1997
DOI: 10.1016/s0014-5793(97)00724-2
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BIT, an immune antigen receptor‐like molecule in the brain1

Abstract: We previously found a brain‐specific glycoprotein in the rat brain. It postnatally increases and is rich in the mature brain. We cloned cDNA of this protein. It is composed of a signal peptide, a V‐type immunoglobulin domain, two C1‐type immunoglobulin domains, a transmembrane segment and a cytoplasmic region containing two tyrosine‐based activation motifs (TAM) that are variants of the antigen receptor signaling motifs. The overall structure is similar to those of immune antigen receptors. This molecule, BIT … Show more

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Cited by 77 publications
(29 citation statements)
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“…Toward this end, we used a specific anti-PHPS-1 antibody that binds the extracellular domain to block PHPS-1 functions, presumably by inhibiting the interaction with its ligands. Previous studies demonstrated that anti-PHPS-1 antibodies were able to specifically block PHPS-1-mediated neurite extension (69). Our results showed that incubation of hippocampal slices with anti-PHPS-1 antibody attenuated early phase LTP but had no obvious effects on late phase LTP (Fig.…”
Section: ϫ3supporting
confidence: 61%
“…Toward this end, we used a specific anti-PHPS-1 antibody that binds the extracellular domain to block PHPS-1 functions, presumably by inhibiting the interaction with its ligands. Previous studies demonstrated that anti-PHPS-1 antibodies were able to specifically block PHPS-1-mediated neurite extension (69). Our results showed that incubation of hippocampal slices with anti-PHPS-1 antibody attenuated early phase LTP but had no obvious effects on late phase LTP (Fig.…”
Section: ϫ3supporting
confidence: 61%
“…Our results thus reveal a new example of a functional alteration in cell-cell communication that may contribute to the highly motile and invasive phenotype of malignant melanoma. 2 T. Ogura and T. Noguchi, unpublished data.…”
Section: Fig 4 Inhibition Of Cell Migration By Ligation Of Surface mentioning
confidence: 84%
“…Cells seeded on glass coverslips were washed with phosphate-buffered saline (PBS), fixed with 3% paraformaldehyde in PBS for 20 min, and incubated with 50 mM NH 4 Cl for 10 min. Cells were then permeabilized for 2 min in PBS containing 0.1% Triton X-100 and 1% bovine serum albumin (BSA) before incubation first for 1 h in PBS containing 0.1% Triton X-100, 10% FBS, and 0.5% BSA and then for 1 h with mAb 9E10 to the Myc tag.…”
Section: Methodsmentioning
confidence: 99%