Catestatin: Antimicrobial Functions and Potential Therapeutics.
Catestatin: Antimicrobial Functions and Potential Therapeutics.
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catestatin:抗菌功能和潜在的治疗剂。
DOI:
10.3390/pharmaceutics15051550
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发表时间:
2023-05-20
期刊:
影响因子:
5.4
通讯作者:
Mahata SK
中科院分区:
文献类型:
--
作者:
Jati S;Mahata S;Das S;Chatterjee S;Mahata SK
The rapid increase in drug-resistant and multidrug-resistant infections poses a serious challenge to antimicrobial therapies, and has created a global health crisis. Since antimicrobial peptides (AMPs) have escaped bacterial resistance throughout evolution, AMPs are a category of potential alternatives for antibiotic-resistant “superbugs”. The Chromogranin A (CgA)-derived peptide Catestatin (CST: hCgA352–372; bCgA344–364) was initially identified in 1997 as an acute nicotinic-cholinergic antagonist. Subsequently, CST was established as a pleiotropic hormone. In 2005, it was reported that N-terminal 15 amino acids of bovine CST (bCST1–15 aka cateslytin) exert antibacterial, antifungal, and antiyeast effects without showing any hemolytic effects. In 2017, D-bCST1–15 (where L-amino acids were changed to D-amino acids) was shown to exert very effective antimicrobial effects against various bacterial strains. Beyond antimicrobial effects, D-bCST1–15 potentiated (additive/synergistic) antibacterial effects of cefotaxime, amoxicillin, and methicillin. Furthermore, D-bCST1–15 neither triggered bacterial resistance nor elicited cytokine release. The present review will highlight the antimicrobial effects of CST, bCST1–15 (aka cateslytin), D-bCST1–15, and human variants of CST (Gly364Ser-CST and Pro370Leu-CST); evolutionary conservation of CST in mammals; and their potential as a therapy for antibiotic-resistant “superbugs”.
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影响因子:
3.7
作者:
Zhang D;Shooshtarizadeh P;Laventie BJ;Colin DA;Chich JF;Vidic J;de Barry J;Chasserot-Golaz S;Delalande F;Van Dorsselaer A;Schneider F;Helle K;Aunis D;Prévost G;Metz-Boutigue MH
通讯作者:
Metz-Boutigue MH
影响因子:
4.5
作者:
Corb Aron RA;Abid A;Vesa CM;Nechifor AC;Behl T;Ghitea TC;Munteanu MA;Fratila O;Andronie-Cioara FL;Toma MM;Bungau S
通讯作者:
Bungau S
DOI:
10.1152/ajpgi.00346.2017
发表时间:
2018-07-01
影响因子:
4.5
作者:
Christiansen, Charlotte Bayer;Gabe, Maria Buur Nordskov;Holst, Jens Juul
通讯作者:
Holst, Jens Juul
影响因子:
4.8
作者:
Biswas, Nilima;Rodriguez-Flores, Juan L.;Mahata, Sushil K.
通讯作者:
Mahata, Sushil K.
DOI:
10.1073/pnas.91.20.9297
发表时间:
1994-09-27
影响因子:
11.1
作者:
BROCCHIERI, L;KARLIN, S
通讯作者:
KARLIN, S