scholarly journals Histomorphological study of the spleen in indigenous Gazelle (Gazella subgutturosa)

2018 ◽  
Vol 41 (2) ◽  
pp. 100-105
Author(s):  
S. M. Mirhish
Keyword(s):  
Connective Tissue ◽  
Research Work ◽  
White Pulp ◽  
X Rays ◽  
Cellular Element ◽  
Splenic Parenchyma ◽  
Resin Injection ◽  
Adjacent Structures ◽  
Injection Methods ◽  
Red Pulp

     The study aimed to investigate the anatomical and histomorphometrical features of spleen in gazelle. To achieve this goal, spleens of 7 animals were used. The gross aspect of the study revealed that the spleen of gazelle appeared dark brown in color with elliptical shape and was situated at the left lateral surface of the rumen. It occupied the area extended from the 8th rib to 11th rib. Length and width of the spleens were calculated and the mean were 7.94±0.1, 5.88±0.2 respectively. There were three ligaments connected the spleen with adjacent structures, namely splenogastric, splenorenal and splenophrenic. The blood supply of the spleen was studied using X-rays and resin injection methods. The splenic artery was divided into three primary branches, each one subdivided into two secondary branches. The latter branched into tertiary branches which were distributed all over the splenic parenchyma. Microscopic findings showed that the capsule of spleen in gazelle was composed from of two layers, the outer one made of mainly of dense connective tissue; whereas the inner layer of capsule consisted of connective tissue fibers in addition to abundance of smooth muscle fibers interweaving among them. The total mean thickness of the capsule was 210.51+8.3 µm. The splenic parenchyma in gazelle consisted of white pulp represented by lymphoid follicles with their marginal zones and periarterial lymphatic sheath while the red pulp represented by splenic cords and sinusoids. The area of white pulp in the gazelle comprised about 9.6% of the spleen parenchyma. Red pulp composed mainly from cords of connective tissue and small sinuses or sinusoids filled with blood cellular element which extended among these cords and was lined by flattened endothelial cells with relatively large spaces or slits between them. The sinusoids were found to be lymphocytes, reticular, plasma, macrophages and occasional megakaryocytes whereas the megakaryocyte appeared large with acidophilic cytoplasm and dark elongated multilobated nucleus. This research work was performed in order to establish the basic histomorphological information helpful for the veterinary medical practice and veterinary surgions to developing their work on gazelle like designing the approach of some surgical operations like spleenectomy or any surgical entrance may be needed in these animal species.

scholarly journals Ascorbic acid biosynthesis: a precursor study on plants

2004 ◽  
Vol 16 (3) ◽  
pp. 147-154 ◽  
Author(s):  
Anderson D. Barata-Soares ◽  
Maria Luiza P. A. Gomez ◽  
Carlos Henrique de Mesquita ◽  
Franco M. Lajolo
Keyword(s):  
Ascorbic Acid ◽  
Sweet Pepper ◽  
The Other ◽  
White Pulp ◽  
Acid Biosynthesis ◽  
Ripe Fruit ◽  
Ripening Stages ◽  
Main Pathway ◽  
Ascorbic Acid Biosynthesis ◽  
Red Pulp

Since the first isolation of ascorbic acid (AsA) in 1928, few papers have been published regarding the biosynthesis of AsA in plants, especially in fruits. It took as long as 1998, before Wheeler, Jones and Smirnoff, based on a study with Arabidopsis leaves, proposed what can be considered the main pathway of biosynthesis of AsA, in which L-galactose (L-GAL) is a key precursor. This paper reports the effectiveness of some precursors (cold or radiolabeled) in the biosynthesis of AsA in different plants: green sweet pepper, white-pulp guava, red-pulp guava, papaya and strawberry at two ripening stages (mature green and ripe for papaya and mature green and half red for strawberry) and broccoli. The 'Smirnoff-Wheeler' pathway was functioning and active in all sources studied, as demonstrated by the increase in AsA contents and incorporation of labeled precursors into AsA. In papaya, the AsA content in the ripe fruit was higher than in the mature green, indicating the synthesis of AsA during ripening. On the other hand, the AsA content in the mature green strawberry was similar to that of the half red fruits. Our data demonstrate that L-GAL and L-Galactono-1,4-lactone (L-GL) are effective precursors for the biosynthesis of AsA in fruits and also provided additional evidence for the participation of D-mannose (D-MAN) and D-glucose-1P in the biosynthesis of AsA in plants.

scholarly journals Splenic Mechanisms of Thrombocytopenia

Blood ◽  
2017 ◽  
Vol 130 (Suppl_1) ◽  
pp. SCI-33-SCI-33
Author(s):  
John W. Semple
Keyword(s):  
Immune Responses ◽  
Reticuloendothelial System ◽  
Lymphoid Organ ◽  
The Body ◽  
White Pulp ◽  
Cellular Mechanisms ◽  
Venous Circulation ◽  
Destructive Processes ◽  
Clinical Conditions ◽  
Red Pulp

The spleen is the largest secondary lymphoid organ in the body and contains up to 25 percent of the body's lymphocyte populations. It is not only responsible for initiating immune responses against a multitude of infectious antigens within its white pulp, it also has the exquisite ability to filter the blood and remove, for example, senescent erythrocytes and platelets. This natural process is carried out within the red pulp of the spleen which is composed monocyte-rich connective tissue cords of Billroth intertwined with sinus cavities lined by parallel-oriented endothelial cells that have interendothelial slits which allow for the mechanical sorting of "old" cells. This occurs because of the inability of the senescent cells to properly migrate through the endothelial fenestrae into the venous circulation allowing them to be identified by cells of the reticuloendothelial system (RES) and quickly destroyed by phagocytosis. This process also allows for the efficient recycling of iron from destroyed erythrocyte hemoglobin molecules. There are a wide variety of clinical conditions that can significantly alter the ability of the RES to destroy blood cells including hereditary blood cell defects, inflammation, cancer and abnormal immune responses. This lecture will focus on the central role that the spleen plays in not only generating immune responses against platelets but also in primarily causing the destruction of both senescent and antibody-opsonized platelets leading to thrombocytopenia. It will discuss the soluble and cellular mechanisms of splenic sequestration, destruction and the ability of the spleen to modulate anti-platelet immunity. Mechanisms involving complement activation, Fc Receptor-mediated phagocytosis, antibody dependent cellular cytotoxicity and platelet self-destruction will be addressed. It will compare the spleen's platelet destructive capabilities with other organs, particularly the liver and will detail how immune responses generated in the white pulp can modulate platelet destructive processes in the red pulp. Disclosures Semple: Amgen: Consultancy, Honoraria, Speakers Bureau; Rigel: Consultancy, Honoraria; UCB: Consultancy, Honoraria.

Internal Structural Connections in the Popliteal Muscle Tendon Complex and Their Clinical Significance

2021 ◽  
Author(s):  
WenBin Jiang ◽  
Shi-Zhu Sun ◽  
Ting-Wei Song ◽  
Chan Li ◽  
Wei Tang ◽  
...  
Keyword(s):  
Connective Tissue ◽  
Knee Joint ◽  
Tibial Plateau ◽  
Lateral Meniscus ◽  
Posterior Edge ◽  
Dense Connective Tissue ◽  
Human Knee ◽  
Articular Capsule ◽  
Adjacent Structures ◽  
Popliteus Muscle

Abstract Background:The popliteal muscle-tendon complex (PMTC) belongs to the deep structure of the posterolateral complex (PLC) of human knee, which plays an important role in the posterolateral stability of the knee joint. At present, the anatomical relationship between the popliteal muscle and its adjacent structures remains controversial, especially the posterior cruciate ligament (PCL) and popliteal muscle. The revealation of anatomical connection between the popliteus muscle and its deep structures could provide an anatomical basis for the reconstruction of the PLC injury.Methods: To observe and analyze the relationship between popliteal muscle and the PCL, posterior meniscofemoral ligament (PMFL), lateral meniscus and articular capsule (AC). The dissection of 7 cases of adult human knee joint fixed with formalin, and 9 cases of sagittal P45 plastinated section of the knee joint were involved in this study. Results: For the popliteal muscle, the anatomical dissection showed that at the posterior edge of the platform of the lateral condyle of the tibia, at the tendon-muscle transition, from medial to lateral, separately sent out: dense connective tissue to connect with the PCL, dense fiber bundles to connect with the PMFL, and dense connective tissue band to connect the lateral meniscus. Meanwhile, the results of the P45 section revealed that the popliteal muscle fascia ran superiorly over the posterior edge of the tibialintercondylar eminence, andturned forward to be integrated into the PCL. Laterally, near the posterior edge of the lateral tibial plateau, the popliteal tendon penetrates through the articular capsule, where two dense fiberous bundleswere given off upwards by the popliteal tendon: one was the ventral fiber bundle,which ran superiorly over the posterior edge of the tibial plateau and then moved forwards to connect with the lateral meniscus; the dorsal fibersbundle ascended directly and participated in the AC.Conclusion: Popliteus muscle was connected with PCL, AC, lateral meniscus, and PMFL via the dense connective tissues near its tendon-muscle transition.

scholarly journals MicroRNA in localized scleroderma: a review of literature

2019 ◽  
Vol 312 (5) ◽  
pp. 317-324 ◽  
Author(s):  
Katarzyna Wolska-Gawron ◽  
Joanna Bartosińska ◽  
Dorota Krasowska
Keyword(s):  
Extracellular Matrix ◽  
Connective Tissue ◽  
Noncoding Rna ◽  
Extracellular Matrix Proteins ◽  
Tissue Growth ◽  
Matrix Proteins ◽  
Mitogen Activated Protein Kinase ◽  
Localized Scleroderma ◽  
Mesenchymal Transition ◽  
Adjacent Structures

Abstract Localized scleroderma (LoSc) is rare connective tissue disease that manifests with inflammation and fibrosis of the skin. Depending on the LoSc subtype, adjacent structures such as subcutaneous tissue, fascia, muscles, bones may be affected. The hallmark of fibrosis is tissue remodelling with excess deposition of extracellular matrix proteins (ECM), principally collagens. MicroRNAs (miRNAs) are small, noncoding RNA molecules that consist of 19–24 nucleotides and act as negative regulators of gene expression at the posttranscriptional level. Based on the current articles, approximately 40 microRNAs have been linked to fibrosis in different organs and diseases. The majority of these molecules promote or inhibit fibrosis by targeting connective tissue growth factor (CTGF), extracellular matrix proteins, TGF-β pathway and MAPK (mitogen-activated protein kinase) pathway. Further, particular microRNAs regulate fibrogenesis by altering epithelial-to-mesenchymal transition (EMT) or activating proliferation of myofibroblasts. MiRNAs are relatively stable, detectable in tissues and body fluids (serum, plasma) which suggest that they may serve as beneficial biomarkers to monitor the course of the disease and response to treatment. Herein, we report the present state of knowledge on microRNA expression in localized scleroderma.

scholarly journals Long-term follow-up of patients with anti-cyclic citrullinated peptide antibody-positive connective tissue disease: a retrospective observational study including information on the HLA-DRB1 allele and citrullination dependency

2020 ◽  
Vol 22 (1) ◽  
Author(s):  
Takeshi Iwasaki ◽  
Shuichiro Nakabo ◽  
Chikashi Terao ◽  
Kosaku Murakami ◽  
Ran Nakashima ◽  
...  
Keyword(s):  
Connective Tissue ◽  
Connective Tissue Disease ◽  
X Rays ◽  
Bone Erosions ◽  
Cyclic Citrullinated Peptide ◽  
Drb1 Allele ◽  
Antibody Titers ◽  
Hands And Feet ◽  
Citrullinated Peptide

Abstract Background The anti-cyclic citrullinated peptide (CCP) antibody is a diagnostic biomarker of rheumatoid arthritis (RA). However, some non-RA connective tissue disease (CTD) patients also test positive for the anti-CCP antibody and, thus, may ultimately develop RA. We retrospectively investigated whether anti-CCP-positive non-RA CTD patients developed RA and attempted to identify factors that may differentiate RA-overlapping CTD from pure CTD. Methods In total, 842 CTD patients with a primary diagnosis that was not RA were selected from our CTD database as of December 2012. Anti-CCP antibody titers were obtained from a retrospective chart review or measured using stored sera. RA was diagnosed according to the 1987 revised American College of Rheumatology classification criteria. Thirty-three anti-CCP-positive non-RA CTD patients were retrospectively followed up for the development of RA. Bone erosions on the hands and feet were assessed by X-ray. Citrullination dependency was evaluated by an in-house ELISA, the HLA-DRB1 allele was typed, and the results obtained were then compared between RA-overlapping and non-RA anti-CCP-positive CTD patients. Results Two out of 33 anti-CCP-positive CTD patients (6.1%) developed RA during a mean follow-up period of 8.9 years. X-rays were examined in 27 out of the 33 patients, and only one (3.7%) showed bone erosions. The frequency of the HLA-DRB1 shared epitope (SE) and anti-CCP antibody titers were both significantly higher in anti-CCP-positive RA-overlapping CTD patients than in anti-CCP-positive non-RA CTD patients, while no significant differences were observed in citrullination dependency. Conclusions Anti-CCP-positive non-RA CTD patients rarely developed RA. HLA-DRB1 SE and anti-CCP antibody titers may facilitate the differentiation of RA-overlapping CTD from anti-CCP-positive non-RA CTD.

Splenomegaly and other disorders of the spleen

2018 ◽  
Author(s):  
Chris Bunch
Keyword(s):  
Particulate Matter ◽  
Immune Responses ◽  
Lymphoid Tissue ◽  
Lymphoid Organ ◽  
Dual Role ◽  
White Pulp ◽  
Humoral Immune ◽  
Humoral Immune Responses ◽  
Upper Abdomen ◽  
Red Pulp

The spleen is a predominantly lymphoid organ, normally about the size of a clenched fist located beneath the diaphragm in the left upper abdomen. It has a dual role as a filter for the circulation, and a primary lymphoid organ in its own right. About three-quarters of its volume is a matrix of capillaries and sinuses (the red pulp), through which blood is able to percolate slowly and come into contact with fixed macrophages, which are able to remove senescent or damaged red cells, or other particulate matter such as bacteria. The lymphoid tissue is organized into scattered follicles (the white pulp), which have a particularly important role in initiating primary humoral immune responses and antibody (IgM) synthesis. The spleen commonly enlarges when either its filtration function is increased—as in haemolysis—or it is stimulated by infection or inflammation. It may also be involved in myeloproliferative and lymphoproliferative neoplasias. This chapter covers hypersplenism, splenectomy, hyposplenism, overwhelming post-splenectomy infection (OPSI), and other infections in hyposplenic patients.

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 Association of Immunofluorescence pattern of Antinuclear Antibody with Specific Autoantibodies in the Bangladeshi Population

2015 ◽  
Vol 40 (2) ◽  
pp. 74-78 ◽  
Author(s):  
S Sharmin ◽  
S Ahmed ◽  
A Abu Saleh ◽  
F Rahman ◽  
MR Choudhury ◽  
...  
Keyword(s):  
Connective Tissue ◽  
Lupus Erythematosus ◽  
Antinuclear Antibody ◽  
Research Work ◽  
Connective Tissue Disorder ◽  
Nuclear Antigen ◽  
Dot Blot ◽  
Serum Samples ◽  
Speckled Pattern ◽  
Extractable Nuclear Antigen

Antinuclear antibody (ANA) is useful in the diagnosis of connective tissue disorder (CTD). Association of specific autoantibodies with the immunofluorescence pattern of ANA in CTD, noted in western literature has been considered as reference in all over the world. However, in Bangladesh no such research work or data correlating the autoantibodies and their ANA patterns is found. Objective of the study was to identify an association between immunofluorescence patterns of antinuclear antibody on HEp-2 cell and more specific antinuclear reactivities (e.g. anti-dsDNA and anti-extractable nuclear antigen) in the serum samples of CTD patients. Serum samples of 152 CTD patients (Systemic lupus erythematosus, Rhumatoid arthritis, Sjogren´s syndrome, Systemic sclerosis, Polymyositis, Mixed connective tissue disease) were diagnosed clinically, attending at Bangabandhu Sheikh Mujib Medical University (BSMMU) during the study period of January, 2010 to December, 2010. Samples were subjected for ANA testing by Indirect Immunofluorescence (IIF) on HEp-2 cell (ALPHADIA) in dilution of 1:40, anti-dsDNA by ELISA and anti- extractable nuclear antigen (anti-ENA) by Dot Immunoblot. Dot blot strips were tested for anti-Sm, anti-RNP, anti-SSA/Ro, anti-SSB/La, anti-Scl-70 and anti-Jo-1. Out of 152 patients 110 (72.3%) cases were ANA positive by IIF on HEp-2 cell. ANA positive sera exhibited four fluorescence patterns such as speckled (50.8%), peripheral (21.6%) ,homogenous (18.1%) and nucleolar pattern (9%). Peripheral pattern and homogenous pattern was predominantly associated with anti-dsDNA (p<0.05). Speckled pattern was significantly associated with anti-ENA (p<0.05).The most commonly identified antinuclear autoreactivity was directed towards anti-RNP (25.7%) then anti-Scl-70 (20%), anti-SSA (14.2%) and anti-SSB (5.7%). Multiple anti-ENA reactivities were identified in 34.28% cases. Peripheral and homogenous pattern is strongly associated with anti-dsDNA and speckled pattern may predict anti-ENA (specially ribonucleoprotiens). As a definite correlation between the ANA patterns and the group of antibodies was detected by dot immunoblot, one could predict presence of certain specific auto antibodies for a particular ANA pattern identified. This may restrict on the cost of laboratory investigations in a developing country like Bangladesh. Thus, ANA-IIF method may reduce the expense of detailed immunological work-up with minimal loss in diagnostic accuracy.Bangladesh Med Res Counc Bull 2014; 40 (2): 74-78

REACTION OF THE LYMPHOID SPLENIC TISSUE IN WHITE MICE ON AMYLOIDOGENESIS

2020 ◽  
pp. 30-36
Author(s):  
Liliya Yu. Ilyina ◽  
Vadim A. Kozlov ◽  
Sergey P. Sapozhnikov ◽  
Ruslan A. Geraev
Keyword(s):  
Splenic Tissue ◽  
Case Group ◽  
White Pulp ◽  
Paraffin Sections ◽  
Morphological Pattern ◽  
Experimental Amyloidosis ◽  
Field Of Vision ◽  
Hematoxylin And Eosin ◽  
The Mean ◽  
Red Pulp

The reaction of lymphoid splenic tissue of mice on albumin model of systemic amyloidosis (case group, N = 5) was studied and compared to a similar indicator of intact mice (N = 5). Paraffin sections of the spleen, stained with hematoxylin and eosin and Congo red, were microscoped in a regredient LED white light on "Lumam-4" microscope. The absolute area of lymphatic follicles (LFs), their diameters and the area of amyloid lesion were measured on microphotos obtained with the help of video-eyepiece Levenhuk C800 NG 8M in LevenhukLite program. The obtained data were used for calculating the indicators: the relative areas of amyloid lesion (SrelA)), the red (SrelKB) and the white (SrelBP) pulp, the red/white pulp index, LFs' ovalityindex. The number of LFs was counted in the field of vision at magnification of 100. The obtained data were processed using the methods of descriptive and variative statistics and presented in the form of M±m, where M is the mean, m is the standard deviation. Differences of the means were determined using z test. The morphological pattern of the spleen in intact mice corresponded to the histological norm. The wet mass of the spleen in intact animals was 0.75±0.01 g, no signs of amyloidosis were found. In the case group, the wet mass of the spleen increased to 2.2±0.06 g (p=0.000), SrelA was 33.85± 3.39%. The average number of LFs in the field of vision did not change. The diameters by the large and small axes differed by 18% in intact animals and by 6.6% in experimental ones (p=0.000). Respectively, the area of LFs decreased by 11.2% and the ovality index increased by 10.3% (p = 0.0066) in experimental mice. SrelKB and SrelBPdid not change during the formation of amyloidosis. But the Red/White Pulp Index increased by 59.2% (p=0.008). Simulation of amyloidosis in experimental animals was accompanied by a significant increase in the area of the red pulp and by a reduction in the area of white pulp. Thus, the calculated relative morphometric indicators are more informative than the directly measured initial data; the wet mass of the spleen during experimental amyloidosis formation significantly increases; the lymphoid tissue of the spleen readily responds to amyloidogenesis by the change in the ratio of the red and white pulp, as well as by the change in the shape and the area of the lymph follicles.

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