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Notes: Recently we reported that the deep cortex of the rat lymph node is made up of semi-rounded “units,” some of which are partially fused into “complexes”. We further found that each unit is centered on the opening(s) of an afferent lymphatic vessel, the topographical organization of the deep cortex of a node correlating with the distribution pattern of the opening(s) of its afferent lymphatic(s). The present study aims to clarify the morphology of the deep cortex unit, particularly with regard to its reticular framework, its lymphatic sinuses, as well as its network of postcapillay venules. For that purpose, we analyzed rat nodes from various locations by way of tridimensional reconstruction. The observations revealed that each unit is formed of a “center” and a “periphery,” distinguishable from one another on the basis of their morphological features. The center is nearly devoid of reticular fibers, whereas the periphery exhibits a dense framework of fibers. Moreover, the periphery is the site of concentration of most postcapillary venules of a unit and contains lymphatic sinuses which, peculiarly, are often loaded with small lymphocytes. While both regions are populated mainly by small lymphocytes, the periphery usually contains a lower concentration of these cells than the center. The overall findings support the view that the center is a site of cellular retention and proliferation, whereas the periphery is a site of rapid lymphocyte migration in and out of the unit.

Notes: Using tridimensional reconstruction, it was recently found that the deep cortex of rat lymph nodes comprises one to several basic “units”. Each unit is a semi-rounded structure contiguous to the peripheral cortex and bulging into the medulla of a node. Other investigators reported that transfused lymphocytes, heavily labelled in vitro by 3H-uridine, became concentrated in an illdefined region of nodes, referred to as the mid and deep cortex. This suggested to us that the in vivo labelling of nodes with 3H-uridine, might allow to further characterize the units on a physiological basis. Therefore, rats were injected intraveously with a dose of 1-20 μCi of 3H-uridine/gm body weight and sacrificed 1 hour to 3 days later. The radioautographs of their nodes were exposed up to 535 days. The observations revealed that a large dose of 3H-uridine combined with a long exposure of the radioautographs yielded a differntial labelling of the cell population of the units, characterized by a much more intense reaction than that of the surrounding structures. This demonstrated that the physiology of the lymphocyte population of the deep cortex units differs from the morphologically similar lymphocyte population of the extrafollicular zone of the peripheral cortex. The possible reason(s) for the differential labelling of the units is discussed.

Notes: Recently, we reported that the deep cortex of the rat lymph node is formed of semi-rounded structures, the “deep cortex units,” contiguous to the peripheral cortex and bulging into the medulla. It was suggested that a unit represents an accumulation of lymphocytes centered on the opening of an afferent lymphatic vessel. To verify the proposal, we carried out a tridimensional analysis of serially sectioned rat nodes, fixed by perfusion and trimmed in such a way as to preserve their lymphatics. The tridimensional analysis revealed that a constant topographical relationship exists between the units and the openings of the afferent lymphatics. The results demonstrated that the topographical organization of the deep cortex of a rat node correlates with the distribution pattern of the opening(s) of its afferent lymphatic(s). The overall observations suggested the following explanation for the shape and topography of the units: factor(s) present in the lymph would spread in a radial manner from the opening(s) of an afferent lymphatic through the underlying cortex. The factor(s) would induce morphological modifications in the stimulated semi-rounded area which, in turn, would provoke a local accumulation of circulating lymphocytes.

Notes: In preceeding studies, we clarified the histology of the deep cortex of the rat lymph node. It was shown that the deep cortex is made up of basic elements termed “deep cortex units,” some of which are fused to one another into “deep cortex complexes.” Each unit is a semirounded lymphocytic structure, centered on the opening of an afferent lymphatic, contiguous to the peripheral cortex, and bulging into the medulla of a node. Moreover, each unit comprises a “center” and a “periphery,” bearing distinct morphological features. The present work was undertaken to verify whether the histology of the deep cortex of nodes from various species of mammals, currently used for experimental immunology, is comparable to that of the rate. The observations yielded a positive answer to the question.

Notes: The deep cortex of the lymph node of various species actually consists of hemispherical structures, termed deep cortex “units.” Each unit is centered under an opening of an afferent lymphatic and comprises a center and a periphery. In a recent work on the nude mouse, we found that the congenital athymic state inhibits the development of the lymphocyte population in the center of the units as well as in a related area of peripheral cortex, and that it also modifies other nodal components. In the present work, we wanted to compare the effects of the athymic state on the rat nodes. Therefore, nodes from various anatomical locations in 8-week-old nude rats were submitted to a tridimensional analysis. The overall effects of the congenital athymic state were found to be comparable in rats and mice. However, marked differences were noticed in the modifications of the node histology, in both species of nude animals. Their significance is discussed together with new findings.

Notes: Diagrams of the lymph node currently represent its deep cortex (paracortex) as a layer of rather uniform thickness underlying the whole peripheral cortex. However, this concept has not been supported by actual observations; previous nvestigators have observed, instead, related structures whose appearance varied greatly from nodule-like to ill-defined components. Clearly, the present knowledge of the histology of the deep cortex is inadequate and confusing. Therefore, we undertook a tridimensional study of the region in different nodes of rats. The present work, bearing on the topography of the region, revealed that the deep cortex of the rat node is formed of one to several basic “units”. Each unit is a semi-rounded structure, varying from semispheric to semi-ovoid in shape and contiguous to a portion of peripheral cortex. The work further showed that two to several units can fuse to form a “complex”. The data indicated that the number, the size and the shape of the units and/or of the complexes of a node differ to some extent according to its anatomical location. These differences probably reflect corresponding variations in the nature and importance of the antigenic stimulation in the different sites of the organism. Finally, the study demonstrated the necessity of tridimensional examination of a node to obtain adequate information on its overall architecture and, particularly, on its deep cortex topography.

Notes: ABSTRACT Recently, the deep cortex of the adult rat lymph node was shown to be made up of semirounded lymphocytic “units.” Each unit is contiguous to the peripheral cortex, bulges into the medulla, and is centered on the opening(s) of an afferent lymphatic vessel of a node. Furthermore, each unit comprises a “center” and a “periphery,” bearing distinct morphological features. The present study investigated the postnatal development of the units in rats of various ages. One minute after birth, no lymphocytic structures were detected in the nodes. One day after birth, tiny rounded lymphocytic areas were detected in the developing cortex. These areas were topographically related to the openings of afferent lymphatic vessels. One week after birth, small semirounded lymphocytic areas with some morphological features of the adult deep cortex units were observed. Two weeks after birth, typical units were present in the nodes. The observations indicated that the rounded lymphocytic areas observed in nodes of rats aged 1 week or less were actually developing deep cortex units. The overall findings further provided information on the morphological processes involved during the postnatal development of the deep cortex units. Key words: lymph node, deep cortex, development of deep cortex, rat.

Notes: The immunogenic content of the afferent lymph stimulates structures in the lymph node. Thus, a better knowledge of the processes of lymph flow and filtration in the organ should help us better understand various aspects of the node's function. To gain this understanding, we analyzed the distribution of flow in rat node draining areas locally injected with a small dose of China ink. Because the lymph-flow pattern is likely related to the overall architecture of the node, we simultaneously studied its morphology. Indeed, while the different structures of the node are known, some aspects of its overall architecture need to be resolved. The present work aimed to accomplish this by an analysis of semiserial sections of nodes from various anatomical locations in normal rats; the sections were stained by the Dominici technique or silver-impregnated.With respect to their architecture, the nodes could be distinguished into those with either a discontinuous or a continuous subcapsular sinus and peripheral cortex. These are referred to here, respectively, as segmented and nonsegmented nodes. In the segmented nodes, the subcapsular sinus with the peripheral cortex is separated by “gaps,” in which medullary sinuses reached the capsule. Further, a node appears to be divided into one or more “physiological compartments,” each one representing a nodal area related to an opening of an afferent lymphatic.The findings on China-ink distribution indicate that the lymph-flow pattern varies in different nodes and is determined by the particular architecture of a node, i.e., the lymph flow in a given node aligns itself along the pattern of segmentation of the organ. The findings suggest that the lymph content is first held by the endothelium lining the inner wall of a restricted area of the subcapsular sinus in a concentration which decreases with the distance from the related afferent lymphatic opening. Part of the content, possibly its nonimmunogenic fraction, would later be released to flow further along the sinus. It would then be phagocytosed by the macrophage accumulation located in the portions of medullary sinuses into which the lymph enters from the subcapsular sinus. The lymph thus filtered then flows along the medullary sinuses and leaves the organ. The latter findings also indicate that a node is divided into physiological compartments, each one being stimulated by the lymph from a given afferent lymphatic opening. As the immunogenic content of the lymph can differ from one lymphatic to another, this explains the frequent variations in similar structures located in different areas of a given node. Hence, the pattern of distribution of the openings of the afferent lymphatics of a node can account for the particularities of its overall architecture and its division into physiological compartments.