The Role of Neuropilin-1 (NRP-1) in SARS-CoV-2 Infection: Review.
The Role of Neuropilin-1 (NRP-1) in SARS-CoV-2 Infection: Review.
复制标题
神经毛蛋白-1(NRP-1)在SARS-CoV-2感染中的作用:综述。
DOI:
10.3390/jcm10132772
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发表时间:
2021-06-24
影响因子:
3.9
通讯作者:
Mroczko B
中科院分区:
文献类型:
--
作者:
Gudowska-Sawczuk M;Mroczko B
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), discovered in 2019, is responsible for the global coronavirus disease 19 (COVID-19) pandemic. The main protein that interacts with the host cell receptor is the Spike-1 (S1) subunit of the coronavirus. This subunit binds with receptors present on the host cell membrane. It has been identified from several studies that neuropilin-1 (NRP-1) is one of the co-receptors for SARS-CoV-2 entry. Therefore, in this review, we focus on the significance of NRP-1 in SARS-CoV-2 infection. MEDLINE/PubMed database was used for a search of available literature. In the current review, we report that NRP-1 plays many important functions, including angiogenesis, neuronal development, and the regulation of immune responses. Additionally, the presence of this glycoprotein on the host cell membrane significantly augments the infection and spread of SARS-CoV-2. Literature data suggest that NRP-1 facilitates entry of the virus into the central nervous system through the olfactory epithelium of the nasal cavity. Moreover, published findings show that interfering with VEGF-A/NRP-1 using NRP-1 inhibitors may produce an analgesic effect. The review describes an association between NRP-1, SARS-CoV-2 and, inter alia, pathological changes in the retina. Based on the published findings, we suggest that NRP-1 is a very important mediator implicated in, inter alia, neurological manifestations of SARS-CoV-2 infection. Additionally, it appears that the use of NRP-1 inhibitors is a promising therapeutic strategy for the treatment of SARS-CoV-2 infection.
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DOI:
10.1126/science.abd3072
发表时间:
2020-11-13
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Daly JL;Simonetti B;Klein K;Chen KE;Williamson MK;Antón-Plágaro C;Shoemark DK;Simón-Gracia L;Bauer M;Hollandi R;Greber UF;Horvath P;Sessions RB;Helenius A;Hiscox JA;Teesalu T;Matthews DA;Davidson AD;Collins BM;Cullen PJ;Yamauchi Y
通讯作者:
Yamauchi Y
影响因子:
4.5
作者:
Mihaescu G;Chifiriuc MC;Iliescu C;Vrancianu CO;Ditu LM;Marutescu LG;Grigore R;Berteșteanu Ș;Constantin M;Gradisteanu Pircalabioru G
通讯作者:
Gradisteanu Pircalabioru G
影响因子:
39.3
作者:
Kyrou I;Randeva HS;Spandidos DA;Karteris E
通讯作者:
Karteris E
影响因子:
8.4
作者:
Amzat, Jimoh;Aminu, Kafayat;Danjibo, Maryann C.
通讯作者:
Danjibo, Maryann C.
影响因子:
3.4
作者:
Davies J;Randeva HS;Chatha K;Hall M;Spandidos DA;Karteris E;Kyrou I
通讯作者:
Kyrou I