组织蛋白酶S

组织蛋白酶S
已知的結構
PDB	直系同源搜索: PDBe RCSB
PDBID列表
	1GLO、1MS6、1NPZ、1NQC、2C0Y、2F1G、2FQ9、2FRA、2FRQ、2FT2、2FUD、2FYE、2G6D、2G7Y、2H7J、2HH5、2HHN、2HXZ、2OP3、2R9M、2R9N、2R9O、3IEJ、3KWN、3MPE、3MPF、3N3G、3N4C、3OVX、4P6E、4P6G
識別號
别名	CTSS；, cathepsin S
外部ID	OMIM：116845 MGI：107341 HomoloGene：20867 GeneCards：CTSS
為以下藥物的標靶
	odanacatib
基因位置（人类）
染色体	1號染色體
终止	150,765,957 bp
基因位置（小鼠）
染色体	小鼠3号染色体
终止	95,463,714 bp
RNA表达模式
	; ;
	查阅更多表达数据
基因本體
分子功能	• fibronectin binding; • 半胱氨酸型肽酶活性; • collagen binding; • 肽酶活性; • cysteine-type endopeptidase activity; • laminin binding; • 水解酶活性; • proteoglycan binding; • serine-type endopeptidase activity;
細胞組分	• 細胞內膜結合細胞器; • 細胞外區域; • endolysosome lumen; • lysosomal lumen; • 溶酶体; • 細胞外空間; • tertiary granule lumen; • ficolin-1-rich granule lumen; • collagen-containing extracellular matrix; • 晚期内吞体;
生物學過程	• positive regulation of cation channel activity; • antigen processing and presentation; • adaptive immune response; • antigen processing and presentation of exogenous peptide antigen via MHC class II; • protein processing; • extracellular matrix disassembly; • 蛋白酶解; • toll-like receptor signaling pathway; • antigen processing and presentation of peptide antigen; • 免疫反应; • cellular response to thyroid hormone stimulus; • collagen catabolic process; • proteolysis involved in cellular protein catabolic process; • basement membrane disassembly; • response to acidic pH; • neutrophil degranulation;
	Sources:Amigo / QuickGO
直系同源
	1520
	13040
	ENSG00000163131
	ENSMUSG00000038642
	P25774
	O70370
	NM_004079; NM_001199739
	NM_001267695; NM_021281
	NP_001186668; NP_004070
	NP_001254624; NP_067256
	維基數據
檢視/編輯人類	檢視/編輯小鼠

组织蛋白酶S（英文：Cathepsin S）是人类体内由CTSS基因编码的蛋白质^[6]。该基因存在利用多腺苷酸化信号的转录变体。^[6]

组织蛋白酶S是木瓜样蛋白酶（英语：Papain-like protease）肽酶C1家族的成员^[7]。它是一种溶酶体半胱氨酸蛋白酶，可参与将抗原蛋白降解为肽以呈递给MHC II类分子。^[8]^[9]组织蛋白酶S可以在肺泡巨噬细胞的广泛的pH值范围内作为弹性蛋白酶发挥作用。^[10]^[11]

作用[编辑]

虽然人们早已知道组织蛋白酶S在抗原呈递中的作用^[12]^[13]，但现在更加深入地了解到组织蛋白酶S在瘙痒和疼痛或伤害感受中起地作用。^[14] 伤害性活性是由组织蛋白酶S通过激活G蛋白偶联受体家族的蛋白酶激活受体（英语：Protease-activated receptor）2和4作为信号分子而产生的。^[15]

组织蛋白酶S由抗原呈递细胞表达，包括巨噬细胞、B细胞、树突状细胞和小胶质细胞。^[16]^[17]组织蛋白酶S也由一些上皮细胞表达。^[18]在用γ-干扰素刺激后，它在人角质形成细胞中的表达有着显着的增加，并且由于促炎性细胞因子的刺激，它在银屑病角质形成细胞中的表达也会升高。^[19]相反，皮质胸腺上皮细胞（英语：Cortical thymic epithelial cells）不表达组织蛋白酶S。^[20]^[21]

虽然许多溶酶体蛋白酶最适合的pH值是酸性的^[22]^[23]^[24]，但组织蛋白酶S是一个例外。组织蛋白酶S在中性pH值下保持催化活性，而pH值5.0到7.5之间是组织蛋白酶S的最佳pH值范围。^[25]^[26]由于稳定性问题，许多溶酶体蛋白酶被困在溶酶体内。相反，组织蛋白酶S可以保持稳定并在溶酶体外具有生理作用。^[27]^[28]包括巨噬细胞和小胶质细胞在内的免疫细胞会分泌组织蛋白酶S以响应炎症介质，包括脂多糖^[29]、促炎性细胞因子^[30]和中性粒细胞。^[31]在体外，组织蛋白酶S在3M尿素存在下可以保留一些酶活性。^[32]组织蛋白酶S作为酶原产生并通过加工被激活。^[33]

组织蛋白酶S的活性受到其内源性抑制剂——胱抑素C的严格调节，胱抑素C在抗原呈递中也有作用。^[34]^[35]与胱抑素C相比，胱抑素A和胱抑素B的活性较低。^[36]

组织蛋白酶S的活性切割位点 -(-Val-Val-Arg-)- 应该有至少两个氨基酸从每一侧包围它。^[37]

在抗原呈现中的作用[编辑]

组织蛋白酶S在抗原呈现中起关键作用。MHC II类分子与小肽片段相互作用，以在抗原呈现免疫细胞表面呈递。组织蛋白酶S参与阻止抗原加载到复合物中的恒定链（英语：CD74）（li chain）的降解。这种降解发生在溶酶体中。按时间顺序，组织蛋白酶S的作用遵循着天冬氨酸蛋白酶进行的两次切割。组织蛋白酶S切割Ii的残余片段（IiP1）并留下一小部分碎片，称为CLIP。它与复合物有直接的联系。

Ii的蛋白水解很重要，因为它有助于CLIP从MHC II上解离，以便复合物得以加载选定的抗原。加载抗原后，MHC II分子移动到细胞表面。因此，我们可以推测组织蛋白酶S的过度表达可能会导致Ii的过早降解、MHC II的临时加载和自身的免疫攻击。相反，组织蛋白酶S的抑制将导致Ii的降解、将抗原加载到MHC II中的延迟以及在细胞表面上MHC II中未切割li的片段的不适当存在，并且它会削弱免疫反应。例如，这种MHC II不会非常有效地诱导T细胞的增殖。

在巨噬细胞中，组织蛋白酶S可以被组织蛋白酶F取代。

在细胞外基质降解中的作用[编辑]

分泌出来的组织蛋白酶S会切割一些细胞外基质（ECM）蛋白。组织蛋白酶S被认为是已知最有效的弹性蛋白酶。组织蛋白酶S底物列表包括层粘连蛋白、纤连蛋白、弹性蛋白、骨钙蛋白和一些胶原蛋白。它还切割基底膜的硫酸软骨素、硫酸乙酰肝素和蛋白聚糖。组织蛋白酶S由于其弹性溶解和胶原溶解活性而在血管通透性（英语：Vascular permeability）和血管新生中发挥积极作用。例如，组织蛋白酶S对层粘连蛋白5的切割会导致促血管生成肽。组织蛋白酶S的表达可由肿瘤细胞分泌的促炎因子触发。

在癌变中，组织蛋白酶S会促进肿瘤生长。

在细胞因子调节中的作用[编辑]

组织蛋白酶S的表达和活性也在银屑病患者的皮肤中被上调。它是否在引起银屑病具有明确的作用尚不清楚，但在同一项研究中，它被证明可以特别切割和激活银屑病相关的促炎细胞因子IL-36γ（英语：IL36G）^[30]

伤害感受[编辑]

组织蛋白酶S在伤害感受（英语：Nociception）中起作用，包括瘙痒和胃肠道疼痛。组织蛋白酶S导致瘙痒和疼痛的机制与蛋白酶激活受体2（英语：Protease-activated receptor 2）和4的能力一致。^[38]^[39]

组织蛋白酶S抑制剂[编辑]

组织蛋白酶S的合成抑制剂参与了许多针对包括类风湿性关节炎在内的免疫疾病的临床前研究。目前，他们中至少有一个参与了银屑病的临床试验。LHVS（吗啉脲-亮氨酸-高苯丙氨酸-乙烯基砜-苯基）是研究最广泛的组织蛋白酶S的合成抑制剂。LHVS的半抑制浓度（英语：IC50）约为5nM。 LHVS对组织蛋白酶S的抑制作用已被证明。它在创伤性脑损伤后具有神经保护作用。^[40]商业抑制剂清单还包括紫斑肽（乙酰-Leu-Val-CHO）和其他抑制剂。

临床意义[编辑]

组织蛋白酶S已被证明是IV型星形细胞瘤（英语：Astrocytoma）（胶质母细胞瘤）患者的重要预后因素，其抑制作用显示患者平均存活时间延长了5个月。这是因为半胱氨酸酶不能再与其他蛋白酶一起作用来分解脑细胞外基质。这样肿瘤的扩散就停止了。科学家们宣布，这种酶可能可以预测死亡，因为它已被证明与心脏病和癌症有关。

参见[编辑]

组织蛋白酶

参考文献[编辑]

^ 對Cathepsin S起作用的藥物；在維基數據上查看/編輯參考.
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^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Mouse PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.
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拓展阅读[编辑]

Shi GP, Munger JS, Meara JP, Rich DH, Chapman HA. Molecular cloning and expression of human alveolar macrophage cathepsin S, an elastinolytic cysteine protease. The Journal of Biological Chemistry. April 1992, 267 (11): 7258–7262. PMID 1373132. doi:10.1016/S0021-9258(18)42513-6 .
Wang J, Tsirka SE. Contribution of extracellular proteolysis and microglia to intracerebral hemorrhage. Neurocritical Care. 2005, 3 (1): 77–85. PMID 16159103. S2CID 26759184. doi:10.1385/NCC:3:1:077.
Wiederanders B, Brömme D, Kirschke H, von Figura K, Schmidt B, Peters C. Phylogenetic conservation of cysteine proteinases. Cloning and expression of a cDNA coding for human cathepsin S. The Journal of Biological Chemistry. July 1992, 267 (19): 13708–13713. PMID 1377692. doi:10.1016/S0021-9258(18)42271-5 .
Ritonja A, Colić A, Dolenc I, Ogrinc T, Podobnik M, Turk V. The complete amino acid sequence of bovine cathepsin S and a partial sequence of bovine cathepsin L. FEBS Letters. June 1991, 283 (2): 329–331. PMID 2044774. doi:10.1016/0014-5793(91)80620-I .
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Luke C, Schick C, Tsu C, Whisstock JC, Irving JA, Brömme D, et al. Simple modifications of the serpin reactive site loop convert SCCA2 into a cysteine proteinase inhibitor: a critical role for the P3' proline in facilitating RSL cleavage. Biochemistry. June 2000, 39 (24): 7081–7091. PMID 10852705. doi:10.1021/bi000050g.

外部链接[编辑]

The MEROPS online database for peptidases and their inhibitors: C01.034 （页面存档备份，存于互联网档案馆）
Template:BRENDA
PDB中UniProt可用的所有結構信息之概述：P25774 (Cathepsin S) 在PDBe-KB（英语：PDBe-KB）。

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[refGRCm38Ensembl-3] 3.0 ^3.1 ^3.2 GRCm38: Ensembl release 89: ENSMUSG00000038642 - Ensembl, May 2017

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