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1.
Elife ; 122024 Apr 23.
Article in English | MEDLINE | ID: mdl-38652107

ABSTRACT

Organisms utilize gene regulatory networks (GRN) to make fate decisions, but the regulatory mechanisms of transcription factors (TF) in GRNs are exceedingly intricate. A longstanding question in this field is how these tangled interactions synergistically contribute to decision-making procedures. To comprehensively understand the role of regulatory logic in cell fate decisions, we constructed a logic-incorporated GRN model and examined its behavior under two distinct driving forces (noise-driven and signal-driven). Under the noise-driven mode, we distilled the relationship among fate bias, regulatory logic, and noise profile. Under the signal-driven mode, we bridged regulatory logic and progression-accuracy trade-off, and uncovered distinctive trajectories of reprogramming influenced by logic motifs. In differentiation, we characterized a special logic-dependent priming stage by the solution landscape. Finally, we applied our findings to decipher three biological instances: hematopoiesis, embryogenesis, and trans-differentiation. Orthogonal to the classical analysis of expression profile, we harnessed noise patterns to construct the GRN corresponding to fate transition. Our work presents a generalizable framework for top-down fate-decision studies and a practical approach to the taxonomy of cell fate decisions.


Subject(s)
Cell Differentiation , Gene Regulatory Networks , Cell Differentiation/genetics , Animals , Hematopoiesis/genetics , Transcription Factors/metabolism , Transcription Factors/genetics , Embryonic Development/genetics , Cell Transdifferentiation/genetics , Humans
2.
Mater Horiz ; 11(10): 2449-2456, 2024 May 20.
Article in English | MEDLINE | ID: mdl-38450711

ABSTRACT

Despite the promising commercial prospects of perovskite solar cells, the issue of lead toxicity continues to hinder their future industrial applications. Here, we report a low-cost and rapidly degraded sulfosuccinic acid-modified polyvinyl alcohol (SMP) coating that prevents lead leakage and enhances device stability without compromising device performance. Even under different strict conditions (simulated heavy rain, acid rain, high temperatures, and competing ions), the coatings effectively prevent lead leakage by over 99%. After 75 days of outdoor exposure, the coating still demonstrates similar lead sequestration efficiency (SQE). In addition, it can be applied to different device structures (n-i-p and p-i-n) and modules, with over 99% SQE, making it a general method for preventing lead leakage.

3.
Adv Healthc Mater ; 13(6): e2303261, 2024 Mar.
Article in English | MEDLINE | ID: mdl-37961920

ABSTRACT

Infectious disease pandemics, including the coronavirus disease 2019 pandemic, have heightened the demand for vaccines. Although parenteral vaccines induce robust systemic immunity, their effectiveness in respiratory mucosae is limited. Considering the crucial role of nasal-associated lymphoid tissue (NALT) in mucosal immune responses, in this study, the intranasal complex composed of G5-BGG and antigen-expressing plasmid DNA (pSP), named G5-BGG/pSP complex, is developed to activate NALT and to promote both systemic and mucosal immune defense. G5-BGG/pSP could traverse mucosal barriers and deliver DNA to the target cells because of its superior nasal retention and permeability characteristics. The intranasal G5-BGG/pSP complex elicits robust antigen-specific immune responses, such as the notable production of IgG antibody against several virus variants. More importantly, it induces elevated levels of antigen-specific IgA antibody and a significant expansion of the lung-resident T lymphocyte population. Notably, the intranasal G5-BGG/pSP complex results in antigen expression and maturation of dendritic cells in nasal mucosae. These findings exhibit the potential of G5-BGG, a novel cationic material, as an effective gene carrier for intranasal vaccines to obtain robust systemic and mucosal immunity.


Subject(s)
COVID-19 , Vaccines , Humans , Immunity, Mucosal , SARS-CoV-2 , COVID-19/prevention & control , DNA , Dendritic Cells
4.
Org Lett ; 25(13): 2172-2177, 2023 Apr 07.
Article in English | MEDLINE | ID: mdl-36946921

ABSTRACT

An expeditious and novel nickel-catalyzed selective arylhydroxylation of unactivated alkenes with arylboronic acids was developed. This protocol is compatible with ß,γ- and γ,δ-alkene amides, including traditionally challenging internal alkenes, to provide important ß-arylethylalcohol scaffolds. The free hydroxyl group in the final product could be smoothly further transformed into other functional groups. Control experiments indicated that the oxygen atom of the hydroxyl group in the product is derived from the oxygen in the air.

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