scholarly journals Histology and Cell Biology: An Introduction to Pathology 5th Edition 2020

Morphologia ◽  
2021 ◽  
Vol 15 (1) ◽  
pp. 92-98
Author(s):  
Abraham L Kierszenbaum M.D. Ph.D., Laura Tres M.D. Ph.D.
Keyword(s):  
Concept Mapping ◽  
Cell Biology ◽  
Cell Receptor ◽  
Microtubule Assembly ◽  
Human Spleen ◽  
Fully Integrated ◽  
Award Winning ◽  
Green Background ◽  
Gestational Trophoblastic Diseases ◽  
Beginning Learners

Linking basic science to clinical application throughout, Histology and Cell Biology: An Introduction to Pathology, 5th Edition, helps students build a stronger clinical knowledge base in the challenging area of pathologic abnormalities. This award-winning text presents key concepts in an understandable, easy-to-understand manner, with full-color illustrations, diagrams, photomicrographs, and pathology photos fully integrated on every page. Student-friendly features such as highlighted clinical terms, Clinical Conditions boxes, Essential Concepts boxes, concept mapping animations, and more help readers quickly grasp complex information. Features new content on cancer immunotherapy, satellite cells and muscle repair, vasculogenesis and angiogenesis in relation to cancer treatment, and mitochondria replacement therapies. Presents new material on ciliogenesis, microtubule assembly and disassembly, chromatin structure and condensation, and X chromosome inactivation, which directly impact therapy for ciliopathies, infertility, cancer, and Alzheimer’s disease. Provides thoroughly updated information on gestational trophoblastic diseases, molecular aspects of breast cancer, and basic immunology, including new illustrations on the structure of the T-cell receptor, CD4+ cells subtypes and functions, and the structure of the human spleen. Uses a new, light green background throughout the text to identify essential concepts of histology – a feature requested by both students and instructors to quickly locate which concepts are most important for beginning learners or when time is limited. These essential concepts are followed by more detailed information on cell biology and pathology. Contains new Primers in most chapters that provide a practical, self-contained integration of histology, cell biology, and pathology – perfect for clarifying the relationship between basic and clinical sciences. Identifies clinical terms throughout the text and lists all clinical boxes in the table of contents for quick reference. Helps students understand the links between chapter concepts with concept mapping animations on Student Consult™ – an outstanding supplement to in-class instruction. Student Consult™ eBook version included with purchase. This enhanced eBook experience allows you to search all of the text, figures, and references from the book on a variety of devices.

Cell Biology of T Cell Receptor Expression and Regulation

2018 ◽  
Vol 36 (1) ◽  
pp. 103-125 ◽  
Author(s):  
Andrés Alcover ◽  
Balbino Alarcón ◽  
Vincenzo Di Bartolo
Keyword(s):  
T Cell ◽  
T Cell Receptor ◽  
Cell Biology ◽  
Cell Receptor ◽  
Receptor Expression

scholarly journals T Cell Receptor Specificity Is Critical for the Development of Epidermal γδ T Cells

2001 ◽  
Vol 194 (10) ◽  
pp. 1473-1483 ◽  
Author(s):  
Isabel Ferrero ◽  
Anne Wilson ◽  
Friedrich Beermann ◽  
Werner Held ◽  
H. Robson MacDonald
Keyword(s):  
T Cells ◽  
T Cell ◽  
T Cell Receptor ◽  
Cell Biology ◽  
Γδ T Cells ◽  
Cell Receptor ◽  
Wild Type ◽  
Normal Numbers ◽  
T Cell Biology

A particular feature of γδ T cell biology is that cells expressing T cell receptor (TCR) using specific Vγ/Vδ segments are localized in distinct epithelial sites, e.g., in mouse epidermis nearly all γδ T cells express Vγ3/Vδ1. These cells, referred to as dendritic epidermal T cells (DETC) originate from fetal Vγ3+ thymocytes. The role of γδ TCR specificity in DETC's migration/localization to the skin has remained controversial. To address this issue we have generated transgenic (Tg) mice expressing a TCR δ chain (Vδ6.3-Dδ1-Dδ2-Jδ1-Cδ), which can pair with Vγ3 in fetal thymocytes but is not normally expressed by DETC. In wild-type (wt) Vδ6.3Tg mice DETC were present and virtually all of them express Vδ6.3. However, DETC were absent in TCR-δ−/− Vδ6.3Tg mice, despite the fact that Vδ6.3Tg γδ T cells were present in normal numbers in other lymphoid and nonlymphoid tissues. In wt Vδ6.3Tg mice, a high proportion of in-frame Vδ1 transcripts were found in DETC, suggesting that the expression of an endogenous TCR-δ (most probably Vδ1) was required for the development of Vδ6.3+ epidermal γδ T cells. Collectively our data demonstrate that TCR specificity is essential for the development of γδ T cells in the epidermis. Moreover, they show that the TCR-δ locus is not allelically excluded.

scholarly journals Deciphering the Immunological Phenomenon of Adaptive Natural Killer (NK) Cells and Cytomegalovirus (CMV)

2020 ◽  
Vol 21 (22) ◽  
pp. 8864
Author(s):  
Samantha Barnes ◽  
Ophelia Schilizzi ◽  
Katherine M. Audsley ◽  
Hannah V. Newnes ◽  
Bree Foley
Keyword(s):  
Nk Cells ◽  
Natural Killer ◽  
Cell Biology ◽  
Nk Cell ◽  
Cell Receptor ◽  
Vital Role ◽  
Immune Memory ◽  
Target Cells ◽  
Cytokines And Chemokines ◽  
Adaptive Immune Cells

Natural killer (NK) cells play a significant and vital role in the first line of defense against infection through their ability to target cells without prior sensitization. They also contribute significantly to the activation and recruitment of both innate and adaptive immune cells through the production of a range of cytokines and chemokines. In the context of cytomegalovirus (CMV) infection, NK cells and CMV have co-evolved side by side to employ several mechanisms to evade one another. However, during this co-evolution the discovery of a subset of long-lived NK cells with enhanced effector potential, increased antibody-dependent responses and the potential to mediate immune memory has revolutionized the field of NK cell biology. The ability of a virus to imprint on the NK cell receptor repertoire resulting in the expansion of diverse, highly functional NK cells to this day remains a significant immunological phenomenon that only occurs in the context of CMV. Here we review our current understanding of the development of these NK cells, commonly referred to as adaptive NK cells and their current role in transplantation, infection, vaccination and cancer immunotherapy to decipher the complex role of CMV in dictating NK cell functional fate.

scholarly journals RNA-Seq analysis of early transcriptional responses to activation in the leukaemic Jurkat E6.1 T cell line

2020 ◽  
Vol 5 ◽  
pp. 42 ◽  
Author(s):  
Suet Ling Felce ◽  
Gillian Farnie ◽  
Michael L. Dustin ◽  
James H. Felce
Keyword(s):  
T Cell ◽  
Cell Line ◽  
Cell Biology ◽  
Cell Receptor ◽  
Rna Seq ◽  
Sequencing Data ◽  
Transcriptional Responses ◽  
Human T Cells ◽  
T Cell Biology ◽  
Whole Transcriptome

Background: The leukaemia-derived Jurkat E6.1 cell line has been used as a model T cell in the study of many aspects of T cell biology, most notably activation in response to T cell receptor (TCR) engagement. Methods: We present whole-transcriptome RNA-Sequencing data for Jurkat E6.1 cells in the resting state and two hours post-activation via TCR and CD28. We compare early transcriptional responses in the presence and absence of the chemokines CXCL12 and CCL19, and perform a basic comparison between observed transcriptional responses in Jurkat E6.1 cells and those in primary human T cells using publicly deposited data. Results: Jurkat E6.1 cells have many of the hallmarks of standard T cell transcriptional responses to activation, but lack most of the depth of responses in primary cells. Conclusions: These data indicate that Jurkat E6.1 cells hence represent only a highly simplified model of early T cell transcriptional responses.

scholarly journals Self-recognition drives the preferential accumulation of promiscuous CD4+ T-cells in aged mice

eLife ◽  
2015 ◽  
Vol 4 ◽  
Author(s):  
Neha R Deshpande ◽  
Heather L Parrish ◽  
Michael S Kuhns
Keyword(s):  
T Cells ◽  
T Cell ◽  
Cd4 T Cells ◽  
Cell Biology ◽  
Fold Increase ◽  
Cell Receptor ◽  
Cd4 T Cell ◽  
Fundamental Aspect ◽  
Cell Compartment ◽  
Old Mice

T-cell recognition of self and foreign peptide antigens presented in major histocompatibility complex molecules (pMHC) is essential for life-long immunity. How the ability of the CD4+ T-cell compartment to bind self- and foreign-pMHC changes over the lifespan remains a fundamental aspect of T-cell biology that is largely unexplored. We report that, while old mice (18–22 months) contain fewer CD4+ T-cells compared with adults (8–12 weeks), those that remain have a higher intrinsic affinity for self-pMHC, as measured by CD5 expression. Old mice also have more cells that bind individual or multiple distinct foreign-pMHCs, and the fold increase in pMHC-binding populations is directly related to their CD5 levels. These data demonstrate that the CD4+ T-cell compartment preferentially accumulates promiscuous constituents with age as a consequence of higher affinity T-cell receptor interactions with self-pMHC.

scholarly journals Understanding SARS CoV-2 biology to win COVID-19 battle

2020 ◽  
Vol 23 (2) ◽  
Author(s):  
Cristiane Yumi Koga-Ito ◽  
Henrique Toshiaki Koga-Ito ◽  
Aline Da Graça Sampaio ◽  
Mariana Raquel da Cruz Vegian
Keyword(s):  
Cell Biology ◽  
Standard Treatment ◽  
Cell Receptor ◽  
Host Cells ◽  
World Health ◽  
Angiotensin Converting Enzyme 2 ◽  
Novel Variant ◽  
Therapeutic Protocols ◽  
Health Organization ◽  
No Gold Standard

This review highlights the main findings on the biology of SARS CoV-2 and the strategies to combat COVID 19 pandemic. Since the initial outbreak in China on December 2019, the international scientific community joined efforts in an unprecedent public health battle. In late May 2020, 5 204 508 cases and 337 687 deaths have been reported by World Health Organization, with higher number of cases in Europe and Americas. SARS-CoV-2 was described as a novel variant from the coronavirus family and its genome was sequenced within a few months while COVID 19 quickly spread worldwide. The main cell receptor (angiotensin converting enzyme 2) was identified as involved in the invasion of host cells. As a result of the findings from cell biology, immunology and clinical studies, the pathogenesis of the virus started to be understood but it has been not fully elucidated so far. While a massive effort for the development of a vaccine is on course, preventive protocols for infection control have been proposed. Many studies on the discovering of effective therapeutic protocols have been developed, particularly on the redirection of already approved substances, but no gold standard treatment was established until now. An overview on the envisioned socioeconomic and politic impacts suggest that our society will be transformed after COVID 19 pandemia. As a result, deep changes in science, politics, socioeconomic and healthcare priorities shall appear in post-pandemia agenda.KEYWORDSCovid-19; Pandemic; SARS-CoV-2; Coronavirus. Key-words: COVID 19, pandemia, SARS-CoV-2, coronavirus.

scholarly journals Phospholipase Cγ1 is essential for T cell development, activation, and tolerance

2010 ◽  
Vol 207 (2) ◽  
pp. 309-318 ◽  
Author(s):  
Guoping Fu ◽  
Yuhong Chen ◽  
Mei Yu ◽  
Andy Podd ◽  
James Schuman ◽  
...  
Keyword(s):  
T Cells ◽  
T Cell ◽  
Cell Biology ◽  
T Cell Development ◽  
Cell Receptor ◽  
Cell Development ◽  
Phospholipase Cγ1 ◽  
T Cell Biology ◽  
Single Positive ◽  
And Function

Phospholipase Cγ1 (PLCγ1) is an important signaling effector of T cell receptor (TCR). To investigate the role of PLCγ1 in T cell biology, we generated and examined mice with T cell–specific deletion of PLCγ1. We demonstrate that PLCγ1 deficiency affects positive and negative selection, significantly reduces single-positive thymocytes and peripheral T cells, and impairs TCR-induced proliferation and cytokine production, and the activation of ERK, JNK, AP-1, NFAT, and NF-κB. Importantly, PLCγ1 deficiency impairs the development and function of FoxP3+ regulatory T cells, causing inflammatory/autoimmune symptoms. Therefore, PLCγ1 is essential for T cell development, activation, and tolerance.

From Literary Orphans to Award-winning Authorship: Serbian Migrant Writers in Australia

2017 ◽  
Vol 13 (1) ◽  
pp. 36-55
Author(s):  
Nataša Kampmark
Keyword(s):  
New Wave ◽  
World War ◽  
Fully Integrated ◽  
Two Cultures ◽  
Literary Community ◽  
Privileged Position ◽  
Award Winning ◽  
The World ◽  
Migrant Writing

Focusing on literary careers of individual writers, this paper traces the trajectory of Serbian migrant writing in Australia from its beginnings after World War ii until the present, arguing that this writing has progressively evolved from being part of a doubly neglected ghetto-like literary community to becoming a fully integrated, award-winning authorship. Each new wave of migrants is viewed as a link in the chain of evolution triggered by migration understood as a change of place. In the case of migrant writers and writers of non-Anglo-Celtic background in Australia, the advantages gained by migration include the access to a large bilingual cultural pool, a doubly informed vision and interpretation of the world, and the privileged position of a mediator between two cultures.

The growth of cutaneous T-cell lymphoma is stimulated by immature dendritic cells

Blood ◽  
2002 ◽  
Vol 99 (8) ◽  
pp. 2929-2939 ◽  
Author(s):  
Carole L. Berger ◽  
Douglas Hanlon ◽  
Daniel Kanada ◽  
Madhav Dhodapkar ◽  
Vivian Lombillo ◽  
...  
Keyword(s):  
T Cell ◽  
Cell Biology ◽  
Cell Lymphoma ◽  
Close Association ◽  
Clinical Intervention ◽  
Cell Receptor ◽  
T Cell Lymphoma ◽  
Cutaneous T Cell Lymphoma

Abstract In the initial stage of cutaneous T-cell lymphoma (CTCL), proliferating CTCL cells are concentrated in the epidermis in close association with an immature dendritic cell (DC), the Langerhans cell. Because long-term in vitro culture of CTCL cells has proven difficult, the in vivo association with the major antigen-presenting cell (APC) of the epidermis has been postulated to play a role in directly stimulating the clonal T-cell proliferation. We report that CTCL cells can be reproducibly grown in culture for 3 months when cocultured with immature DCs. CTCL cells retain the phenotype and genotype of the initial malignant clone, whereas the APCs are a mixture of immature and mature DCs. CTCL cell and DC survival was dependent on direct membrane contact. Growth was inhibited by antibodies that bound to the T-cell receptor (TCR) or interfered with the interaction of CD40 with its ligand on the CTCL cell. Addition of antibody to CD3 or the clonotypic TCR caused rapid CTCL cell apoptosis followed by engulfment by avidly phagocytic immature DCs and subsequent DC maturation. The opportunity to study CTCL cells and immature DCs for prolonged periods will facilitate studies of tumor cell biology and will allow investigation of the intriguing hypothesis that CTCL cell growth is driven through TCR recognition of class II–presented self-peptides. In addition, the culture of CTCL cells will permit evaluation of therapies in vitro before clinical intervention, thereby improving safety and efficacy.

The cell biology of T-dependent B cell activation

1989 ◽  
Vol 67 (9) ◽  
pp. 481-489 ◽  
Author(s):  
Trevor Owens ◽  
Rana Zeine
Keyword(s):  
T Cells ◽  
T Cell ◽  
B Cell ◽  
T Cell Receptor ◽  
Cell Biology ◽  
Cell Activation ◽  
Cell Receptor ◽  
Cellular Interaction ◽  
B Cell Activation ◽  
Intercellular Interaction

The requirement that CD4+ helper T cells recognize antigen in association with class II Major Histocompatibility Complex (MHC) encoded molecules constrains T cells to activation through intercellular interaction. The cell biology of the interactions between CD4+ T cells and antigen-presenting cells includes multipoint intermolecular interactions that probably involve aggregation of both polymorphic and monomorphic T cell surface molecules. Such aggregations have been shown in vitro to markedly enhance and, in some cases, induce T cell activation. The production of T-derived lymphokines that have been implicated in B cell activation is dependent on ligation of the T cell receptor for antigen and its associated CD3 signalling complex. T-dependent help for B cell activation is therefore similarly MHC-restricted and involves T–B intercellular interaction. Recent reports that describe antigen-independent B cell activation through coculture with T cells activated by anti-T-cell receptor or anti-CD3 antibodies suggest that cellular interaction with T cells, independent of antigen presentation or lymphokine secretion, induces or triggers B cells to become responsive to T-derived lymphokines, and that this may be an integral component of the physiological, antigen- and MHC-restricted T-dependent B cell activation that leads to antibody production.Key words: T helper, B cell, activation, contact, lymphokines.

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