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  • 1
    Electronic Resource
    Electronic Resource
    Oxford UK : Blackwell Science Ltd
    Weed research 42 (2002), S. 0 
    ISSN: 1365-3180
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: The germination ecology of four annual Bromus species, which differ in weediness on arable land in southern Sweden, was investigated. The most problematic species is Bromus sterilis, while Bromus hordeaceus frequently occurs on arable land. In contrast, Bromus arvensis is a rare weed, and Bromus tectorum is found infrequently in fields despite being a widespread ruderal species. Five experiments were conducted to identify germination characteristics that could explain differences in habitat and abundance: (i) intraspecific variation in dormancy level; (ii) germination response to different light conditions; (iii) light and temperature interactions at germination; (iv) timing of seedling emergence; and (v) seed persistence in soil. Bromus sterilis and B. tectorum behaved similarly in all tests. For both these species, there were large differences in dormancy level among populations and strong inhibition of germination by light. In addition, emergence from seeds sown on the soil surface was both delayed and reduced compared with buried seeds. In contrast, B. hordeaceus and B. arvensis showed generally weak dormancy, and germination was only slightly inhibited by light. It was concluded that germination characteristics alone do not explain the differences in weediness between these four species.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2020-12-14
    Description: While Th1 and Th17 T effector cells are pathogenic drivers of glomerulonephritis (GN), regulatory T cells (Tregs) potently protect from renal tissue injury. Recently, it has become evident that different Treg subtypes exist. Among these are lineage specific Treg1 and Treg17 cells, which are specialized to down regulate either Th1 or Th17 T effector cell responses. Interestingly, programming of specialized Tregs and the corresponding T helper effector cells depend on the same lineage specific master transcription factors Tbet (Th1/Treg1) and STAT3 (Th17/Treg17). Furthermore, early control of T effector cell priming in secondary lymphoid organs by specialized Tregs was described. One central mechanism of T effector cell control by the corresponding Treg subtype seems to be expression of the same chemokine receptor repertoire, which facilitates their co-localization. More recently, another intriguing Treg subset was identified, which expresses Foxp3 together with the Th17 characteristic transcription factor RORγt. While these Foxp3+RORγt+ Tregs were shown to be highly immunosuppressive, studies in GN also identified pro-inflammatory potential via secretion of IL-17. Many questions regarding this unusual Treg subset remain, including their origin, stability, and mechanisms of action. Further characterization of the renal Treg landscape during GN will help to identify novel immunosuppressive mechanisms and develop successful Treg-directed therapies. In this review, we summarize the currently available data about specialized Treg subsets and discuss their role in GN.
    Print ISSN: 0302-766X
    Electronic ISSN: 1432-0878
    Topics: Biology , Medicine
    Published by Springer
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