1.

Record Nr.

UNISA996465256203316

Autore

Thuswald Marion

Titolo

Sexuelle Bildung ermöglichen : Sprachlosigkeit, Lust, Verletzbarkeit und Emanzipation als Herausforderungen pädagogischer Professionalisierung / / Marion Thuswald

Pubbl/distr/stampa

Bielefeld : , : transcript Verlag, , [2022]

©2022

Descrizione fisica

1 online resource (502 p.)

Collana

Pädagogik

Classificazione

DG 5000

Soggetti

EDUCATION / Philosophy, Theory & Social Aspects

Lingua di pubblicazione

Tedesco

Formato

Materiale a stampa

Livello bibliografico

Monografia

Nota di contenuto

Frontmatter -- Inhaltsverzeichnis -- Einleitung -- TEIL I. Sexualpädagogik in der Pädagog*innenbildung beforschen: Gesellschaftliche, theoretische und methodische Rahmungen -- Einleitung -- 1. Sexualität als pädagogisches Thema -- 2. Sexualpädagogische Professionalisierung -- 3. Ethnografie als Forschungsstrategie -- TEIL II. Theoretisierende Beschreibungen: Zu den didaktischen Praktiken sexualpädagogischer Aus- und Fortbildungen -- Einleitung -- 4. Sexualpädagogische Bildungsveranstaltungen eröffnen -- 5. Praxisorientierte Lernsettings gestalten -- 6. Professionelle Ansprüche und didaktische Spielräume ausloten -- TEIL III. Machtkritische Analysen: Zwischen Lustfreundlichkeit, Differenzreflexivität und Gewaltprävention vermitteln -- Einleitung -- 7. Zum Verständnis von Sexualität: Lebensenergie, Ausdruck von Liebe oder erotische Praxis? -- 8. Sexuelle Vielfalt thematisieren: Heteronormativität herausfordern? -- 9. Sexuelle Übergriffe zum Thema machen: (K)eine Sprache anbieten? -- 10. Möglichkeitsräume sexueller Bildung ausloten: Pädagogische Herausforderungen reflektieren -- AUSBLICK. Sexualpädagogische Fragen als Schlüsselproblem pädagogischer Professionalisierung -- Literatur- und Quellenverzeichnis -- Sachregister -- Personen- und Organisationenregister -- Danke

Sommario/riassunto

Wie werden Lehrer*innen auf sexualpädagogische Herausforderungen



in der Schule vorbereitet? Und welcher Stellenwert kommt dabei Lustfreundlichkeit, sexueller Vielfalt, Gewaltprävention und Antidiskriminierung zu? In ihrer soziografischen Studie untersucht Marion Thuswald sexualpädagogische Aus- und Fortbildungsveranstaltungen von Pädagogischen Hochschulen, Fachstellen und Universitäten in Österreich. Anhand einer kritischen Analyse sexualpädagogischer Praktiken lotet sie Möglichkeitsräume emanzipatorisch orientierter sexueller Bildung aus und entwickelt praxisnahe Optimierungsvorschläge für Schulen und Lehrer*innenbildung.

2.

Record Nr.

UNINA9910220050103321

Titolo

Dendritic Cell and Macrophage Nomenclature and Classification

Pubbl/distr/stampa

Frontiers Media SA, 2016

Descrizione fisica

1 online resource (202 p.)

Collana

Frontiers Research Topics

Disciplina

616.07/9

Soggetti

Medicine

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Sommario/riassunto

The mononuclear phagocyte system (MPS) comprises dendritic cells (DCs), monocytes and macrophages (MØs) that together play crucial roles in tissue immunity and homeostasis, but also contribute to a broad spectrum of pathologies. They are thus attractive therapeutic targets for immune therapy. However, the distinction between DCs, monocytes and MØ subpopulations has been a matter of controversy and the current nomenclature has been a confounding factor. DCs are remarkably heterogeneous and consist of multiple subsets traditionally defined by their expression of various surface markers. While markers are important to define various populations of the MPS, they do not specifically define the intrinsic nature of a cell population and do not always segregate a bona fide cell type of relative homogeneity. Markers



are redundant, or simply define distinct activation states within one subset rather than independent subpopulations. One example are the steady-state CD11b+ DCs which are often not distinguished from monocytes, monocyte-derived cells, and macrophages due to their overlapping phenotype. Lastly, monocyte fate during inflammation results in cells bearing the phenotypic and functional features of both DCs and MØs significantly adding to the confusion. In fact, depending on the context of the study and the focus of the laboratory, a monocyte-derived cell will be either be called "monocyte-derived DCs" or "macrophages". Because the names we give to cells are often associated with a functional connotation, this is much more than simple semantics. The "name" we give to a population fundamentally changes the perception of its biology and can impact on research design and interpretation. Recent evidence in the ontogeny and transcriptional regulation of DCs and MØs, combined with the identification of DC- and MØ-specific markers has dramatically changed our understanding of their interrelationship in the steady state and inflammation. In steady state, DCs are constantly replaced by circulating blood precursors that arise from committed progenitors in the bone marrow. Similarly, some MØ populations are also constantly replaced by circulating blood monocytes. However, others tissue MØs are derived from embryonic precursors, are seeded before birth and maintain themselves in adults by self-renewal. In inflammation, such differentiation pathways are fundamentally changed and unique monocyte-derived inflammatory cells are generated. Current DC, monocyte and MØ nomenclature does not take into account these new developments and as a consequence is quite confusing. We believe that the field is in need of a fresh view on this topic as well as an upfront debate on DC and MØ nomenclature. Our aim is to bring expert junior and senior scientists to revisit this topic in light of these recent developments. This Research Topic will cover all aspects of DC, monocyte and MØ biology including development, transcriptional regulation, functional specializations, in lymphoid and non-lymphoid tissues, and in both human and mouse models. Given the central position of DCs, monocytes and MØs in tissue homeostasis, immunity and disease, this topic should be of interest to a large spectrum of the biomedical community.