Chronobiology in hematology and immunology

Abstract

The hematopoietic and the immune systems in all their components are characterized by a multifrequency time structure with prominent rhythms in cell proliferation and cell function in the circadian, infradian, and rhythms in cell proliferation and cell function in the circadian, infradian, and circannual frequency ranges. The circulating formed elements in the peripheral blood show highly reproducible circadian rhythms. The timing and the extent of these rhythms were established in a clinically healthy human population and are shown as chronograms, cosinor summaries and, for some high-amplitude rhythms, as time-qualified reference ranges (chronodesms). Not only the number but also the reactivity of circulating blood cells varies predictably as a function of time as shown for the circadian rhythm in responsiveness of human and murine lymphocytes in vitro to lectin mitogens (phytohemagglutinin and pokeweed mitogen). Some circadian rhythms of hematologic functions appear to be innate and are presumably genetically determined but are modulated and adjusted in their timing by environmental factors, so-called synchronizers. Phase alterations in the circadian rhythms of hematologic parameters of human subjects and of mice by manipulation of the activity-rest or light-dark schedule and/or of the time of food uptake are presented. Characteristically these functions do not change their timing immediately after a shift in synchronizer phase but adapt over several and in some instances over many transient cycles. The circadian rhythm of cell proliferation in the mammalian bone marrow and lymphoid system as shown in mice in vivo and in vitro may lend itself to timed treatment with cell-cycle-specific and nonspecific agents in an attempt to maximize the desired and to minimize the undesired treatment effects upon the marrow. Differences in response, and susceptibility of cells and tissues at different stages of their circadian and circaseptan (about 7-day) rhythms and presumably of cyclic variations in other frequencies are expected to lead to the development of a chronopharmacology of the hematopoietic and immune system. Infradian rhythms of several frequencies have been described for numerous hematologic and immune functions. Some of these, i.e., in the circaseptan frequency range, seem to be of importance for humoral and for cell mediated immune functions including allograft rejection. Infradian rhythms with periods of 19 to 22 days seem to occur in some hematologic functions and are very prominent in cyclic neutropenia and (with shorter periods) in its animal model, the grey collie syndrome.(ABSTRACT TRUNCATED AT 400 WORDS)

Administration Time–Dependent Effects of Aspirin on Blood Pressure in Untreated Hypertensive Patients

“…The hypothesis that a time-dependent effect of ASA on thromboxane production could also be at least partly responsible for the time-dependent effects of ASA on BP gains some relevancy given the lack of any effect of ASA on HR (Figure 3). Taking into account the administration timedependent BP lowering by ASA, relevant studies have also shown statistically significant circadian rhythms in thromboxane and prostacyclin production, 32 circulating platelets, 33 platelet aggregation, 32,34,35 clotting and fibrinolytic inhibitors, 32 and in the inhibition of platelet aggregation produced by ASA. 15 On the other hand, ASA has also been shown not only to restore vascular refractoriness to angiotensin II 36 but also to produce a dose-dependent BP reduction and Ͼ30% inhibition of angiotensin II.…”

Immunometabolism: Is it under the eye of the clock?

“…The number of haematopoeietic stem and progenitor cells (HSPCs) and mature leukocytes peak in the blood during the resting phase in mice [58], while levels of proinflammatory cytokines including IL-1␤ and TNF peak during the active phase [57,59]. In mice leukocytes reach their highest numbers in blood at zeitgeber time (ZT) 5 but their greatest recruitment to tissues is at ZT13 [60].…”

The Adult Hematopoietic Niches — Cellular Composition, Histological Organization and Physiological Regulation

“…The mobilization from BM is dependent on local sympathetic innervation which down-regulates the CXCL12 expression in the BM in close association with a reduced CXCR4 expression of haematopoietic progenitors [99] and both CD4+and CD8+T cell subsets [94]. On the contrary, the onset of the active phase is related to a peak of glucocorticoids, adrenaline, noradrenaline, TNF and IL1β [95,96].…”

“…The haematopoietic system exhibits circadian rhythms that oscillate according to the rest-activity phase that, by turn, depend on whether the species is diurnal or nocturnal. Thus, the numbers of HSCs, committed progenitor cells and most mature leukocytes, except CD8+T lymphocytes [94] peak in the circulation during the resting phase (night for humans and day for rodents) and decrease during the active period [95,96].…”