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精子特异性乳酸脱氢酶-C4对体内和体外同种免疫反应的调节

Modulation of allo-immune responses in vivo and in vitro by sperm specific lactate dehydrogenase-C4.

作者信息

Gupta G S, Kinsky R G

机构信息

Department of Biophysics, Panjab University, Chandigarh, India.

出版信息

Mol Cell Biochem. 1993 Aug 25;125(2):145-51. doi: 10.1007/BF00936443.

Abstract

The role of sperm specific lactate dehydrogenase-C4 (LDH-C4) in allo-immune responses using mixed lymphocyte cultures (MLC) and cytotoxic T cell (CTL) generation in vitro and local graft versus host (LGVH) reaction and allograft enhancement in vivo has been ascertained. LDH was purified from testes (LDH-C4) and kidney (LDH-B4) of C57Bl/Ks mice. MLC and CTL were performed using C57Bl/Ks-anti A/J lymphocytes in presence of 10(-3)-1 micrograms LDH-B4 or LDH-C4 per culture. The MLC and CTL responses showed biphasic action depending on the dose of LDH-C4. Early MLC culture gave significantly low stimulation index at 10(-2)-10(-1) micrograms LDH-C4 as compared to non-treated control cultures. However, the MLC response in presence of LDH-C4 was not different from the LDH-B4 treated one which showed a similar biphasic trend. On the other hand, 51Cr release from YAC-222 target cells was practically abolished by LDH-C4 at 10(-3)-1(-1) micrograms, and this was strikingly different from LDH-B4 or non-treated cultures. LGVH reactivity as performed by using C57Bl/Ks lymphocytes along with LDH-C4 in (C57Bl/Ks x A/J) F1 hybrids indicated a suppression of stimulation index in primary and secondary (i.e. preimmunized in presence of LDH-C4 or LDH-B4) LGVH. Allograft enhancement of Sa I (A/J) in C57Bl/Ks mice in presence of LDH-C4, was delayed slightly but significantly during primary or secondary transplantation reaction.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已确定精子特异性乳酸脱氢酶 - C4(LDH - C4)在体外混合淋巴细胞培养(MLC)和细胞毒性T细胞(CTL)生成、体内局部移植物抗宿主(LGVH)反应及同种异体移植增强等同种免疫反应中的作用。从C57Bl/Ks小鼠的睾丸(LDH - C4)和肾脏(LDH - B4)中纯化LDH。使用C57Bl/Ks - 抗A/J淋巴细胞,在每培养物中存在10^(-3) - 1微克LDH - B4或LDH - C4的情况下进行MLC和CTL实验。MLC和CTL反应呈现双相作用,这取决于LDH - C4的剂量。与未处理的对照培养物相比,在10^(-2) - 10^(-1)微克LDH - C4时,早期MLC培养物的刺激指数显著降低。然而,在LDH - C4存在下的MLC反应与LDH - B4处理的反应没有差异,后者也显示出类似的双相趋势。另一方面,在10^(-3) - 1^(-1)微克时,LDH - C4几乎完全抑制了YAC - 222靶细胞的51Cr释放,这与LDH - B4或未处理的培养物显著不同。在(C57Bl/Ks×A/J)F1杂种中,使用C57Bl/Ks淋巴细胞和LDH - C4进行的LGVH反应表明,在原发性和继发性(即在LDH - C4或LDH - B4存在下预先免疫)LGVH中,刺激指数受到抑制。在LDH - C4存在下,C57Bl/Ks小鼠中Sa I(A/J)的同种异体移植增强在原发性或继发性移植反应期间略有但显著延迟。(摘要截断于250字)

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