CEACAM1 in vascular homeostasis and inflammation

被引:0
作者
Gotz, Lisa [1 ]
Rueckschloss, Uwe [1 ]
Ergun, Suleyman [1 ]
Kleefeldt, Florian [1 ]
机构
[1] Univ Wurzburg, Inst Anat & Cell Biol, Wurzburg, Germany
关键词
cardiovascular; CEACAM1; homeostasis; inflammation; CELL-ADHESION MOLECULE-1; CARCINOEMBRYONIC ANTIGEN FAMILY; BILIARY GLYCOPROTEIN; HOMOPHILIC ADHESION; STRUCTURAL-ANALYSIS; CYTOPLASMIC DOMAIN; ANGIOGENIC FACTOR; CEA; EXPRESSION; DELETION;
D O I
10.1111/eci.14345
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionThe glycoprotein Carcinoembryonic Antigen-related Cell Adhesion Molecule 1 (CEACAM1), also known as CD66a, is a member of the immunoglobulin superfamily. It is expressed in a variety of tissues including epithelial, immune, as well as endothelial cells, and is crucial to diverse physiological and pathological mechanisms. This review aims to provide a comprehensive understanding of CEACAM1's multifaceted roles in vascular biology and inflammatory processes.MethodsDirected literature research was conducted using databases, such as PubMed, and relevant studies were categorized based on the physiological effects of CEACAM1.ResultsCEACAM1 plays a pivotal role in vascular homeostasis, particularly influencing the formation, maturation, and aging of blood vessels, as well as the endothelial barrier function. It supports endothelium-dependent vasodilation and nitric oxide formation, thus promoting vascular integrity and regulating blood pressure. Additionally, CEACAM1 is of emerging importance to vascular inflammation and its potential clinical consequences.ConclusionCEACAM1 is a crucial regulator of vascular homeostasis and inflammation with significant implications for cardiovascular health. Despite the lack of understanding of tissue-specific modulation and isoform-dependent mechanisms, CEACAM1 could be a promising therapeutic target for the prevention of cardiovascular disease in the future.
引用
收藏
页数:9
相关论文
共 71 条
[61]   CD66-DEPENDENT NEUTROPHIL ACTIVATION - A POSSIBLE MECHANISM FOR VASCULAR SELECTIN-MEDIATED REGULATION OF NEUTROPHIL ADHESION [J].
STOCKS, SC ;
KERR, MA ;
HASLETT, C ;
DRANSFIELD, I .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 58 (01) :40-48
[62]   NEUTROPHIL NCA-160 (CD66) IS THE MAJOR PROTEIN CARRIER OF SELECTIN BINDING CARBOHYDRATE GROUPS LEWIS(X) AND SIALYL LEWIS(X) [J].
STOCKS, SC ;
KERR, MA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 195 (01) :478-483
[63]   Single-cell transcriptomics uncover hub genes and cell-cell crosstalk in patients with hypertensive nephropathy [J].
Tang, Rong ;
Lin, Wei ;
Shen, Chanjuan ;
Hu, Xueling ;
Yu, Leilin ;
Meng, Ting ;
Zhang, Linlin ;
Eggenhuizen, Peter J. ;
Ooi, Joshua D. ;
Jin, Peng ;
Ding, Xiang ;
Xiao, Xiangcheng ;
Zhong, Yong .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2023, 125
[64]   Expression of newly identified secretory CEACAM1a isoforms in the intestinal epithelium [J].
Terahara, Kazutaka ;
Yoshida, Masato ;
Taguchi, Fumihiro ;
Igarashi, Osamu ;
Nochi, Tomonori ;
Gotoh, Yoshiyuki ;
Yamamoto, Takuya ;
Tsunetsugu-Yokota, Yasuko ;
Beauchemin, Nicole ;
Kiyono, Hiroshi .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 383 (03) :340-346
[65]   CEA-related cell adhesion molecule-1 is involved in angiogenic switch in prostate cancer [J].
Tilki, D. ;
Irmak, S. ;
Oliveira-Ferrer, L. ;
Hauschild, J. ;
Miethe, K. ;
Atakaya, H. ;
Hammerer, P. ;
Friedrich, M. G. ;
Schuch, G. ;
Galalae, R. ;
Stief, C. G. ;
Kilic, E. ;
Huland, H. ;
Ergun, S. .
ONCOGENE, 2006, 25 (36) :4965-4974
[66]   Loss of CEACAM1, a Tumor-Associated Factor, Attenuates Post-infarction Cardiac Remodeling by Inhibiting Apoptosis [J].
Wang, Yan ;
Chen, Yanmei ;
Yan, Yi ;
Li, Xinzhong ;
Chen, Guojun ;
He, Nvqin ;
Shen, Shuxin ;
Chen, Gangbin ;
Zhang, Chuanxi ;
Liao, Wangjun ;
Liao, Yulin ;
Bin, Jianping .
SCIENTIFIC REPORTS, 2016, 6
[67]   Homophilic adhesion of human CEACAM1 involves N-terminal domain interactions: structural analysis of the binding site [J].
Watt, SM ;
Teixeira, AM ;
Zhou, GQ ;
Doyonnas, R ;
Zhang, Y ;
Grunert, F ;
Blumberg, RS ;
Kuroki, M ;
Skubitz, KM ;
Bates, PA .
BLOOD, 2001, 98 (05) :1469-1479
[68]   Inhibition of cell invasion and migration by CEACAM1-4S in breast cancer [J].
Yang, Changcheng ;
Cao, Manlin ;
Liu, Yiwen ;
He, Yiqing ;
Yang, Cuixia ;
Du, Yan ;
Wang, Wenjuan ;
Zhang, Guoliang ;
Wu, Man ;
Zhou, Muqing ;
Gao, Feng .
ONCOLOGY LETTERS, 2017, 14 (04) :4758-4766
[69]   CEACAM1 (CD66a) promotes human monocyte survival via a phosphatidylinositol 3-kinase- and AKT-dependent pathway [J].
Yu, Qigui ;
Chow, Edith M. C. ;
Wong, Henry ;
Gu, Jenny ;
Mandelboim, Ofer ;
Gray-Owen, Scott D. ;
Ostrowski, Mario A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (51) :39179-39193
[70]   Loss of CEACAM1 in hepatocytes causes hepatic fibrosis [J].
Zaidi, Sobia ;
Asalla, Suman ;
Muturi, Harrison T. ;
Russo, Lucia ;
Abdolahipour, Raziyeh ;
Belew, Getachew Debas ;
Iglesias, Maria Benitez ;
Feraudo, Mary ;
Leon, Lensay ;
Kuo, Enoch ;
Liu, Xiuli ;
Kumarasamy, Sivarajan ;
Ghadieh, Hilda E. ;
Gatto-Weis, Cara ;
Zarrinpar, Ali ;
Duarte, Sergio ;
Najjar, Sonia M. .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2024, 54 (07)