scholarly journals Spatio-temporal localization of selected pectic and arabinogalactan protein epitopes and the ultrastructural characteristics of explant cells that accompany the changes in the cell fate during somatic embryogenesis in Arabidopsis thaliana

2018 ◽  
Vol 127 ◽  
pp. 573-589 ◽  
Author(s):  
Izabela Potocka ◽  
Kamila Godel ◽  
Izabela Dobrowolska ◽  
Ewa U. Kurczyńska
Keyword(s):  
Arabidopsis Thaliana ◽  
Somatic Embryogenesis ◽  
Cell Fate ◽  
Arabinogalactan Protein ◽  
Ultrastructural Characteristics ◽  
Spatio Temporal ◽  
Temporal Localization

scholarly journals Cell Wall Composition as a Marker of the Reprogramming of the Cell Fate on the Example of a Daucus carota (L.) Hypocotyl in Which Somatic Embryogenesis Was Induced

2020 ◽  
Vol 21 (21) ◽  
pp. 8126
Author(s):  
Michał Kuczak ◽  
Ewa Kurczyńska
Keyword(s):  
Somatic Embryogenesis ◽  
Cell Fate ◽  
Cell Walls ◽  
Arabinogalactan Proteins ◽  
Cell Wall Composition ◽  
Cell Reprogramming ◽  
Daucus Carota L ◽  
Negative Marker ◽  
Spatio Temporal ◽  
Wall Components

Changes in the composition of the cell walls are postulated to accompany changes in the cell’s fate. We check whether there is a relationship between the presence of selected pectic, arabinogalactan proteins (AGPs), and extensins epitopes and changes in cell reprogramming in order to answer the question of whether they can be markers accompanying changes of cell fate. Selected antibodies were used for spatio-temporal immunolocalization of wall components during the induction of somatic embryogenesis. Based on the obtained results, it can be concluded that (1) the LM6 (pectic), LM2 (AGPs) epitopes are positive markers, but the LM5, LM19 (pectic), JIM8, JIM13 (AGPs) epitopes are negative markers of cells reprogramming to the meristematic/pluripotent state; (2) the LM8 (pectic), JIM8, JIM13, LM2 (AGPs) and JIM11 (extensin) epitopes are positive markers, but LM6 (pectic) epitope is negative marker of cells undergoing detachment; (3) JIM4 (AGPs) is a positive marker, but LM5 (pectic), JIM8, JIM13, LM2 (AGPs) are negative markers for pericycle cells on the xylem pole; (4) LM19, LM20 (pectic), JIM13, LM2 (AGPs) are constitutive wall components, but LM6, LM8 (pectic), JIM4, JIM8, JIM16 (AGPs), JIM11, JIM12 and JIM20 (extensins) are not constitutive wall components; (5) the extensins do not contribute to the cell reprogramming.

scholarly journals High level expression of transgenes by use of 5^|^#8242;-untranslated region of the Arabidopsis thaliana arabinogalactan-protein 21 gene in dicotyledons

2012 ◽  
Vol 29 (3) ◽  
pp. 319-322 ◽  
Author(s):  
Takeshi Matsui ◽  
Hideyuki Matsuura ◽  
Kazutoshi Sawada ◽  
Eiji Takita ◽  
Satoko Kinjo ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Untranslated Region ◽  
Arabinogalactan Protein ◽  
High Level Expression ◽  
High Level

Deep Learning for Spatio-Temporal Localization of Temporomandibular Joint in Ultrasound Videos

2021 ◽  
Author(s):  
Kristina Belikova ◽  
Aleksandra Zailer ◽  
Svetlana V. Tekucheva ◽  
Sergey N. Ermoljev ◽  
Dmitry V. Dylov
Keyword(s):  
Deep Learning ◽  
Temporomandibular Joint ◽  
Spatio Temporal ◽  
Temporal Localization

scholarly journals Hormonal Regulation of Stem Cell Proliferation at the Arabidopsis thaliana Root Stem Cell Niche

2021 ◽  
Vol 12 ◽  
Author(s):  
Mónica L. García-Gómez ◽  
Adriana Garay-Arroyo ◽  
Berenice García-Ponce ◽  
María de la Paz Sánchez ◽  
Elena R. Álvarez-Buylla
Keyword(s):  
Cell Proliferation ◽  
Arabidopsis Thaliana ◽  
Stem Cell ◽  
Cell Fate ◽  
Regulatory Network ◽  
Hormonal Regulation ◽  
Stem Cell Niche ◽  
Quiescent Center ◽  
Root Stem Cell ◽  
Cell Niche

The root stem cell niche (SCN) of Arabidopsis thaliana consists of the quiescent center (QC) cells and the surrounding initial stem cells that produce progeny to replenish all the tissues of the root. The QC cells divide rather slowly relative to the initials, yet most root tissues can be formed from these cells, depending on the requirements of the plant. Hormones are fundamental cues that link such needs with the cell proliferation and differentiation dynamics at the root SCN. Nonetheless, the crosstalk between hormone signaling and the mechanisms that regulate developmental adjustments is still not fully understood. Developmental transcriptional regulatory networks modulate hormone biosynthesis, metabolism, and signaling, and conversely, hormonal responses can affect the expression of transcription factors involved in the spatiotemporal patterning at the root SCN. Hence, a complex genetic–hormonal regulatory network underlies root patterning, growth, and plasticity in response to changing environmental conditions. In this review, we summarize the scientific literature regarding the role of hormones in the regulation of QC cell proliferation and discuss how hormonal signaling pathways may be integrated with the gene regulatory network that underlies cell fate in the root SCN. The conceptual framework we present aims to contribute to the understanding of the mechanisms by which hormonal pathways act as integrators of environmental cues to impact on SCN activity.

scholarly journals Purification of pseudopodia from polarized cells reveals redistribution and activation of Rac through assembly of a CAS/Crk scaffold

2002 ◽  
Vol 156 (4) ◽  
pp. 725-736 ◽  
Author(s):  
Samuel Y. Cho ◽  
Richard L. Klemke
Keyword(s):  
Focal Adhesion ◽  
Feedback Loop ◽  
Kinase Activity ◽  
Cell Polarization ◽  
Molecular Scaffold ◽  
Rac1 Activity ◽  
Polarized Cells ◽  
Focal Adhesion Kinase Activity ◽  
Spatio Temporal ◽  
Temporal Localization

Initiation of cell migration requires morphological polarization with formation of a dominant leading pseudopodium and rear compartment. A molecular understanding of this process has been limited, due to the inability to biochemically separate the leading pseudopodium from the rear of the cell. Here we examine the spatio-temporal localization and activation of cytoskeletal-associated signals in purified pseudopodia directed to undergo growth or retraction. Pseudopodia growth requires assembly of a p130Crk-associated substrate (CAS)/c-CrkII (Crk) scaffold, which facilitates translocation and activation of Rac1. Interestingly, Rac1 activation then serves as a positive-feedback loop to maintain CAS/Crk coupling and pseudopodia extension. Conversely, disassembly of this molecular scaffold is critical for export and down regulation of Rac1 activity and induction of pseudopodia retraction. Surprisingly, the uncoupling of Crk from CAS during pseudopodium retraction is independent of changes in focal adhesion kinase activity and CAS tyrosine phosphorylation. These findings establish CAS/Crk as an essential scaffold for Rac1-mediated pseudopodia growth and retraction, and illustrate spatio-temporal segregation of cytoskeletal signals during cell polarization.

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