scholarly journals Immunohistological localization of alpha 1-microglobulin in normal rat tissues.

1984 ◽  
Vol 32 (7) ◽  
pp. 717-723 ◽  
Author(s):  
P Bouic ◽  
C Vincent ◽  
J P Revillard
Keyword(s):  
Dendritic Cells ◽  
Plasma Cells ◽  
Rabbit Antiserum ◽  
Secretory Component ◽  
Differential Staining ◽  
Secretory Cells ◽  
Lymphoid Tissues ◽  
White Pulp ◽  
Rat Tissues ◽  
Cytoplasmic Staining

The tissue distribution of rat alpha 1-microglobulin (alpha 1-m) was studied by indirect immunofluorescence in various rat tissues using a polyvalent rabbit antiserum to the purified antigen and a monoclonal antibody (H23) to the human homologue, in parallel with a polyclonal anti-rat IgA antiserum. It was found that all tissues stained by anti-IgA were also alpha 1-m positive; these tissues included tissues of the stomach, duodenum, ileum, colon, pancreas, trachea, esophagus and jejunum. However, the observation that IgA plasma cells as well as secretory cells, while positively stained by anti-IgA, are alpha 1-m negative suggests that the association between IgA and alpha 1-m occurs at a postsecretory stage, after the IgA molecules have been transported across the epithelial cells. Additionally, hepatocytes were intensely stained by anti-alpha 1-m antibodies, indicating that the liver, as already suggested by metabolic studies on isolated guinea-pig liver explants, may be responsible for the synthesis of this protein. Among lymphoid tissues, an intense and homogeneous staining was observed in the thymus and the white pulp of the spleen. Sections of lymph nodes, however, showed differential staining; apart from a few isolated dendritic cells in the mantle region of the lymphoid follicles, the germinal centers and medullary cords showed no staining with anti-alpha 1-m antibodies. The paracortical cells, macrophages in the subcapsular sinus, and interfollicular lymphocytes showed intense cytoplasmic staining with anti-alpha 1-m antibodies. In other tissues, macrophages, monocytes, tissue histiocytes, and dendritic cells were alpha 1-m positive. Although they confirm the presence of alpha 1-m in the lymphoid tissues, as already reported in man, these results show that the protein is also present in hepatocytes and in exocrine fluids containing IgA. Since alpha 1-m, like secretory component, can bind to IgA to form stable complexes, these two heavily glycosylated proteins may have similar biologic properties.

Architecture and Cellular Composition of the Spleen in the Japanese Quail (Coturnix japonica)

2020 ◽  
Vol 26 (3) ◽  
pp. 589-598 ◽  
Author(s):  
Fatma El-Zahraa A. Mustafa ◽  
Sara M.M. El-Desoky
Keyword(s):  
Blood Flow ◽  
Dendritic Cells ◽  
Japanese Quail ◽  
Blood Cells ◽  
Plasma Cells ◽  
Coturnix Japonica ◽  
White Pulp ◽  
Cellular Composition ◽  
Supporting Cells ◽  
Red Pulp

AbstractThe spleen is considered a key player in birds’ immunity. The stroma and the parenchyma of the spleen of the adult quail were demonstrated histologically, histochemically, and ultrastructurally. A thin capsule and the absence of trabeculae were the most characteristics of spleen stroma. The demarcation between white pulp and red pulp was not observed in the quail. White pulp formed from the periarterial lymphatic sheath and the periellipsoidal lymphatic sheath, both of which were surrounded by arteriole and ellipsoid, respectively. Ellipsoids appeared more numerous and were characterized by cuboidal lining of the epithelium and supporting cells. Red pulp consisted of sinuses and cords. White pulp and red pulp of the quail spleen contained various cells, such as red blood cells, macrophages, heterophils with characteristic granules, lymphocytes of different sizes, dendritic cells, plasma cells, and telocytes. In addition, closed circulation and open circulation established the blood flow on the spleen.

scholarly journals Monoclonal antibody 2H1 detects a 60-65 KD membrane polypeptide of the rough endoplasmic reticulum of neurons and selectively stains cells of several rat tissues.

1991 ◽  
Vol 39 (5) ◽  
pp. 635-643 ◽  
Author(s):  
Y J Chen ◽  
W F Hickey ◽  
S G Mezitis ◽  
A Stieber ◽  
E Lavi ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Endoplasmic Reticulum ◽  
Rough Endoplasmic Reticulum ◽  
Plasma Cells ◽  
Primary Cultures ◽  
White Pulp ◽  
Rat Tissues ◽  
Pc 12 Cells ◽  
Adrenal Medullary Cells ◽  
Medullary Cells

Monoclonal antibody (MAb) 2H1, raised in mice immunized with membrane fractions from cultured rat pheochromocytoma cells (clonal line PC-12), detects a polypeptide from rat brain and PC-12 cell membranes of 60-65 KD apparent molecular mass. The polypeptide has been localized by immunoelectron microscopy in the rough endoplasmic reticulum (RER) of neurons. By light microscopic immunocytochemistry, several rat tissues and two rat-derived cultured cell types show selective patterns of staining with 2H1. In the central nervous system, the antibody stains neuronal cytoplasm; in the spleen, staining is seen only in certain cells of the marginal zone of the white pulp, and in lymph nodes, in plasma cells, and in areas populated by monocytes and macrophages. Whereas astrocytes and adrenal medullary cells in situ are virtually unstained with 2H1, primary cultures of astrocytes and PC-12 cells, which are derived from adrenal medullary cells, stain intensely with 2H1. The strong staining of cultured astrocytes and PC-12 cells with 2H1 suggests that the levels of the 60-65 KD polypeptide are up-regulated during cell proliferation and growth. Only a few hepatocytes stain with 2H1; intestinal epithelial and pancreatic cells are not stained with 2H1. The organelle-specific antibody 2H1 may prove a useful probe in structural and functional studies of membranes of the rough endoplasmic reticulum in neurons, and in certain cells of the immune system.

scholarly journals Immunohistochemical localization of annexin V (CaBP33) in rat organs.

1991 ◽  
Vol 39 (9) ◽  
pp. 1189-1198 ◽  
Author(s):  
I Giambanco ◽  
G Pula ◽  
P Ceccarelli ◽  
R Bianchi ◽  
R Donato
Keyword(s):  
Skeletal Muscle ◽  
Endothelial Cells ◽  
Annexin V ◽  
Muscle Cells ◽  
Cell Types ◽  
Skeletal Muscle Cells ◽  
Secretory Cells ◽  
White Pulp ◽  
Rat Tissues ◽  
Peritubular Capillaries

We investigated the cellular distribution of annexin V (CaBP33) in rat tissues by immunohistochemistry. Several cell types were shown to express the protein. Glial cells in the cerebellum and in the optic nerve, the corneal epithelium, the posterior epithelium in the iris, chondrocytes, skeletal muscle cells and cardiomyocytes, the capillary endothelial cells in many organs, the muscularis mucosae and the muscular layer in the intestinal tract, hepatocytes, Müller cells in the retina, the lens fibers, Sertoli and Leydig cells in the testis, and smooth muscle cells in the epididymis and bronchi displayed intense immunostaining. In the adrenal gland, only the cortex showed immunoreaction product. In the kidney, no apparent staining of renal cells was observed, whereas endothelial cells of peritubular capillaries were stained. In the heart, annexin V was found associated exclusively with the sarcolemma and intercalated discs, as opposed to the diffuse distribution of the protein in skeletal muscle cells. In the spleen, only reticular elements in the white pulp and endothelial cells in the red pulp appeared to be immunostained. The present data complement the biochemical work thus far done on annexin V and suggest that the protein is neither restricted to secretory cells nor exclusively related to exocytotic events in secretory cells.

scholarly journals THE FUNCTIONS OF THE THYMUS SYSTEM AND THE BURSA SYSTEM IN THE CHICKEN

1966 ◽  
Vol 123 (1) ◽  
pp. 75-102 ◽  
Author(s):  
Max D. Cooper ◽  
Raymond D. A. Peterson ◽  
Mary Ann South ◽  
Robert A. Good
Keyword(s):  
Plasma Cells ◽  
Germinal Centers ◽  
Cell System ◽  
Delayed Hypersensitivity ◽  
Bursa Of Fabricius ◽  
Surgical Removal ◽  
Lymphoid Tissues ◽  
White Pulp ◽  
Dependent Development ◽  
Graft Versus Host

The bursa of Fabricius and the thymus are "central lymphoid organs" in the chicken, essential to the ontogenetic development of adaptive immunity in that species. Surgical removal of one or both of these organs in the newly hatched chicken, followed by sublethal X-irradiation the next day, has permitted recognition of two morphologically distinct cell systems in the "peripheral lymphoid tissues" of the spleen, gut, and other organs, and clear definition of the separate functions of each cell system. The thymus-dependent development is represented morphologically by the small lymphocytes of the circulation and the white pulp type of development in the tissues. As in mammals, the thymus-dependent tissues of the chicken are basic to the ontogenesis of cellular immunity: graft versus host reactions, responses of delayed hypersensitivity and homograft rejection; and play a less clearly defined role in the antibody response to at least some antigens. Thymectomized-irradiated chickens are deficient in all these responses, and grow more slowly than any of the other experimental groups. In these animals germinal centers, plasma cells, and capacity for immunoglobulin synthesis remain intact. The bursa-dependent development is represented morphologically by the larger lymphocytes of the germinal centers and the plasma cells, and functionally by the immunoglobulins. Bursectomized-irradiated chickens are agammaglobulinemic and unable to produce detectable antibody despite intense, repeated stimulation with bovine serum albumin and Brucella abortus organisms. The thymus-dependent development in these animals seems to be normal; they have adequate numbers of lymphocytes in the circulation and tissues, are able to reject skin homografts, though more slowly than usual, and to exercise graft versus host reactions. The short life span of these chickens has precluded adequate study of responses of delayed hypersensitivity. There was no evidence of significant impairment of reticuloendothelial function in either the bursectomized-irradiated or the thymectomized-irradiated group, as judged by the clearance of colloidal gold and I131-tagged keyhole limpet hemocyanin.

scholarly journals Histomorphological study of the lymphoid tissues of broiler chickens

1970 ◽  
Vol 4 (2) ◽  
pp. 87-92 ◽  
Author(s):  
S Akter ◽  
MZI Khan ◽  
MR Jahan ◽  
MR Karim ◽  
MR Islam
Keyword(s):  
Connective Tissue ◽  
Broiler Chickens ◽  
Plasma Cells ◽  
Splenic Tissue ◽  
Bursa Of Fabricius ◽  
Immunocompetent Cells ◽  
Lymphoid Tissues ◽  
White Pulp ◽  
Cecal Tonsil ◽  
Reticular Cells

Topology and histology were performed in the lymphoid tissues (thymus, bursa of Fabricius, spleen and cecal tonsils) of the fifteen 28-days-old "Kasilla" broilers by observation of H & E stained sections in the Department of Anatomy and Histology, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh during the period from October to December 2005. In the present study, it was observed that the thymus was enclosed by a thin connective tissue capsule. Numerous fine septa of connective tissue originated from the capsule and divide the organ into incompletely separated lobules. Each lobule organized into a peripheral cortex and a central medulla. The population of the immunocompetent cells (lymphocytes and immunoglobulin containing plasma cells) in the cortex were denser rather than that of medulla of the thymic lobule. The bursa of Fabricius was consisting of long thick mucosal folds (plicae). Numerous follicles filled the lamina propria of each fold and each bursal follicle was composed a peripheral cortex and a central medulla. The population of the immunocompetent cells in the cortex of the bursal follicle were denser rather than that of medulla of the bursal follicle. The spleen was surrounded by a thick splenic capsule and there was a small number of trabeculi. The network of the splenic tissue was consisting of a network of reticular cells and fibers and was arranged into red pulps, which were scatteredly distributed within the white pulps. The white pulp was composed of network of reticular cells and reticular fibers within which the immunocompetent cells were diffusely distributed. It contained sheathed arteries and lymphatic nodules. The red pulp of the spleen was formed from venous sinuses and anastomosing cord of reticular cells, macrophages, lymphocytes and blood cells. Cecal tonsil was composed of four histological layers i.e. tunica mucosa, submucosa, muscularis and serosa. Their lining epithelium was simple columnar epithelium. More diffuse lymphoid tissue and unorganized lymphatic nodules were present both in the mucosa and submucosa of the cecal tonsil of broiler. The length and breadth of the thymic lobules were 629.30 ± 118.95 µm and 376.03 ± 98.92 µm, bursal follicles 468.83 ± 52.26 µm and 240.70 ± 34.19 µm, white pulp of the spleen 112.62 ± 13.25 µm and 89.42 ± 12.20 µm, lymphatic nodules of the cecal tonsil 255.20 ± 20.46 µm and 186.08 ± 24.90 µm respectively. The result of the present study revealed that the immunocompetent cells were arranged scatteredly or densely and as unorganized or organized lymphatic nodules in the lymphoid tissues and the length and breadth of the thymic lobule, bursal follicle, splenic white pulp and lymphatic nodule of cecal tonsils were varied within the lymphoid tissues and even one another. Key words: Histology, lymphoid tissues, immunocompetent cells, broilersDOI = 10.3329/bjvm.v4i2.1289Bangl. J. Vet. Med. (2006). 4 (2): 87–92

scholarly journals HISTOMORPHOLOGICAL STUDY OF THE MAJOR LYMPHOID TISSUES IN INDIGENOUS DUCKLINGS OF BANGLADESH

2012 ◽  
Vol 9 (1) ◽  
pp. 53-58
Author(s):  
N Sultana ◽  
MZI Khan ◽  
MA Wares ◽  
MA Masum
Keyword(s):  
Connective Tissue ◽  
Plasma Cells ◽  
Immunocompetent Cells ◽  
Lymphoid Tissues ◽  
White Pulp ◽  
Drug Induced ◽  
Connective Tissue Capsule ◽  
Reticular Fibers ◽  
Reticular Cells ◽  
Mucosal Folds

A histomorphological study was performed in the major lymphoid tissues (thymus, bursa of Fabricus and spleen) of the six 21-day-old indigenous ducklings of Bangladesh by H & E staining method during the period from March to May 2011. In the present study, it was observed that the thymus was enclosed by a thin connective tissue capsule. Numerous fine septa of connective tissue originated from the capsule and divided the organ into incompletely separated lobules. Each lobule organized into a peripheral cortex and a central medulla. The bursa of Fabricus was consisted of mucosal folds (plicae). Numerous follicles filled the lamina propria of each fold and each bursal follicle was composed a peripheral cortex and a central medulla. A layer of undifferentiated epithelial cells occupied the periphery of the medulla, which was separated from the cortex by a capillary layer. The darkly stained cortex was composed of many closely packed small lymphocytes. The paler medulla contained fewer cells of various sizes. The spleen was surrounded by a thick splenic capsule and there were a small number of trabeculae. The white pulp was composed of network of reticular cells and reticular fibers within various size lymphocytes and plasma cells were diffusely distributed. The red pulp of the spleen was formed from venous sinuses and anastomosing cord of reticular cells, macrophages, lymphocytes and blood cells. The length and breadth of the thymic lobules, bursal follicles and white pulp of the spleen were 226.68 and 165.78cm, 204.45 and 138.23cm, and 129.05 and 103.43cm respectively. The result of the present work revealed that the immunocompetent cells were arranged scatteredly or densely as an unorganized lymphatic nodules in the lymphoid tissues. The length and breadth of the thymic lobules were higher followed by bursal follicle and splenic white pulps were varied within the lymphoid tissues and even one another in indigenous ducklings. The results of the present study indicate that the architecture and distribution of lymphocytes and lymphoid follicles of ducklings is very close to the chicken and this study might be helpful to understand the changes in the frequency of the population of immunocompetent cells in drug induced, vitamin and mineral supplemented or hormone treated duck in future.DOI = http://dx.doi.org/10.3329/bjvm.v9i1.11212 Bangl. J. Vet. Med. (2011). 9(1): 53-58 

Selective Generation of Gut-Tropic T Cells in Gut-Associated Lymphoid Tissues: Requirement for GALT Dendritic Cells and Adjuvant

2004 ◽  
Vol 1029 (1) ◽  
pp. 405-407 ◽  
Author(s):  
MARCUS SVENSSON ◽  
BENGT JOHANSSON-LINDBOM ◽  
MARC-ANDRÉ WURBEL ◽  
BERNARD MALISSEN ◽  
GABRIEL MÁRQUEZ ◽  
...  
Keyword(s):  
T Cells ◽  
Dendritic Cells ◽  
Lymphoid Tissues ◽  
Selective Generation

KLRL1, a novel killer cell lectinlike receptor, inhibits natural killer cell cytotoxicity

Blood ◽  
2004 ◽  
Vol 104 (9) ◽  
pp. 2858-2866 ◽  
Author(s):  
Yanmei Han ◽  
Minghui Zhang ◽  
Nan Li ◽  
Taoyong Chen ◽  
Yi Zhang ◽  
...  
Keyword(s):  
Dendritic Cells ◽  
Natural Killer ◽  
Nk Cell ◽  
Killer Cell ◽  
Cell Receptor ◽  
Sh2 Domain ◽  
Target Cells ◽  
Lymphoid Tissues ◽  
Nk Cell Receptor ◽  
Human And Mouse

Abstract Natural killer (NK) cell inhibitory receptors play important roles in the regulation of target susceptibility to natural killing. Here, we report the molecular cloning and functional characterization of a novel NK cell receptor, KLRL1, from human and mouse dendritic cells. KLRL1 is a type II transmembrane protein with an immunoreceptor tyrosine-based inhibitory motif and a C-type lectinlike domain. The KLRL1 gene is located in the central region of the NK gene complex in both humans and mice, on human chromosome 12p13 and mouse chromosome 6F3, adjacent to the other KLR genes. KLRL1 is preferentially expressed in lymphoid tissues and immune cells, including NK cells, T cells, dendritic cells, and monocytes or macrophages. Western blot and fluorescence confocal microscopy analyses indicated that KLRL1 is a membrane-associated glycoprotein, which forms a heterodimer with an as yet unidentified partner. Human and mouse KLRL1 are both predicted to contain putative immunoreceptor tyrosine-based inhibitory motifs (ITIMs), and immunoprecipitation experiments demonstrated that KLRL1 associates with the tyrosine phosphatases SHP-1 (SH2-domain-containing protein tyrosine phosphatase 1) and SHP-2. Consistent with its potential inhibitory function, pretreatment of target cells with human KLRL1-Fc fusion protein enhances NK-mediated cytotoxicity. Taken together, our results demonstrate that KLRL1 belongs to the KLR family and is a novel inhibitory NK cell receptor.

scholarly journals Accessory and stimulating properties of dendritic cells and macrophages isolated from various rat tissues

1982 ◽  
Vol 156 (1) ◽  
pp. 1-19 ◽  
Author(s):  
WEF Klinkert ◽  
JH LaBadie ◽  
WE Bowers
Keyword(s):  
T Cells ◽  
Dendritic Cells ◽  
Cell Activity ◽  
Accessory Cell ◽  
Nonspecific Esterase ◽  
Rat Tissues ◽  
Low Density ◽  
Γ Irradiation ◽  
Accessory Cells ◽  
Ia Antigens

Single cell suspensions of rat lymphoid and nonlymphoid tissues were fractionated on discontinuous gradients of bovine serum albumin into high density and low density subfractions. In general, accessory activity required for responses of periodate-treated T lymphocytes was recovered only in a low density population containing a small percent of the total fractionated cells from lymph nodes, spleen, liver, skin, and peritoneal exudates. Further purification always led to an increase of both accessory activity and number of dendritic cells present in nonrosetting and nonadherent populations. After purification, a high recovery of the total accessory activity was found in fractions that contained a high percentage of dendritic cells resulting in a more than 1,000-fold enrichment in accessory activity per cell. No other fraction obtained during the purification contained significant accessory activity. In all cases, macrophage-enriched populations lacked accessory cell activity. With the exception of peritoneal exudate cell preparations, which contained an inhibitory cell, the level of accessory activity in a given population was always found to be a function of the number of dendritic cells present. Dendritic cells from all sources were nonadherent, nonphagocytic, radio- resistant, and nonspecific esterase negative. They expressed Ia antigens and lacked Fc receptors. Both epidermal and lymph node dendritic cells contain Birbeck granules, subcellular structures previously described only for Langerhans cells. Accessory activity requires viable dendritic cells but is unaffected by 1,000 rad of γ-irradiation. However, ultraviolet irradiation abolished the activity of accessory cells. The cells that responded to periodate were IgG-negative T cells, whereas IgG-positive B cells could not be stimulated under the same conditions. Only periodate-treated T cells and dendritic cells were needed for responses to occur; removal of virtually all macrophages from these purified preparations had no effect. Dendritic cells were also required as stimulators in mixed leukocyte cultures, whereas macrophages, even though Ia positive, were inert.

scholarly journals Establishment and characterization of a human plasma cell myeloma culture having a rearranged cellular myc proto-oncogene

Blood ◽  
1986 ◽  
Vol 67 (6) ◽  
pp. 1542-1549 ◽  
Author(s):  
AF Gazdar ◽  
HK Oie ◽  
IR Kirsch ◽  
GF Hollis
Keyword(s):  
Cell Line ◽  
Human Plasma ◽  
Plasma Cell ◽  
Plasma Cells ◽  
Cultured Cells ◽  
Human Cell Line ◽  
Defined Medium ◽  
Chromosome 8 ◽  
Nuclear Antigen ◽  
Secretory Cells

Using a serum-free defined medium, we have established a human cell line, NCI-H929, from a malignant effusion occurring in a patient with IgAk myeloma. The cultured cells have the morphologic, ultrastructural, biochemical, immunologic, and cytochemical features of plasma cells. The cells have rearranged alpha and kappa genes and synthesize and secrete high amounts of IgAk (greater than 80 micrograms/10(6) cells per 24 hours). The cells express surface immunoglobulin (alpha and kappa), the plasma cell antigen PCA-1, the transferrin receptor (T9) and T10 but lack antigens associated with earlier stages of B cell development (HLA-DR, B1, B2, B4, CALLA), as well as other leukocyte- macrophage antigens and Epstein-Barr virus (EBV) nuclear antigen. Although molecular studies confirm that both the tumor and cultured cells are derived from the same clone of malignant B cells, the tumor cells were predominantly near-diploid, whereas the cultured cells are predominantly near-tetraploid with six copies of chromosome 8, four to six of which have an 8q + abnormality. However, both the tumor and the cultured cells have a rearrangement of the cellular c-myc proto- oncogene (located at 8q24) and express c-myc RNA. Although a modest number of human “plasmacytoid” cell lines have been established, most are lymphoblastoid lines lacking plasma cell features, while others appear to be early secretory cells. In contrast, NCI-H929 is a differentiated, highly secretory human plasma cell line.

Sign in / Sign up

Export Citation Format

Share Document