Embryonic origins of spleen asymmetry

Development ◽  
2000 ◽  
Vol 127 (1) ◽  
pp. 167-175 ◽  
Author(s):  
K.D. Patterson ◽  
T.A. Drysdale ◽  
P.A. Krieg
Keyword(s):  
Molecular Markers ◽  
Homeobox Gene ◽  
Subsequent Development ◽  
Splenic Tissue ◽  
Precursor Cells ◽  
The Body ◽  
Body Axis ◽  
Cellular Mechanisms ◽  
Immunologic Function ◽  
Organ Specific

The spleen is a vertebrate organ that has both hematopoietic and immunologic function. The embryonic origins of the spleen are obscure, with most studies describing the earliest rudiment of the spleen as a condensation of mesodermal mesenchyme on the left side of the dorsal mesogastrium. The development of spleen handedness has not been described previously, presumably because of the difficulty in assaying spleen position in the embryo and the lack of early, organ-specific molecular markers. Here we show that expression of the homeobox gene Nkx2-5 serves as a marker for spleen precursor tissue. Pre-splenic tissue is initially located in symmetric domains on both sides of the embryo but, during subsequent development, only the left side goes on to form the mature spleen. Therefore, the final location of the spleen on the left side of the body axis appears to result from preferential development of the spleen precursor cells on the left side of the embryo. Our studies indicate that the spleen and heart become asymmetric via different cellular mechanisms. Nkx2-5 may function locally as part of the laterality cascade, downstream of nodal and Pitx2, or it may direct asymmetric morphogenesis after laterality has been determined.

End Organ Toxicities of Adverse Drug Reactions

1989 ◽  
Vol 2 (4) ◽  
pp. 245-250
Author(s):  
Theresa A. Salazar
Keyword(s):  
Bone Marrow ◽  
Adverse Drug Reaction ◽  
Adverse Effects ◽  
Subsequent Development ◽  
Organ System ◽  
The Body ◽  
Drug Reactions ◽  
Diagnostic Problem ◽  
Drug Induced ◽  
Organ Specific

Many commonly prescribed medications are capable of causing organ specific adverse effects that can involve every organ system of the body. This situation presents the clinician with a diagnostic problem, since the drug-induced illness often mimics the clinical - disease. Clinicians must be alert to the possibility that drugs can cause or exacerbate any disease. In order to assess effectively the possibility of an illness being a result of an adverse drug reaction, it is necessary to recognize the manifestations of that drug's adverse effects and indict the drug on the basis of its use and the subsequent development of illness. This article reviews the organ-specific toxicities of drugs known to affect the liver, kidney, blood and bone marrow, and ear.

Expression of Cnox-2, a HOM/HOX homeobox gene in hydra, is correlated with axial pattern formation

Development ◽  
1993 ◽  
Vol 117 (2) ◽  
pp. 657-667 ◽  
Author(s):  
M.A. Shenk ◽  
H.R. Bode ◽  
R.E. Steele
Keyword(s):  
Pattern Formation ◽  
Epithelial Cells ◽  
Homeobox Gene ◽  
Specific Pattern ◽  
The Body ◽  
Body Axis ◽  
Hydra Vulgaris ◽  
Coordinate Reduction ◽  
High Level ◽  
Body Column

Cnox-2 is a HOM/HOX homeobox gene that we have identified in the simple metazoan Hydra vulgaris (Cnidaria: Hydrozoa). Cnox-2 is most closely related to anterior members of the Antennapedia gene complex from Drosophila, with the greatest similarity to Deformed. The Cnox-2 protein is expressed in the epithelial cells of adult hydra polyps in a region-specific pattern along the body axis, at a low level in the head and at a high level in the body column and the foot. The expression pattern of Cnox-2 is consistent with a role in axial pattern formation. Alteration of hydra axial patterning by treatment with diacylglycerol (DAG) results in an increase of head activation down the body column and in a coordinate reduction of Cnox-2 expression in epithelial cells in ‘head-like’ regions. These results suggest that Cnox-2 expression is negatively regulated by a signaling pathway acting through protein kinase C (PKC), and that the varying levels of expression of Cnox-2 along the body axis have the potential to result in differential gene expression which is important for hydra pattern formation.

scholarly journals Inflammation-Related Carcinogenesis: Lessons from Animal Models to Clinical Aspects

Cancers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 921
Author(s):  
Futoshi Okada ◽  
Runa Izutsu ◽  
Keisuke Goto ◽  
Mitsuhiko Osaki
Keyword(s):  
Animal Models ◽  
Tissue Injury ◽  
Economic Status ◽  
Gene Mutations ◽  
Inflammatory Cells ◽  
The Body ◽  
Clinical Aspects ◽  
Promote Cell Proliferation ◽  
Organ Specific ◽  
Altered Gene

Inflammation-related carcinogenesis has long been known as one of the carcinogenesis patterns in humans. Common carcinogenic factors are inflammation caused by infection with pathogens or the uptake of foreign substances from the environment into the body. Inflammation-related carcinogenesis as a cause for cancer-related death worldwide accounts for approximately 20%, and the incidence varies widely by continent, country, and even region of the country and can be affected by economic status or development. Many novel approaches are currently available concerning the development of animal models to elucidate inflammation-related carcinogenesis. By learning from the oldest to the latest animal models for each organ, we sought to uncover the essential common causes of inflammation-related carcinogenesis. This review confirmed that a common etiology of organ-specific animal models that mimic human inflammation-related carcinogenesis is prolonged exudation of inflammatory cells. Genotoxicity or epigenetic modifications by inflammatory cells resulted in gene mutations or altered gene expression, respectively. Inflammatory cytokines/growth factors released from inflammatory cells promote cell proliferation and repair tissue injury, and inflammation serves as a “carcinogenic niche”, because these fundamental biological events are common to all types of carcinogenesis, not just inflammation-related carcinogenesis. Since clinical strategies are needed to prevent carcinogenesis, we propose the therapeutic apheresis of inflammatory cells as a means of eliminating fundamental cause of inflammation-related carcinogenesis.

scholarly journals Development of a new method for assessing otolith function in mice using three-dimensional binocular analysis of the otolith-ocular reflex

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shotaro Harada ◽  
Takao Imai ◽  
Yasumitsu Takimoto ◽  
Yumi Ohta ◽  
Takashi Sato ◽  
...  
Keyword(s):  
Eye Movement ◽  
Three Dimensional ◽  
Vertical Component ◽  
Inertial Force ◽  
Linear Acceleration ◽  
The Body ◽  
Body Axis ◽  
Gravitational Acceleration ◽  
Ocular Reflex ◽  
Translational Movement

AbstractIn the interaural direction, translational linear acceleration is loaded during lateral translational movement and gravitational acceleration is loaded during lateral tilting movement. These two types of acceleration induce eye movements via two kinds of otolith-ocular reflexes to compensate for movement and maintain clear vision: horizontal eye movement during translational movement, and torsional eye movement (torsion) during tilting movement. Although the two types of acceleration cannot be discriminated, the two otolith-ocular reflexes can distinguish them effectively. In the current study, we tested whether lateral-eyed mice exhibit both of these otolith-ocular reflexes. In addition, we propose a new index for assessing the otolith-ocular reflex in mice. During lateral translational movement, mice did not show appropriate horizontal eye movement, but exhibited unnecessary vertical torsion-like eye movement that compensated for the angle between the body axis and gravito-inertial acceleration (GIA; i.e., the sum of gravity and inertial force due to movement) by interpreting GIA as gravity. Using the new index (amplitude of vertical component of eye movement)/(angle between body axis and GIA), the mouse otolith-ocular reflex can be assessed without determining whether the otolith-ocular reflex is induced during translational movement or during tilting movement.

scholarly journals The thymus and the science of self

2021 ◽  
Author(s):  
Vincent Geenen
Keyword(s):  
T Cells ◽  
Adaptive Immune System ◽  
Lymphoid Organ ◽  
The Body ◽  
Effector Cells ◽  
Major Organ ◽  
Organ Specific ◽  
Health And Disease ◽  
Essential State ◽  
The 1960S

AbstractThe conventional perception asserts that immunology is the science of ‘discrimination’ between self and non-self. This concept is however no longer tenable as effector cells of the adaptive immune system are first conditioned to be tolerant to the body’s own antigens, collectively known as self until now. Only then attain these effectors the responsiveness to non-self. The acquisition of this essential state of tolerance to self occurs for T cells in the thymus, the last major organ of our body that revealed its intricate function in health and disease. The ‘thymus’ as an anatomical notion was first notably documented in Ancient Greece although our present understanding of the organ’s functions was only deciphered commencing in the 1960s. In the late 1980s, the thymus was identified as the site where clones of cells reactive to self, termed ‘forbidden’ thymocytes, are physically depleted as the result of a process now known as negative selection. The recognition of this mechanism further contributed to the belief that the central rationale of immunology as a science lies in the distinction between self and non-self. This review will discuss the evidence that the thymus serves as a unique lymphoid organ able to instruct T cells to recognize and be tolerant to harmless self before adopting the capacity to defend the body against potentially injurious non-self-antigens presented in the context of different challenges from infections to exposure to malignant cells. The emerging insight into the thymus’ cardinal functions now also provides an opportunity to exploit this knowledge to develop novel strategies that specifically prevent or even treat organ-specific autoimmune diseases.

The Caenorhabditis elegans gene lin-44 controls the polarity of asymmetric cell divisions

Development ◽  
1994 ◽  
Vol 120 (5) ◽  
pp. 1035-1047 ◽  
Author(s):  
M.A. Herman ◽  
H.R. Horvitz
Keyword(s):  
Caenorhabditis Elegans ◽  
The Body ◽  
Body Axis ◽  
Nematode Caenorhabditis Elegans ◽  
Asymmetric Cell Divisions ◽  
Cell Divisions ◽  
Sister Cells

The generation and orientation of cellular and organismic polarity are fundamental aspects of development. Mutations in the gene lin-44 of the nematode Caenorhabditis elegans reverse both the relative positions of specific sister cells and the apparent polarities of these cells. Thus, lin-44 mutants appear to generate polar cells but to misorient these cells along the body axis of the animal. We postulate that lin-44 acts to specify the orientation of polar cells.

Mechanism of anteroposterior axis specification in vertebrates. Lessons from the amphibians

Development ◽  
1992 ◽  
Vol 114 (2) ◽  
pp. 285-302 ◽  
Author(s):  
J.M. Slack ◽  
D. Tannahill
Keyword(s):  
Molecular Markers ◽  
Expression Patterns ◽  
Signal Transduction Pathway ◽  
Homeobox Gene ◽  
Neural Induction ◽  
High Sensitivity ◽  
Neural Plate ◽  
Mesoderm Induction ◽  
Inducing Factors ◽  
Almost All

Interest in the problem of anteroposterior specification has quickened because of our near understanding of the mechanism in Drosophila and because of the homology of Antennapedia-like homeobox gene expression patterns in Drosophila and vertebrates. But vertebrates differ from Drosophila because of morphogenetic movements and interactions between tissue layers, both intimately associated with anteroposterior specification. The purpose of this article is to review classical findings and to enquire how far these have been confirmed, refuted or extended by modern work. The “pre-molecular” work suggests that there are several steps to the process: (i) Formation of anteroposterior pattern in mesoderm during gastrulation with posterior dominance. (ii) Regional specific induction of ectoderm to form neural plate. (iii) Reciprocal interactions from neural plate to mesoderm. (iv) Interactions within neural plate with posterior dominance. Unfortunately, almost all the observable markers are in the CNS rather than in the mesoderm where the initial specification is thought to occur. This has meant that the specification of the mesoderm has been assayed indirectly by transplantation methods such as the Einsteckung. New molecular markers now supplement morphological ones but they are still mainly in the CNS and not the mesoderm. A particular interest attaches to the genes of the Antp-like HOX clusters since these may not only be markers but actual coding factors for anteroposterior levels. We have a new understanding of mesoderm induction based on the discovery of activins and fibroblast growth factors (FGFs) as candidate inducing factors. These factors have later consequences for anteroposterior pattern with activin tending to induce anterior, and FGF posterior structures. Recent work on neural induction has implicated cAMP and protein kinase C (PKC) as elements of the signal transduction pathway and has provided new evidence for the importance of tangential neural induction. The regional specificity of neural induction has been reinvestigated using molecular markers and provides conclusions rather similar to the classical work. Defects in the axial pattern may be produced by retinoic acid but it remains unclear whether its effects are truly coordinate ones or are concentrated in certain regions of high sensitivity. In general the molecular studies have supported and reinforced the “pre-molecular ones”. Important questions still remain: (i) How much pattern is there in the mesoderm (how many states?) (ii) How is this pattern generated by the invaginating organizer? (iii) Is there one-to-one transmission of codings to the neural plate? (iv) What is the nature of the interactions within the neural plate? (v) Are the HOX cluster genes really the anteroposterior codings?

Head positioning control in a gravito-inertial field and in normal gravity

2004 ◽  
Vol 14 (4) ◽  
pp. 321-333
Author(s):  
Frédéric Sarès ◽  
Christophe Bourdin ◽  
Jean-Michel Prieur ◽  
Jean-Louis Vercher ◽  
Jean-Pierre Menu ◽  
...  
Keyword(s):  
Inertial Force ◽  
The Body ◽  
Body Axis ◽  
Positioning Control ◽  
Head Positioning ◽  
Subject Variability ◽  
Visual Frame ◽  
Vector Orientation ◽  
The Right ◽  
Within Subject Variability

The way in which the head is controlled in roll was investigated by dissociating the body axis and the gravito-inertial force orientation. Seated subjects (N = 8) were requested to align their head with their trunk, 30° to the left, 30° to the right or with the gravito-inertial vector, before, during (Per Rotation), after off-center rotation and on a tilted chair without rotation (Tilted). The gravito-inertial vector angle during rotation and the chair tilt angle were identical (17°). The subjects were either in total darkness or facing a visual frame that was fixed to the trunk. Both final error and within-subject variability of head positioning increased when the body axis and the gravito-inertial vector were dissociated (Per Rotation and Tilted). However, the behavior was different depending on whether the subjects were in the Tilted or Per Rotation conditions. The presentation of the visual frame reduced the within-subject variability and modified the perception of the gravito-inertial vector's orientation on the tilted chair. As head positioning with respect to the body and sensing of the gravito-inertial vector are modified when body axis and gravito-inertial vector orientation are dissociated, the observed decrease in performance while executing motor tasks in a gravito-inertial field may be at least in part attributed to the inaccurate sensing of head position.

scholarly journals The body water compartments in women with preeclampsia in the peripartum period

2021 ◽  
Vol 17 (7) ◽  
pp. 20-23
Author(s):  
O.M. Klygunenko ◽  
O.О. Marzan
Keyword(s):  
Pregnant Women ◽  
Extracellular Fluid ◽  
Subsequent Development ◽  
Bioelectrical Impedance ◽  
Body Water ◽  
Fluid Volume ◽  
The Body ◽  
Severe Preeclampsia ◽  
Water Compartments ◽  
Total Fluid

Background. Preeclampsia in pregnant women is a threatening condition that causes significant water imbalance, particularly hyperhydration of the extracellular fluid compartment. The condition is the result of the main pathogenetic processes — endothelial dysfunction and the subsequent development of hypoproteinemia. The changes can be detected by measuring body water compartments. Objective: to investigate the effect of a standard intensive care on the body water compartment indicators in women with moderate to severe preeclampsia. Materials and methods. Ninety patients divided into three groups were examined: non-pregnant healthy women, pregnant women with healthy pregnancy, and women whose pregnancy was complicated by moderate to severe preeclampsia. Body water compartments were measured by non-invasive bioelectrical impedance analysis. Results. Pregnancy complicated by preeclampsia is accompanied by an increase in total fluid volume at 34–40 weeks due to an increase in both the extracellular and intracellular water compartments, but with a predominance of the extracellular compartment. By the 7th day of the postpartum period, there is a tendency to decrease the total fluid volume, however, interstitial and intracellular edema can be still observed. Conclusions. The results of the bioelectrical impe-dance analysis of the body water compartments show that additional methods of treatment are needed to correct the body water compartments in women with preeclampsia.

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