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Biology subjects

Chen, Z. W.

Publications and source records attributed to Chen, Z. W..

2 recordsLinked to original sources

Proteomic analysis reveals distinct germination strategies in polymorphic fruits of Haloxylon ammodendron

Fruit polymorphism, the production of multiple fruit morphotypes within a species, is an adaptive bet-hedging strategy in variable environments. However, researches about perennial plant and the adaptive mechanisms are not well understood. Haloxylon ammodendron, a constructive desert shrub, exhibits three fruit morphotypes: YY (yellow wings with yellow pericarp), YP (yellow wings with pink pericarp), and PP (pink wings with pink pericarp). We investigated their ecophysiological and molecular mechanisms through germination assays under salt and drought stress, combined with proteomic analysis. YP consistently showed the highest germination percentage (GP) and germination rate index (GRI) under stress, while PP displayed well germination success under low salinity and well-watered conditions (GP=32.7%, 36.7%; GRI=0.018, 0.020), but significantly impaired viability under stress (GP=12.7%, 12.0%; GRI=0.006, 0.006). Proteomics identified 721 differentially expressed proteins (DEPs), with the most (662) between YP and PP, linked to stress response and germination. YPs high abundance of stress-resistant proteins enabled rapid germination, whereas PPs delayed germination aligns with a persistent seed bank strategy. This polymorphism promotes niche differentiation: YP ensures quick colonization, PP enhances long-term resilience, and YY offers an intermediate strategy. Our findings reveal molecular-ecological adaptations in H. ammodendron, aiding targeted germplasm use for desert restoration.

plant biology↗

CTLA-4 blockade reverses the Foxp3+ T-regulatory-cell suppression of anti-tuberculosis T-cell effector responses

BackgroundsIt has been well described that Foxp3+ T regulatory (Treg) cells suppress immune responses and that murine cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) can control the function of Foxp3+Treg cells. However, it remains unknown about the role of CTLA-4 pathway in Treg suppression of T cell responses in tuberculosis (TB). MethodsWe assessed TB-driven changes in CTLA-4-expressing Foxp3+ Treg and conducted CTLA-4 blocking mechanistic studies ex vivo in 126 subjects with active TB, latent TB or uninfected statuses. ResultsFrequencies of CTLA-4-expressing Treg cells were increased in the circulation of pulmonary TB patients and in the pleural compartment of TB pleuritis. Six-month anti-TB treatment significantly reduced CTLA-4+ Treg subset. Notably, antibody blocking of CTLA-4 pathway (CTLA-4 blockade) reversed the ability of Treg cells to suppress anti-TB Th1 responses and abrogated the Treg-mediated suppression of TB antigen-stimulated proliferative response. The CTLA-4 blockade reversed the Treg suppression of the ability of T cells to restrict intracellular BCG and M. tuberculosis growth in macrophages. InterpretationThe study uncovered previously-unreported observations implicating that the CTLA-4 blockade abrogates the capability of Treg cells to suppress anti-TB immune responses or immunity. Findings support the rationale for exploring the CTLA-4 blockade as potential host-directed therapy against TB. FundThis work is supported in part by the National Natural Science Foundation of China (30901277, 81671553, 81501359), and the Key Technologies Research and Development Program for Infectious Diseases of China (2017ZX10201302-004).

immunology↗