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小鼠畸胎瘤细胞系上的H-2 I类抗原表达

H-2 class I antigen expression on mouse teratocarcinoma cell lines.

作者信息

Démant P, Oudshoorn-Snoek M

出版信息

Immunogenetics. 1985;22(6):543-52. doi: 10.1007/BF00430302.

DOI:10.1007/BF00430302
PMID:4077148
Abstract

Immunity against PCC3 teratocarcinoma cells (129, H-2b) was induced in allogeneic (C3H, H-2k) mice by preimmunization with L cells (C3H, H-2k) expressing cosmid-introduced Kb or Db genes, but not with nontransfected L cells. In addition, the growth of PCC3 cells in sublethally irradiated (C3H X B6-H-2bm1)F1 and (C3H X B6-H-2bm13)F1 mice bearing the Kbm1 and Dbm13 mutations, respectively, was either prevented, stopped, or delayed in comparison with the (C3H X B6)F1 (k X b) mice, which failed to reject the PCC3 cells. The teratocarcinoma line OC15S was exceptional because it reacted specifically with Kb- and Db-specific (but not Ib-specific) alloantisera, and because Kb- and Db-specific antibodies could be absorbed by OC15S cells. The subpopulation of OC15S cells bearing the ECMA-7 antigen characteristic for embryonic carcinoma (EC) cells was isolated by the fluorescence-activated cell sorter and was shown to react specifically with Kb- and Db-specific antisera. These experiments show that teratocarcinoma cells express antigens similar or identical to the K- and D-region products of differentiated cells. The lack of expression of class I antigens is thus neither a condition nor a consequence of the pluripotentiality of the EC cells. The exact nature of the major histocompatibility complex antigens on EC cells has yet to be established using the methods of molecular biology and biochemistry.

摘要

通过用表达黏粒导入的Kb或Db基因的L细胞(C3H,H-2k)进行预免疫,在同种异体(C3H,H-2k)小鼠中诱导了对PCC3畸胎瘤细胞(129,H-2b)的免疫,而未转染的L细胞则不能诱导免疫。此外,与未能排斥PCC3细胞的(C3H×B6)F1(k×b)小鼠相比,分别携带Kbm1和Dbm13突变的亚致死剂量照射的(C3H×B6-H-2bm1)F1和(C3H×B6-H-2bm13)F1小鼠中PCC3细胞的生长被阻止、停止或延迟。畸胎瘤细胞系OC15S是个例外,因为它能与Kb和Db特异性(但不是Ib特异性)同种异体抗血清发生特异性反应,并且Kb和Db特异性抗体可被OC15S细胞吸收。通过荧光激活细胞分选仪分离出具有胚胎癌(EC)细胞特征性的携带ECMA-7抗原的OC15S细胞亚群,并显示其能与Kb和Db特异性抗血清发生特异性反应。这些实验表明,畸胎瘤细胞表达的抗原与分化细胞的K区和D区产物相似或相同。因此,I类抗原的缺乏既不是EC细胞多能性的条件,也不是其结果。EC细胞上主要组织相容性复合体抗原的确切性质仍有待用分子生物学和生物化学方法来确定。

相似文献

1
H-2 class I antigen expression on mouse teratocarcinoma cell lines.小鼠畸胎瘤细胞系上的H-2 I类抗原表达
Immunogenetics. 1985;22(6):543-52. doi: 10.1007/BF00430302.
2
Mice coisogenically immunized against H-2 class I antigens on transfected L cells reject transplanted embryonal carcinoma cells.在转染的L细胞上针对H-2 I类抗原进行同基因免疫的小鼠会排斥移植的胚胎癌细胞。
Immunogenetics. 1985;22(6):533-41. doi: 10.1007/BF00430301.
3
Tumor allograft rejection is mainly mediated by CD8+ cytotoxic T lymphocytes stimulated with class I alloantigens in cooperation with CD4+ helper T cells recognizing class II alloantigens.肿瘤同种异体移植排斥主要由受I类同种异体抗原刺激的CD8 + 细胞毒性T淋巴细胞介导,并与识别II类同种异体抗原的CD4 + 辅助性T细胞协同作用。
J Immunol. 1990 Mar 15;144(6):2425-35.
4
Multiple splenic lymphoid cell subpopulations regulate H-2 antigen expression on teratocarcinoma cells in vivo.多种脾淋巴细胞亚群在体内调节畸胎瘤细胞上的H-2抗原表达。
J Immunol. 1983 Jun;130(6):2969-73.
5
Transfection and expression of syngeneic H-2 genes does not reduce malignancy of H-2 negative teratocarcinoma cells in the autologous host.同基因H-2基因的转染和表达不会降低H-2阴性畸胎瘤细胞在自体宿主中的恶性程度。
Cell Immunol. 1990 Jun;128(1):152-64. doi: 10.1016/0008-8749(90)90014-i.
6
Involvement of the K and I regions of the H-2 complex in resistance to hemopoietic allografts.H-2复合体的K区和I区参与对造血异体移植物的抗性。
J Exp Med. 1984 Apr 1;159(4):1070-82. doi: 10.1084/jem.159.4.1070.
7
Induction of class I major histocompatibility complex antigens in human teratocarcinoma cells by interferon without induction of differentiation, growth inhibition, or resistance to viral infection.干扰素诱导人畸胎瘤细胞表达I类主要组织相容性复合体抗原,且不诱导分化、抑制生长或产生抗病毒感染抗性。
Cancer Res. 1987 Feb 1;47(3):740-6.
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Natural killer cells recognize common antigenic motifs shared by H-2Dd, H-2Ld and possibly H-2Dr molecules expressed on bone marrow cells.自然杀伤细胞识别骨髓细胞上表达的H-2Dd、H-2Ld以及可能的H-2Dr分子共有的常见抗原基序。
Int Immunol. 1994 Sep;6(9):1297-306. doi: 10.1093/intimm/6.9.1297.
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Cytotoxic T lymphocyte response to minor H-43a alloantigen in H-43b mice. Privileged H-2Kb restriction to the response is not due to immunodominance or epistatic effect but due to Ir gene function of H-2Kb itself.H-43b小鼠中细胞毒性T淋巴细胞对次要H-43a同种抗原的应答。对该应答的特权性H-2Kb限制并非由于免疫显性或上位效应,而是由于H-2Kb自身的Ir基因功能。
J Immunol. 1988 Jan 1;140(1):44-51.
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Establishment of a pluripotent embryonal carcinoma cell line not expressing SSEA-1 and ECMA-7 phenotypes.
Cell Differ. 1984 Dec;15(2-4):87-92. doi: 10.1016/0045-6039(84)90057-5.

引用本文的文献

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Resistance to 402AX teratocarcinoma involves immunity to minor histocompatibility antigens.对402AX畸胎癌的抗性涉及对次要组织相容性抗原的免疫。
Immunogenetics. 1987;26(1-2):1-5. doi: 10.1007/BF00345447.
2
Embryonal carcinoma cells express Qa and Tla class I genes of the major histocompatibility complex.胚胎癌细胞表达主要组织相容性复合体的Qa和Tla I类基因。
Proc Natl Acad Sci U S A. 1989 Jul;86(13):5084-8. doi: 10.1073/pnas.86.13.5084.
3
Transfected H-2Kb gene as a cause of embryonal carcinoma cell rejection in vivo.转染的H-2Kb基因作为体内胚胎癌细胞排斥反应的一个原因。

本文引用的文献

1
The genetics of teratocarcinoma transplantation: tumor formation in allogeneic hosts by the embryonal carcinoma cell lines F9 and PCC3.畸胎癌移植的遗传学:胚胎癌细胞系 F9 和 PCC3 在同种异体宿主中的肿瘤形成。
Immunogenetics. 1978 Dec;7(1):103-15. doi: 10.1007/BF01843995.
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Strong teratocarcinoma transplantation loci, Gt-1 and Gt-2, flank H-2.强畸胎癌移植位点Gt-1和Gt-2位于H-2侧翼。
Immunogenetics. 1981;13(5):413-9. doi: 10.1007/BF00346022.
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Teratocarcinoma transplantation rejection loci: genetic localization of the Gt-1 locus on chromosome 17 and the expression of alternate alleles.
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Searching for coding sequences in the mammalian genome: the H-2K region of the mouse MHC is replete with genes expressed in embryos.
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H-2 class I and Gt (H-2) antigens are identical: evidence from H-2 mutant mice.H-2 I类抗原与Gt(H-2)抗原相同:来自H-2突变小鼠的证据。
Immunogenetics. 1986;23(4):271-3. doi: 10.1007/BF00373023.
畸胎癌移植排斥位点:17号染色体上Gt-1位点的基因定位及等位基因的表达
Immunogenetics. 1981;13(5):405-12. doi: 10.1007/BF00346021.
4
H-2 negative teratocarcinoma cells become H-2 positive when passaged in genetically resistant host mice.H-2阴性的畸胎瘤细胞在基因抗性宿主小鼠中传代时会变成H-2阳性。
J Immunol. 1981 Jun;126(6):2190-3.
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Biochemistry of the gene products from murine MHC mutants.小鼠主要组织相容性复合体(MHC)突变体基因产物的生物化学
Annu Rev Genet. 1980;14:241-77. doi: 10.1146/annurev.ge.14.120180.001325.
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Crossreactivity between Qa-1 region and H-2K antigens.Qa-1区域与H-2K抗原之间的交叉反应性。
Transplantation. 1983 Apr;35(4):391-3. doi: 10.1097/00007890-198304000-00025.
7
The Qa-1 alloantigens. II. Evidence for the expression of two Qa-1 molecules by the Qa-1d genotype and for cross-reactivity between Qa-1 and H-2K.Qa-1同种异体抗原。II. Qa-1d基因型表达两种Qa-1分子以及Qa-1与H-2K之间存在交叉反应性的证据。
J Immunol. 1983 Mar;130(3):1293-9.
8
Serologic cross-reactivity between Class I MHC molecules and an H-2-linked differentiation antigen as detected by monoclonal antibodies.通过单克隆抗体检测到的I类主要组织相容性复合体分子与H-2连锁分化抗原之间的血清学交叉反应性。
J Exp Med. 1984 Jan 1;159(1):21-40. doi: 10.1084/jem.159.1.21.
9
Teratocarcinoma transplantation antigens are encoded in the H-2 region.畸胎癌移植抗原是在H-2区域编码的。
Immunogenetics. 1983;18(2):137-45. doi: 10.1007/BF00368542.
10
A new determinant, Qa-m208, detected on T lymphocytes and transfected L cells by a Kb-specific monoclonal antibody.一种新的决定簇Qa-m208,通过一种Kb特异性单克隆抗体在T淋巴细胞和转染的L细胞上被检测到。
Immunogenetics. 1984;19(6):461-74. doi: 10.1007/BF00403437.