TY  - JOUR
AU  - Samardžić, T.
AU  - Marinković, Dragan
AU  - Danzer, CP
AU  - Gerlach, J
AU  - Nitschke, L.
AU  - Wirth, Thomas
PY  - 2002
UR  - http://rfasper.fasper.bg.ac.rs/handle/123456789/30
AB  - CD22 is a B cell-specific member of the immunoglobulin superfamily and binds to sialic acid. CD22 inhibits B cell receptor signaling. Mice deficient for CD22 show a largely normal B cell development. Here, we have performed a detailed analysis of the splenic B cell population and found that the subset of marginal zone (MZ) B cells was selectively reduced in CD22-deficient mice. CD22-deficient mice showed a lack of TNP-ficoll capturing cells in the MZ and a reduced response to TNP-ficoll, particularly when the antigen was applied intravenously. CD22-deficient B cells showed both enhanced motility as well as enhanced chemotaxis to certain chemokines. The altered chemokine responsiveness or the higher signaling capacity of CD22-deficient B cells may lead to the compromised MZ B cell compartment, as both processes have previously been shown to affect MZ composition.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - European Journal of Immunology
T1  - Reduction of marginal zone B cells in CD22-deficient mice
EP  - 567
IS  - 2
SP  - 561
VL  - 32
DO  - 10.1002/1521-4141(200202)32:2<561::AID-IMMU561>3.0.CO;2-H
ER  - 

@article{
author = "Samardžić, T. and Marinković, Dragan and Danzer, CP and Gerlach, J and Nitschke, L. and Wirth, Thomas",
year = "2002",
abstract = "CD22 is a B cell-specific member of the immunoglobulin superfamily and binds to sialic acid. CD22 inhibits B cell receptor signaling. Mice deficient for CD22 show a largely normal B cell development. Here, we have performed a detailed analysis of the splenic B cell population and found that the subset of marginal zone (MZ) B cells was selectively reduced in CD22-deficient mice. CD22-deficient mice showed a lack of TNP-ficoll capturing cells in the MZ and a reduced response to TNP-ficoll, particularly when the antigen was applied intravenously. CD22-deficient B cells showed both enhanced motility as well as enhanced chemotaxis to certain chemokines. The altered chemokine responsiveness or the higher signaling capacity of CD22-deficient B cells may lead to the compromised MZ B cell compartment, as both processes have previously been shown to affect MZ composition.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "European Journal of Immunology",
title = "Reduction of marginal zone B cells in CD22-deficient mice",
pages = "567-561",
number = "2",
volume = "32",
doi = "10.1002/1521-4141(200202)32:2<561::AID-IMMU561>3.0.CO;2-H"
}

Samardžić, T., Marinković, D., Danzer, C., Gerlach, J., Nitschke, L.,& Wirth, T.. (2002). Reduction of marginal zone B cells in CD22-deficient mice. in European Journal of Immunology
Wiley-V C H Verlag Gmbh, Weinheim., 32(2), 561-567.
https://doi.org/10.1002/1521-4141(200202)32:2<561::AID-IMMU561>3.0.CO;2-H

Samardžić T, Marinković D, Danzer C, Gerlach J, Nitschke L, Wirth T. Reduction of marginal zone B cells in CD22-deficient mice. in European Journal of Immunology. 2002;32(2):561-567.
doi:10.1002/1521-4141(200202)32:2<561::AID-IMMU561>3.0.CO;2-H .

Samardžić, T., Marinković, Dragan, Danzer, CP, Gerlach, J, Nitschke, L., Wirth, Thomas, "Reduction of marginal zone B cells in CD22-deficient mice" in European Journal of Immunology, 32, no. 2 (2002):561-567,
https://doi.org/10.1002/1521-4141(200202)32:2<561::AID-IMMU561>3.0.CO;2-H . .