scholarly journals Structural and functional units of parenchyma of lymph nodes of drometaries (Camelus dromedarius)

2017 ◽  
Vol 8 (3) ◽  
pp. 232-333 ◽  
Author(s):  
P. N. Gavrilin ◽  
O. G. Gavrilina ◽  
V. V. Brygadyrenko ◽  
D. E. Rahmoun
Keyword(s):  
Lymph Node ◽  
Connective Tissue ◽  
Lymph Nodes ◽  
B Lymphocytes ◽  
Lymphatic Vessels ◽  
Cell Interaction ◽  
Type I ◽  
Clonal Proliferation ◽  
Relative Capacity ◽  
Cell Cell

This article analyzes patterns of structural and functional organization of the parenchyma of different groups of lymph nodes, structural features of their connective tissue frame and lymphatic sinuses. We studied superficial and deep somatic (Limphonodi mandibulares, L. cervicales superficiales, L. axillares proprii, L. poplitei), somatovisceral (L. retropharyngei mediales, L. iliaci mediales), visceral (L. mediastinales caudales, L. jejunales) features of mature male drometaries (Camelus dromedarius Linnaeus, 1758). We used a complex of traditional macroscopic and histological techniques, and also immunohistochemical staining of lymph node sections for identifying the features of localization of T- and B-lymphocyte populations in the parenchyma of the nodes. We found that the parenchyma of camels’ lymph nodes is characterized by a spongy type structure in the form of a complex of partly concrescent round-oval fragments of lymphoid tissue, surrounded by large lymphatic spaces (sinuses). The connective tissue frame of the lymph nodes is represented by a two-layer (connective tissue-muscular) capsule and two types of trabeculae: two-layered (connective-muscular, type I), which contain blood and lymphatic vessels, as well as lymphatic cysternas, and a single-layered, formed only by a smooth muscular system (type II). Intranodal lymphatic sinuses are subdivided into subcapsular, peritrabecular and medullary sinuses. The subcapsular sinuses and sinuses related to trabeculae of type I and their branching are the most developed. At the tissue level, the lymph node parenchyma has a clearly manifested lobular structure. Lymphoid lobules in the lymph node parenchyma are positioned diffusely (mosaically) and consist of four main cellular zones: transit and cell-cell interaction (analogous to the cortical plateau), clonal proliferation of T- and, respectively, B-lymphocytes (deep cortex units, lymphatic nodules), accumulation of plasmocytes and synthesis of antibodies (brain cords). The lymphoid lobes (compartments) of the lymph nodes parenchyma are bipolar, their tops formed by the zones of transit and cell-cell interaction, and also by the zones of proliferation of B lymphocytes, and the bases by a complex of brain cords (zone of accumulation of plasmocytes and synthesis of antibodies). The zone of T-lymphocytes proliferation is in intermediate position and underlies the subunits of the parenchyma. The tops of the lymphoid lobes are located along the sinuses of the trabeculae of type I and the bases along the sinuses of the trabeculae of type II, which form the efferent lymphatic vessels. The maximum relative capacity of all studied lymph nodes was typical for zones of plasmocyte accumulation and synthesis of antibodies (19–27%), the minimum capacity was typical for transit and cell-cell interaction zones (3–8%). The relative capacity of zones of clonal proliferation of T- and B-lymphocytes in most lymph nodes was 1.5–3.0 times less than that of the zone of plasmocyte accumulation and antibody formation and was, respectively, 8–16% and 9–18%. The study showed that the structure of the lymph nodes parenchyma of drometaries is not absolutely unique. As in other mammal species, it is subdivided into specialized cell zones which are connected in lymphoid lobules. Specific features of parenchyma structure include: diffuse (mosaic) location of lymphoid lobules; absence of signs of regulated localization of lymphoid lobules relative to the capsule and the sinus bordering the nodes. 

scholarly journals Гистоархитектоника паренхимы лимфатических узлов млекопитающих с различными типами строения внутриузлового лимфатического русла

2017 ◽  
Vol 7 (3) ◽  
pp. 96-107 ◽  
Author(s):  
P.N. Gavrilin ◽  
E.G. Gavrilina ◽  
V.V. Evert
Keyword(s):  
T Lymphocytes ◽  
Lymph Nodes ◽  
B Lymphocytes ◽  
Relative Volume ◽  
Type I ◽  
Type Ii ◽  
Lymphatic Channel ◽  
Histological Techniques ◽  
Clonal Proliferation ◽  
Medullary Cords

<p>The article analyzes the features of the histoarchitectonics of the lymph nodes of the bull (Bos taurus) and the pig (Sus scrofa domestica), depending on the type of structure and localization of the intranodal lymphatic channel. We studied somatic (Limphonodi (L.) cervicales superficiales) and visceral (L. jejunales) lymph nodes of clinically healthy mature male bulls and swine (16 and 6 months old, respectively). A complex of classical histological techniques was used, as well as the method of impregnating sections of lymph nodes with silver nitrate, modified by the authors. The main accumulative-distribution link in the lymph nodes of the bull is the subcapsular sinus (type I lymphatic collector), and in the lymph nodes of the pig - the capsular (intratrabecular) lymphatic tanks (type II lymphatic colector). In nodes with collectors of type I, the cortex has a simple layered structure, its outer layer is formed by a compact cortical plateau (interfollicular zone), and the inner layer is formed by a complex of spherical units of the deep cortex. In nodes with collectors of type II, the cortex is layered-folded, uneven in width. Cortical folds are formed along the capsular trabeculae with intratrabecular lymphatic tanks. The cortex plateau in the layered-folded cortex is more developed at the base of the folds, and the units of the deep cortex are at their apexes, where they form clusters in the form of specific nest-shaped structures. In nodes, regardless of the type of intranodal lymphatic channel, the surface cortex (cortical plateau) is located directly under the underlying lymphatic collectors, repeating their shape, the zones of clonal proliferation of B-lymphocytes are formed along the main collector on the basis of cortical plateau and its derivative structures (on the basis of paracortical and medullary cords). The zones of proliferation of T-lymphocytes are maximally close to the main collector, separated from it by a strip of cortical plateau, form a complex of spherical thickenings, which together form a deep cortex. The stroma and parenchyma are more developed in the nodes with collectors of type II (cumulative relative volume of stroma – 9-14% and 6-10%, parenchyma – 80-87% and 70-81%, respectively), and lymphatic sinuses - in nodes with collectors of I type (13-20% and 4-6% respectively). In the parenchyma of the lymph nodes of both groups, the zones of proliferation of T-lymphocytes predominate (the centers of deep cortex units are 27-42%), as well as the zones of accumulation of plasma cells and antibody formation (medullary cords – 17-29%), the first of which are more developed in the pig, and the latter at the nodes of the bull. The cumulative relative volume of the interfollicular zone (cortical plateau) in the studied nodes does not exceed 6-11%, and the zone of clonal proliferation of B lymphocytes (lymph nodulus) is 5-14%. These zones are more developed in the lymph nodes of the pig. Paracortical cords have the minimum and practically equivalent relative volume in the nodes of both groups (3-5%). The study shows that the principles of localization of the main specialized cellular zones in the lymph nodes of the domestic bull and the pig are universal, and the histoarchitectonics of the parenchyma has a clearly expressed specificity. Features of the histoarchitectonics of the parenchyma and its quantitative characteristics are determined by the type of structure of the intranodal lymphatic channel (the character of the localization and spatial configuration of the main accumulative-distributive unit of the nodes). </p>

scholarly journals Tumor Microenvironment of Metastasis (TMEM) Doorways Are Restricted to the Blood Vessel Endothelium in Both Primary Breast Cancers and Their Lymph Node Metastases

Cancers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1507 ◽  
Author(s):  
Ginter ◽  
Karagiannis ◽  
Entenberg ◽  
Lin ◽  
Condeelis ◽  
...  
Keyword(s):  
Breast Cancer ◽  
Lymph Node ◽  
Tumor Microenvironment ◽  
Lymph Nodes ◽  
Lymph Node Metastases ◽  
Lymphatic Vessels ◽  
Breast Tumors ◽  
Primary Tumors ◽  
Hematogenous Dissemination ◽  
Node Metastases

Cancer cells metastasize from primary tumors to regional lymph nodes and distant sites via the lymphatic and blood vascular systems, respectively. Our prior work has demonstrated that in primary breast tumors, cancer cells utilize a three-cell complex (known as tumor microenvironment of metastasis, or TMEM) composed of a perivascular macrophage, a tumor cell expressing high levels of the actin-regulatory protein mammalian enabled (Mena), and an endothelial cell as functional “doorways” for hematogenous dissemination. Here, we studied a well-annotated case–control cohort of human invasive ductal carcinoma of the breast and metastatic lymph nodes from a separate breast cancer cohort. We demonstrate that in primary breast tumors, blood vessels are always present within tumor cell nests (TCNs) and tumor-associated stroma (TAS), while lymphatic vessels are only occasionally present in TCN and TAS. Furthermore, TMEM doorways not only exist in primary tumors as previously reported but also in lymph node metastases. In addition, we show that TMEM intravasation doorways are restricted to the blood vascular endothelium in both primary tumors and lymph node metastases, suggesting that breast cancer dissemination to distant sites from both primary tumors and metastatic foci in lymph nodes occurs hematogenously at TMEM doorways. TMEMs are very rarely detected at lymphatic vessels and do not confer clinical prognostic significance, indicating they are not participants in TMEM-associated hematogenous dissemination. These findings are consistent with recent observations that hematogenous dissemination from lymph nodes occurs via blood vessels.

scholarly journals Lymph-migrating, tissue-derived dendritic cells are minor constituents within steady-state lymph nodes

2008 ◽  
Vol 205 (12) ◽  
pp. 2839-2850 ◽  
Author(s):  
Claudia Jakubzick ◽  
Milena Bogunovic ◽  
Anthony J. Bonito ◽  
Emma L. Kuan ◽  
Miriam Merad ◽  
...  
Keyword(s):  
Dendritic Cells ◽  
Lymph Node ◽  
Steady State ◽  
Lymph Nodes ◽  
Lymphatic Vessels ◽  
Inflammatory Stimulus ◽  
Major Fraction ◽  
Reporter Mouse ◽  
Relationship Of ◽  
The Relationship

Observations that dendritic cells (DCs) constitutively enter afferent lymphatic vessels in many organs and that DCs in some tissues, such as the lung, turnover rapidly in the steady state have led to the concept that a major fraction of lymph node DCs are derived from migratory DCs that enter the lymph node through upstream afferent lymphatic vessels. We used the lysozyme M–Cre reporter mouse strain to assess the relationship of lymph node and nonlymphoid organ DCs. Our findings challenge the idea that a substantial proportion of lymph node DCs derive from the upstream tissue during homeostasis. Instead, our analysis suggests that nonlymphoid organ DCs comprise a major population of DCs within lymph nodes only after introduction of an inflammatory stimulus.

Rapid and Large-Scale Formation of Chondrocyte Aggregates by Rotational Culture

2003 ◽  
Vol 12 (5) ◽  
pp. 475-479 ◽  
Author(s):  
Katsuko S. Furukawa ◽  
Hideyuki Suenaga ◽  
Kenshi Toita ◽  
Akiko Numata ◽  
Junzo Tanaka ◽  
...  
Keyword(s):  
Culture System ◽  
Large Scale ◽  
Collagen Type ◽  
Articular Chondrocytes ◽  
Cell Interaction ◽  
Collagen Type I ◽  
Cell Contact ◽  
Type I ◽  
Pellet Culture ◽  
Cell Cell

Chondrocytes in articular cartilage synthesize collagen type II and large sulfated proteoglycans, whereas the same cells cultured in monolayer (2D) dedifferentiate into fibroblastic cells and express collagen type I and small proteoglycans. On the other hand, a pellet culture system was developed as a method for preventing the phenotypic modulation of chondrocytes and promoting the redifferentiation of dedifferentiated ones. Because the pellet culture system forms only one cell aggregate each tube by a centrifugator, the pellet could not be applied to produce a tissue-engineered cartilage. Therefore, we tried to form chondrocyte aggregates by a rotational culture, expecting to form a large number of aggregates at once. In order to increase cell–cell interactions and decrease chondrocyte–material interaction, dishes with low retention of protein adsorption and cell adhesiveness were used. In addition, rotational shaking of the dish including cells was attempted to increase the cell–cell interaction. The shaking speed was set at 80 rpm, so the cells would be distributed in the center of the dish to augment the frequency of cell–cell contact. Under these conditions, bovine articular chondrocytes started aggregating in a few hours. At 24–36 h of rotational culture, aggregates with smooth surfaces were observed. Parameters such as increase of culture time and addition of TGF-β controlled diameters of the aggregates. There were many fusiform cells at the periphery of the aggregates, where the cells tended to form a multilayered zone in cross sections. In addition, lacune-like structure, which was almost the same as pellet culture, was observed. It was found that the internal structure of the aggregates was similar to that of pellets reported previously. Therefore, the aggregates formed by a rotational culture could become an essential component to make tissue-engineered artificial cartilage.

scholarly journals Tumor cell entry into the lymph node is controlled by CCL1 chemokine expressed by lymph node lymphatic sinuses

2013 ◽  
Vol 210 (8) ◽  
pp. 1509-1528 ◽  
Author(s):  
Suvendu Das ◽  
Eliana Sarrou ◽  
Simona Podgrabinska ◽  
Melanie Cassella ◽  
Sathish Kumar Mungamuri ◽  
...  
Keyword(s):  
Cell Migration ◽  
Lymph Node ◽  
Lymph Nodes ◽  
Tumor Cell ◽  
Tumor Cells ◽  
Lymphatic Vessels ◽  
Cell Entry ◽  
Human Malignant Melanoma ◽  
Tumor Cell Migration ◽  
Mouse Tissues

Lymphatic vessels are thought to contribute to metastasis primarily by serving as a transportation system. It is widely believed that tumor cells enter lymph nodes passively by the flow of lymph. We demonstrate that lymph node lymphatic sinuses control tumor cell entry into the lymph node, which requires active tumor cell migration. In human and mouse tissues, CCL1 protein is detected in lymph node lymphatic sinuses but not in the peripheral lymphatics. CCR8, the receptor for CCL1, is strongly expressed by human malignant melanoma. Tumor cell migration to lymphatic endothelial cells (LECs) in vitro is inhibited by blocking CCR8 or CCL1, and recombinant CCL1 promotes migration of CCR8+ tumor cells. The proinflammatory mediators TNF, IL-1β, and LPS increase CCL1 production by LECs and tumor cell migration to LECs. In a mouse model, blocking CCR8 with the soluble antagonist or knockdown with shRNA significantly decreased lymph node metastasis. Notably, inhibition of CCR8 led to the arrest of tumor cells in the collecting lymphatic vessels at the junction with the lymph node subcapsular sinus. These data identify a novel function for CCL1–CCR8 in metastasis and lymph node LECs as a critical checkpoint for the entry of metastases into the lymph nodes.

scholarly journals Morphological and radiological study of lymph nodes in dromedaries in Algeria

2020 ◽  
Vol 11 (2) ◽  
pp. 330-337
Author(s):  
D. E. Rahmoun ◽  
M. A. Lieshchova ◽  
M. A. Fares
Keyword(s):  
Lymph Node ◽  
Lymph Nodes ◽  
General Structure ◽  
Lymphatic Vessels ◽  
Conventional Radiography ◽  
Farm Animals ◽  
Relative Mass ◽  
Linear Measurements ◽  
X Ray ◽  
The One

Despite significant progress in the study of the subtle mechanisms of interaction between cellular and molecular elements in immune responses, the general structure of the organs of the immune system, including the lymph node, has not been sufficiently studied, in particular in large farm animals. The lymph nodes of sexually mature camels have been studied anatomically and morphologically and advanced studies conducted using an X-ray system and a computer densitometer scanner with injection of a contrast medium. The topography and characteristics of the morphometric parameters (absolute and relative mass, linear measurements, volume) of certain somatic and visceral lymph nodes were determined. The mass of the lymph nodes studied varies according to the location and the interest of the organ in the satellite defense of the lymphoid system, For part of the x-ray examination of the lymph nodes, organs of large inguinal and axillary shape were selected after passing through a solution of tetraethyl-4,4-diamino-triphenylmethane oxalate, the lymph vessels were dilated and darkened, then iodine injections were made into the afferent lymphatic vessel of two lymph nodes; they were placed on the radiological cassette, a photograph taken on conventional radiography, for computer densitometer, the examination was made without preparation of the organs. A capsule encompasses the parenchyma of the lymph node, whose internal structure is composed of different zones, cortical, paracortical and medullary, on the one hand the lymphatic vessels were very clear especially with the conventional radiography with preparation of the organs, while the computer densitometer clearly revealed the deep texture of the parenchyma, basing it on the intensity of emission saturation from the use of computer densitometer.

scholarly journals Morphogenesis lymph node of domestic pig

2020 ◽  
pp. 102-109
Author(s):  
E. Gavrilina ◽  
A. Kolesnyk
Keyword(s):  
Lymph Node ◽  
Lymph Nodes ◽  
Lymphatic Vessels ◽  
Linear Measurements ◽  
Domestic Pig ◽  
Newborn Piglets ◽  
Connective Tissue Capsule ◽  
Degree Of Consolidation ◽  
Number Of Segments ◽  
Tissue Capsule

The visceral and somatic lymph nodes of a pig of domestic 1-120 day old were examined. Found that the lymph nodes have a common connective tissue capsule and different levels of fusion of individual subunits. In the center of each subunit, the capsule forms invaginations of the capsular trabecula, dividing the parenchyma of each structural unit into «Ʊ»-shaped structures, fused with lateral and lower parts. The number and degree of fusion of subunits is different and depends on the age of the animals and the location of the lymph node. The greatest degree of fusion of individual units of the lymph node was found in the superficial cervical and axillary I ribs. In the mandibular, superficial parotid and superficial inguinal lymph nodes, the segments are clearly contoured already in newborn piglets. Segments are predominantly bean-spherical in shape with a wide base. The fusion of the segments occurs in their central part, and on the surface the gates of the subunits are clearly contoured in the form of numerous depressions. In the visceral lymph nodes, the portal and splenic lymph nodes have the smallest segmentation, and the gastric, tracheobronchial, and iliocolic lymph nodes are the largest. The number of segments varies from two in newborn piglets to five in 120-day-old pigs. The variability of the morphometric parameters of the lymph nodes of a domestic pig is due to a different number of afferent lymphatic vessels, and, accordingly, to different scales of the lymphatic basins. Thus, the lymph nodes of the domestic pig are complexes of subunits fused to varying degrees. Somatic lymph nodes are highly segmented. The degree of consolidation of subunits in the visceral lymph nodes is less pronounced. Linear measurements of organs vary depending on the age of the animals, gradually increasing up to 120 days with a tendency for these indicators to prevail in the somatic lymph nodes. Key words: domestic pig, lymph node, subunit, topography, morphometry

scholarly journals Rgs1 and Gnai2 Regulate the Entrance of B Lymphocytes into Lymph Nodes and B Cell Motility within Lymph Node Follicles

Immunity ◽  
2005 ◽  
Vol 22 (3) ◽  
pp. 343-354 ◽  
Author(s):  
Sang-Bae Han ◽  
Chantal Moratz ◽  
Ning-Na Huang ◽  
Brian Kelsall ◽  
Hyeseon Cho ◽  
...  
Keyword(s):  
Lymph Node ◽  
Lymph Nodes ◽  
Cell Motility ◽  
B Cell ◽  
B Lymphocytes

scholarly journals HSV-1 Targets Lymphatic Vessels in the Eye and Draining Lymph Node of Mice Leading to Edema in the Absence of a Functional Type I Interferon Response

2013 ◽  
Vol 183 (4) ◽  
pp. 1233-1242 ◽  
Author(s):  
Katie M. Bryant-Hudson ◽  
Ana J. Chucair-Elliott ◽  
Christopher D. Conrady ◽  
Alex Cohen ◽  
Min Zheng ◽  
...  
Keyword(s):  
Lymph Node ◽  
Type I Interferon ◽  
Lymphatic Vessels ◽  
Interferon Response ◽  
Type I ◽  
Functional Type ◽  
Draining Lymph Node ◽  
Hsv 1

The Incidence and Clinical Significance of the Micrometastases in the Sentinel Lymph Nodes During Surgical Staging for Early Endometrial Cancer

2015 ◽  
Vol 25 (4) ◽  
pp. 673-680 ◽  
Author(s):  
Domenico Ferraioli ◽  
Nicolas Chopin ◽  
Frederic Beurrier ◽  
Nicolas Carrabin ◽  
Annie Buenerd ◽  
...  
Keyword(s):  
Endometrial Cancer ◽  
Lymph Node ◽  
Lymph Nodes ◽  
Clinical Significance ◽  
Prognostic Significance ◽  
Case Series ◽  
Lymph Node Status ◽  
Type I ◽  
Gynecology And Obstetrics ◽  
Histopathologic Features

IntroductionThe status of regional node remains one of the most important factors to guide adjuvant therapy in endometrial cancer (EC). Pelvic recurrence occurs in up to 15% of early EC patients with negative pelvic lymph nodes (LNs). The prognostic significance of detecting micrometastases (μM) in LN is debated. This retrospective case-control study performed in the Oncological Gynecology Department in Lyon between December 1998 and June 2012 reports the incidence and the clinical significance of μM detected during ultrastaging of negative sentinel lymph node (SLN) in EC.Patients and MethodsNinety-three patients affected by type I and II EC were submitted to surgery with SLN. Dual-labeling method was used to detect SLN. All the SLNs were subjected to ultrastaging researching μM. The patients with a locoregional or distant relapse represented the case-series (CS). The patients without locoregional or distant recurrences were the case-controls (CC).They were matched (1:2 ratio) according to age, International Federation of Gynecology and Obstetrics stage, and histopathologic features.ResultsTen patients presenting a relapse represented CS. In the remaining 83 patients without recurrence, 20 CC were individualized. The detection rate of SLN per hemipelvis was of 17 (85%) of 20 hemipelvis and of 33 (82.5%) of 40 hemipelvis for CS and CC, respectively. Two SLN of CS arm were positives at frozen section. One of the 8 patients of CS arm with negative SLNs was positive for μM by immunohistochemistry analysis.ConclusionsLymph node status is one of the most important histopathologic features to determine the adjuvant treatment. The SLN technique could be proposed in selected patients affected by early EC. The μM in SLN could be researched and could help to modulate the following treatment. The multicenter study must be performed to clarify the optimal method of research of SLN in EC and the significance of μM in the LN.

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