridine (BrdU). Blood
samples were obtained at 2- to 24-h intervals from 24 to 192 h after a
single BrdU injection, and BrdU-positive PMN (PMN(BrdU)) was detected
as they appear in the circulating blood, using immunohistochemistry.
The intensity of nuclear staining for BrdU was used to define a single
generation of PMN and graded as either weakly (G1), moderately (G2),
or highly (G3) stained. The mean +/- SE transit time of PMN(BrdU) thro
ugh the BM was 95.6 +/- 3.6 h, with 51.1 +/- 5.9 h in the mitotic and
65.4 +/- 5.4 h in the postmitotic pool. Streptococcus pneumoniae insti
llation in the lung(n = 3) shortened the transit time of PMN through t
he BM to 54.0 +/- 2.6 h with a shorter time in both the mitotic (36.2
+/- 5.7 h) and the postmitotic pool (34.6 +/- 0.8 h). All these values
were shorter than the control values (P < 0.05). We conclude that Str
eptococcus pneumoniae shortens the transit time of PMN in the mitotic
and postmitotic pools in the marrow, which may result in the release o
f immature PMN with higher levels of lysosomal enzymes into the circul
ation.