S. Vaneeden et al., L-SELECTIN EXPRESSION INCREASES ON PERIPHERAL-BLOOD POLYMORPHONUCLEARLEUKOCYTES DURING ACTIVE MARROW RELEASE, American journal of respiratory and critical care medicine, 151(2), 1995, pp. 500-507
Citations number
37
Categorie Soggetti
Emergency Medicine & Critical Care","Respiratory System
The cell adhesion molecule L-selectin is highly expressed on mature bo
ne marrow polymorphonuclear leukocytes (PMN), and the release of these
cells from the bone marrow could produce a population of circulating
PMN expressing high levels of L-selectin. Because L-selectin initiates
the interaction of PMN with activated endothelium, these cells could
be important in the pathogenesis of multiorgan failure following sepsi
s and septic shock. The present study was designed to test the hypothe
sis that the release of PMN from the bone marrow increases the express
ion of L-selectin on circulating PMN. Peripheral blood and bone marrow
samples were obtained immediately after sternotomy(BM1) and during (B
M2) and just before closing the sternum (BM3) in five normothermic and
five hypothermic cardiopulmonary bypass (CPB) procedures. L-selectin
was measured using both immunocytochemistry and flow cytometry. The re
sults showed that L-selectin expression on bone marrow PMN was greater
than on peripheral blood PMN (p < 0.01) in all patients at baseline.
Bone marrow release of PMN during normothermic CPB was associated with
a rise in peripheral blood band cells (0.18 +/- 0.7 versus 2.98 +/- 0
.56 x 10(9)/L) (p < 0.01) and an increase in the percentage of PMN exp
ressing high levels of L-selectin (9 +/- 3.3 to 36 +/- 6.6%, p < 0.03)
and the L-selectin mean fluorescence intensity (MFI) on PMN (p < 0.05
). The expression of L-selectin on band cells was higher than on segme
nted PMN in the circulation (p < 0.01). Hypothermia (27 degrees C) pre
vented the release of band cells into the circulation and the increase
d expression of L-selectin on the PMN. We conclude that PMN released f
rom the bone marrow express high levels of L-selectin and speculate th
at these newly released PMN may be preferentially recruited to inflamm
atory sites.