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The ion channel TRPV5 regulates B-cell signaling and activation
by
Mahtani, Trisha
, Benedict, Leshawn
, Brecier, Aurelie
, Ghasemlou, Nader
, Treanor, Bebhinn
, Smith, L. K.
, Sheth, Hena
in
1-Phosphatidylinositol 3-kinase
/ Animals
/ Antibodies
/ Antigens
/ B cells
/ B-cell receptor
/ B-Lymphocytes - immunology
/ B-Lymphocytes - metabolism
/ Calcium (reticular)
/ Calcium - metabolism
/ Calcium channels
/ Calcium influx
/ Calcium permeability
/ Calcium Signaling
/ Calcium signalling
/ Cell activation
/ Cell growth
/ Cell signaling
/ CRISPR
/ Endoplasmic reticulum
/ Humoral immunity
/ Immunization
/ Immunology
/ ion channels
/ Lymphocyte Activation - immunology
/ Lymphocytes B
/ Mice
/ Mice, Inbred C57BL
/ Mice, Knockout
/ Orai1 protein
/ Pathogens
/ Proteins
/ Receptors, Antigen, B-Cell - immunology
/ Receptors, Antigen, B-Cell - metabolism
/ RhoA protein
/ Signal Transduction
/ signaling
/ Software
/ Stem cells
/ transient receptor potential channel
/ Transient receptor potential proteins
/ TRPV Cation Channels - genetics
/ TRPV Cation Channels - metabolism
/ TRPV5
2024
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The ion channel TRPV5 regulates B-cell signaling and activation
by
Mahtani, Trisha
, Benedict, Leshawn
, Brecier, Aurelie
, Ghasemlou, Nader
, Treanor, Bebhinn
, Smith, L. K.
, Sheth, Hena
in
1-Phosphatidylinositol 3-kinase
/ Animals
/ Antibodies
/ Antigens
/ B cells
/ B-cell receptor
/ B-Lymphocytes - immunology
/ B-Lymphocytes - metabolism
/ Calcium (reticular)
/ Calcium - metabolism
/ Calcium channels
/ Calcium influx
/ Calcium permeability
/ Calcium Signaling
/ Calcium signalling
/ Cell activation
/ Cell growth
/ Cell signaling
/ CRISPR
/ Endoplasmic reticulum
/ Humoral immunity
/ Immunization
/ Immunology
/ ion channels
/ Lymphocyte Activation - immunology
/ Lymphocytes B
/ Mice
/ Mice, Inbred C57BL
/ Mice, Knockout
/ Orai1 protein
/ Pathogens
/ Proteins
/ Receptors, Antigen, B-Cell - immunology
/ Receptors, Antigen, B-Cell - metabolism
/ RhoA protein
/ Signal Transduction
/ signaling
/ Software
/ Stem cells
/ transient receptor potential channel
/ Transient receptor potential proteins
/ TRPV Cation Channels - genetics
/ TRPV Cation Channels - metabolism
/ TRPV5
2024
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The ion channel TRPV5 regulates B-cell signaling and activation
by
Mahtani, Trisha
, Benedict, Leshawn
, Brecier, Aurelie
, Ghasemlou, Nader
, Treanor, Bebhinn
, Smith, L. K.
, Sheth, Hena
in
1-Phosphatidylinositol 3-kinase
/ Animals
/ Antibodies
/ Antigens
/ B cells
/ B-cell receptor
/ B-Lymphocytes - immunology
/ B-Lymphocytes - metabolism
/ Calcium (reticular)
/ Calcium - metabolism
/ Calcium channels
/ Calcium influx
/ Calcium permeability
/ Calcium Signaling
/ Calcium signalling
/ Cell activation
/ Cell growth
/ Cell signaling
/ CRISPR
/ Endoplasmic reticulum
/ Humoral immunity
/ Immunization
/ Immunology
/ ion channels
/ Lymphocyte Activation - immunology
/ Lymphocytes B
/ Mice
/ Mice, Inbred C57BL
/ Mice, Knockout
/ Orai1 protein
/ Pathogens
/ Proteins
/ Receptors, Antigen, B-Cell - immunology
/ Receptors, Antigen, B-Cell - metabolism
/ RhoA protein
/ Signal Transduction
/ signaling
/ Software
/ Stem cells
/ transient receptor potential channel
/ Transient receptor potential proteins
/ TRPV Cation Channels - genetics
/ TRPV Cation Channels - metabolism
/ TRPV5
2024
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The ion channel TRPV5 regulates B-cell signaling and activation
Journal Article
The ion channel TRPV5 regulates B-cell signaling and activation
2024
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Overview
B-cell activation triggers the release of endoplasmic reticulum calcium stores through the store-operated calcium entry (SOCE) pathway resulting in calcium influx by calcium release-activated calcium (CRAC) channels on the plasma membrane. B-cell-specific murine knockouts of SOCE do not impact humoral immunity suggesting that alternative channels may be important.
We identified a member of the calcium-permeable transient receptor potential (TRP) ion channel family, TRPV5, as a candidate channel expressed in B cells by a quantitative polymerase chain reaction (qPCR) screen. To further investigate the role of TRPV5 in B-cell responses, we generated a murine TRPV5 knockout (KO) by CRISPR-Cas9.
We found TRPV5 polarized to B-cell receptor (BCR) clusters upon stimulation in a PI3K-RhoA-dependent manner. TRPV5 KO mice have normal B-cell development and mature B-cell numbers. Surprisingly, calcium influx upon BCR stimulation in primary TRPV5 KO B cells was not impaired; however, differential expression of other calcium-regulating proteins, such as ORAI1, may contribute to a compensatory mechanism for calcium signaling in these cells. We demonstrate that TRPV5 KO B cells have impaired spreading and contraction in response to membrane-bound antigen. Consistent with this, TRPV5 KO B cells have reduced BCR signaling measured through phospho-tyrosine residues. Lastly, we also found that TRPV5 is important for early T-dependent antigen specific responses post-immunization.
Thus, our findings identify a role for TRPV5 in BCR signaling and B-cell activation.
Publisher
Frontiers Media SA,Frontiers Media S.A
Subject
1-Phosphatidylinositol 3-kinase
/ Animals
/ Antigens
/ B cells
/ CRISPR
/ Lymphocyte Activation - immunology
/ Mice
/ Proteins
/ Receptors, Antigen, B-Cell - immunology
/ Receptors, Antigen, B-Cell - metabolism
/ Software
/ transient receptor potential channel
/ Transient receptor potential proteins
/ TRPV Cation Channels - genetics
/ TRPV Cation Channels - metabolism
/ TRPV5
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