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Isolation of a cDNA encoding the human CD38 (T10) molecule, a cell surface glycoprotein with an unusual discontinuous pattern of expression during lymphocyte differentiation.
Abstract
A cDNA clone encoding the human lymphocyte differentiation Ag CD38 was isolated from a mixture of four different lymphocyte CDNA libraries expressed transiently in COS cells and screened by panning with mAb. Transfected COS cells expressed a surface protein of Mr 46,000 that was similar to the native CD38 molecule expressed on the B cell line Daudi and the T cell leukemia HPB-ALL and which was recognized by each of the CD38 specific mAb HIT-2, T16, T168, HB7, 5D2, ICO-18, and ICO-20. The CD38 cDNA sequence predicts an unusual 30-kDa polypeptide with a short N-terminal cytoplasmic tail, and a carboxyl-terminal extracellular domain carrying the four potential N-linked glycosylation sites. The absence of significant homology with other known surface Ag including members of the Ig superfamily ruled out the possibility that CD38 was the human homologue of the murine Qa2 molecule as has been suggested previously. PvuII digests of human genomic DNA revealed a polymorphism linked to the CD38 gene.
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“CD38 is ubiquitously expressed by immune cells, and its expression increases during inflammatory conditions8-10.”
From Senescent cells promote tissue NAD+ decline during ageing via the activation of CD38+ macrophages (2020) · cites this paper as [8]
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T Cells and T-Cell Cytokine Transcripts in the Synovial Membrane in Patients with Osteoarthritis
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“CD69 is an early-activation antigen (56), CD25 is an intermediate-activation antigen, CD45RO and HLA class II are late-activation antigens (1), CD38 is an intermediate-activation antigen (19), and CD43 antigen has diverse functions (41).”
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Tazarotene-Induced Gene 1 (TIG1), a Novel Retinoic Acid Receptor-Responsive Gene in Skin
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“It was originally described as a human cell-surface molecule using monoclonal antibody (mAb) T10; however, since then, it has been used as a marker in the study of T and B cell activation and differentiation [1–3].”
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Enzymatic Functions and Structures of CD38 and Homologs
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Ultrastructural localization of CD38 immunoreactivity in rat brain
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CD38 promotes angiotensin II‐induced cardiac hypertrophy
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Roles and mechanisms of the CD38/cyclic adenosine diphosphate ribose/Ca2+signaling pathway
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“As a membrane protein, CD38 contains a single transmembrane domain, a short N-terminal cytoplasmic tail, and a carboxyl-terminal extracellular domain [9].”
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“CD38 is a type II transmembrane glycoprotein, expressed on several leukocytes and early hematopoietic precursor cells (25), that can signal through Raf and ERK activation (26).”
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Localization of the Cyclic ADP-ribose-dependent Calcium Signaling Pathway in Hepatocyte Nucleus
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“In view of its immunological background, CD38 was studied in great detail in hematopoietic cells where its expression has been most appropriately termed ‘discontinuous’ [4].”
BackgroundInfluentialResolving the topological enigma in Ca2+ signaling by cyclic ADP-ribose and NAADP
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“CD38 is a single pass membrane protein consists of a short amino tail, a transmembrane segment and a C-domain (21).”
BackgroundInfluentialHuman lymphocyte antigen CD38 catalyzes the production of cyclic ADP‐ribose
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CD38 ligation induces discrete cytokine mRNA expression in human cultured lymphocytes
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Podestà, M., Zocchi, E., Pitto, A., Usai, C., Franco, L., Bruzzone, S., Guida, L., Bacigalupo, A. P., Scadden, D. T., Walseth, T. F., et al. (2000) · The FASEB Journal · doi:10.1096/fasebj.14.5.680 · Cited by 75
“Both mammalian cyclases are expressed in the bone marrow (BM): CD38 on hemopoietic cells (7, 18) and BST-1 on stromal cells (9); the presence of NAD(1) in plasma and interstitial fluids (16) could enable production of extracellular cADPR in the BM microenvironment.”
BackgroundLack of NK cells in lupus patients with renal involvement
Erkeller-Yüksel, F., Lydyard, P. M., & Isenberg, D. A. (1997) · Lupus · doi:10.1177/096120339700600905 · Cited by 74
Takahashi, K., Kukimoto, I., Tokita, K., Inageda, K., Inoue, S.-I., Kontani, K., Hoshino, S.-I., Nishina, H., Kanaho, Y., & Katada, T. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)00914-u · Cited by 74
Kramer, G., Steiner, G. E., Födinger, D., Fiebiger, E., Rappersberger, C., Binder, S., Hofbauer, J., & Marberger, M. (1995) · The Journal of Urology · doi:10.1016/s0022-5347(01)66733-8 · Cited by 72
A Single Residue at the Active Site of CD38 Determines Its NAD Cyclizing and Hydrolyzing Activities
Graeff, R. M., Munshi, C. B., Aarhus, R., Johns, M. E., & Lee, H. C. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m011299200 · Cited by 71
Kitanaka, A., Ito, C., Nishigaki, H., & Campana, D. (1996) · Blood · doi:10.1182/blood.v88.2.590.bloodjournal882590 · Cited by 70
Zhou, J., Olsen, S., Moldovan, J. B., Fu, X., Sarkar, F. H., Moudgil, V. K., & Callewaert, D. M. (1997) · Cellular Immunology · doi:10.1006/cimm.1997.1138 · Cited by 69
Guida, L., Bruzzone, S., Sturla, L., Franco, L., Zocchi, E., & FLORA, A. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207793200 · Cited by 68
Innate immunity is regulated by CD38, an ecto-enzyme with ADP-ribosyl cyclase activity
Partida‐Sánchez, S., Randall, T. D., & Lund, F. E. (2003) · Microbes and Infection · doi:10.1016/s1286-4579(02)00055-2 · Cited by 68
CD38 Functions Are Regulated Through an Internalization Step
Funaro, A., Reiniš, M., Trubiani, O., Santi, S., Primio, R. D., & Malavasi, F. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.160.5.2238 · Cited by 68
“Cloning and sequencing showed that CD38 has a very short cytoplasmic tail lacking conventional internalization signals and potential phosphorylation sites (38).”
Background
Metadata
- Authors
- Jackson, D. G., & Bell, J. I.
- Affiliations
- John Radcliffe Hospital (GB)
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 1990-04-01
- Volume
- 144
- Issue
- 7
- Pages
- 2811-2815
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- OpenAlex
- W1566643819
- Cited by
- 343
- References
- 0
- Citations by year
- 2026: 5 · 2025: 3 · 2024: 4 · 2023: 2 · 2022: 10 · 2021: 3 · 2020: 13 · 2019: 9 · 2018: 8 · 2017: 6 · 2016: 6 · 2015: 5 · 2014: 6 · 2013: 5 · 2012: 10
- FWCI
- 3.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Monoclonal and Polyclonal Antibodies Research
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Keywords
- CD38, lymphocyte differentiation antigens, cDNA cloning, cell surface glycoproteins, lymphocyte differentiation, B cells, T cells, monoclonal antibodies, N-glycosylation, cytoplasmic tail, genetic polymorphism, Daudi cells
- MeSH terms
- Amino Acid Sequence, Antigens, Differentiation, Base Sequence, Cloning, Molecular, DNA, Genes, Humans, Lymphocytes, Membrane Glycoproteins, Molecular Sequence Data, Molecular Weight, Solubility, Transfection, Blotting, Southern, Antigens, CD, Gene Expression, ADP-ribosyl Cyclase, ADP-ribosyl Cyclase 1
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