Results : The application of specific optimised conditions induce multiple rounds of memory
B cell proliferation equally across Ig isotypes, differentiation of memory B cells to antibody secreting cells, and importantly do not alter the Ig genotype of the stimulated cells.
Follicular dendritic cells produce IL - 15 that enhances germinal center
B cell proliferation in membrane - bound form.
The major mechanism of B cell suppression by MSCs is attributed partly to the physical contact between MSCs and B cells and in part to the soluble factors released by MSCs; this leads to the blocking of
B cell proliferation in the G0 / G1 phase of the cell cycle with no apoptosis 28, 29, 30.
When GARP was depleted from these cells, there was increase in
B cell proliferation and activation.
«Foxo1 is a tumor suppressor gene, but it promotes
B cell proliferation in the germinal center,» he said.
Not exact matches
B - 1a
cells in meningeal space secrete natural antibodies, which promote the
proliferation of oligodendrocyte precorsors.
Overall, the presence of
B lymphocytes was associated with increased tissue
proliferation, reduced
cell death and a more supportive environment for wound healing.
«Our findings provide direct evidence that
B cells reside in the mouse neonatal brain and promote both oligodendrocyte
proliferation and neuron myelination.
They promote the
proliferation of
B cells that produce highly selective antibodies against invading pathogens while weeding out those that generate potentially harmful ones.
Reviving the BATF levels recovered the
proliferation of Foxo1 - deficient
B cells in the germinal center.
They found substantial differences following influenza vaccination in the production of immune - modulators that determine the type of T -
cell response and in the
proliferation and production of antibodies by
B cells.
For the
proliferation and differentiation to occur,
B cells must cycle between the two zones.
Using mice deficient in Del - 1, they found that the protein promotes
proliferation and differentiation of hematopoetic stem
cells, sending more of these progenitor
cells down a path toward becoming myeloid
cells, such as macrophages and neutrophils, rather than lymphocytes, such as T
cells and
B cells.
Overexpression of GARP reduced the
proliferation and activation of
B cells.
The dark zone is where
B cells undergo
proliferation.
«Role of RNA binding protein in driving cancer, leukemia study reveals: Abnormally expressed in cancer
cells, the protein was found to promote the
proliferation of
B cells in
B -
cell acute lymphoblastic leukemia.»
In the case of IGF2BP3 and
B -
cell leukemia, the overall effect of the RNA binding protein is to promote the
proliferation of
B cells by shifting the expression of a large number of genes, Sanford said.
With this technique, CpG oligonucleotides are only internalized into
B cells that recognize the specific antigen, and these
cells are therefore the only ones in which TLR9 is activated to induce their
proliferation and development into antibody - secreting plasma
cells.
Analogous to bacterial infection, CpG -
B triggers the differentiation of both plasmacytoid and conventional DCs, as well as the
proliferation and activation of
B cells.
More specifically, we found that T
cells from DGKζ − / − and Cbl -
b − / − mice exhibit similar levels of enhanced
proliferation at low levels of TCR stimulation.
Hsiou - Chi Liou and colleagues find that c - Rel, a lymphoid - specific member of the NF - kappaB / Rel family of transcriptional factors, is essential for
B lymphocyte survival and
cell cycle progression, [i] and that it is important for inducible cytokine and cytokine receptor expression and a key regulator of early activation and
proliferation in T
cells.
The addition of IL - 2, as expected, enhanced the
proliferation of WT T
cells, but not completely to levels observed with DGKζ − / − CD8 + T
cells + IL - 2 or to Cbl -
b − / − and DKO CD8 + T
cells (Fig. 3D).
In contrast,
proliferation differences seen between DGKζ − / − or Cbl -
b − / − CD8 + T
cells mostly dissipate upon administration of exogenous IL - 2, which indicates that the enhanced production of IL - 2 in stimulated Cbl -
b − / − CD8 + T
cells is the primary factor responsible for the observed differences between the two genotypes.
MSCs inhibit the
proliferation of
B cells activated with anti-immunoglobulin (Ig) antibodies, anti-CD40L antibody and cytokines (IL - 2 and IL - 4) 31.
Deletion of DGKζ or Cbl -
b comparably enhanced CD8 + T cell functional responses, such as proliferation, production of IFN - γ, and generation of granzyme B when compared with wild type T cells
b comparably enhanced CD8 + T
cell functional responses, such as
proliferation, production of IFN - γ, and generation of granzyme
B when compared with wild type T cells
B when compared with wild type T
cells.
It is involved in the regulation of
B -
cell activation and
proliferation.
DEC1 / STRA13 is a key negative regulator of activation - induced
proliferation of human
B cells highly expressed in anergic
cells
Its binding to DPP4 induces T -
cell proliferation and NF - kappa -
B activation in a T -
cell receptor / CD3 - dependent manner.
Inhibition of
cell proliferation (
B) of MCF7, MCF7 / HER2, or BT474
cells treated for 6 days with F3 - IgG, trastuzumab, or isotype control antibody.
Wnt /
b - catenin / Tcf1 pathway controls mouse embryonic stem
cell cycle progression and
proliferation by regulating the Ink4 / Arf locus.
Abnormally expressed in cancer
cells, the protein was found to promote the
proliferation of
B cells in
B -
cell acute lymphoblastic leukemia
Possible modes of hierarchy alteration are suggested as increased self - renewal (a), dedifferentiation of early progenitor
cells (
b), and blocked
proliferation (c) of ER - α — positive and negative tumors.
These
cells, along with dendritic
cells, recognize the incoming undigested food particles, toxic agents, and bacterial components as foreign invaders, and present them to
cells of the adaptive immune system called T and
B lymphocytes, leading to clonal expansion (
proliferation or multiplication of specific subsets of T and
B cells) and recruitment of more pro-inflammatory immune
cells to the gut through a process called leukocyte homing.
These include a reduction in
B cell differentiation to plasma
cells and a reduced
proliferation of T
cells.