The Effect of Sepsis on the Erythrocyte

被引:129
作者
Bateman, Ryon M. [1 ]
Sharpe, Michael D. [2 ]
Singer, Mervyn [3 ,4 ]
Ellis, Christopher G. [1 ]
机构
[1] Univ Western Ontario, Dept Med Biophys, London, ON N6A 5C1, Canada
[2] Univ Western Ontario, Dept Anesthesia & Crit Care Western, London, ON N6A 5C1, Canada
[3] UCL, Div Med, Res Dept Clin Physiol, London WC1E 6BT, England
[4] UCL, Bloomsbury Inst Intens Care Med, London WC1E 6BT, England
关键词
sepsis; erythrocyte; rheology; morphology and microcirculation; RED-BLOOD-CELL; CRITICALLY-ILL PATIENTS; RAT SKELETAL-MUSCLE; IN-VIVO; LIPID-PEROXIDATION; DISTRIBUTION WIDTH; HYDROGEN-PEROXIDE; SEPTIC SHOCK; TYROSINE PHOSPHORYLATION; ANTIOXIDANT STATUS;
D O I
10.3390/ijms18091932
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sepsis induces a wide range of effects on the red blood cell (RBC). Some of the effects including altered metabolism and decreased 2,3-bisphosphoglycerate are preventable with appropriate treatment, whereas others, including decreased erythrocyte deformability and redistribution of membrane phospholipids, appear to be permanent, and factors in RBC clearance. Here, we review the effects of sepsis on the erythrocyte, including changes in RBC volume, metabolism and hemoglobin's affinity for oxygen, morphology, RBC deformability (an early indicator of sepsis), antioxidant status, intracellular Ca2+ homeostasis, membrane proteins, membrane phospholipid redistribution, clearance and RBC O-2-dependent adenosine triphosphate efflux (an RBC hypoxia signaling mechanism involved in microvascular autoregulation). We also consider the causes of these effects by host mediated oxidant stress and bacterial virulence factors. Additionally, we consider the altered erythrocyte microenvironment due to sepsis induced microvascular dysregulation and speculate on the possible effects of RBC autoxidation. In future, a better understanding of the mechanisms involved in sepsis induced erythrocyte pathophysiology and clearance may guide improved sepsis treatments. Evidence that small molecule antioxidants protect the erythrocyte from loss of deformability, and more importantly improve septic patient outcome suggest further research in this area is warranted. While not generally considered a critical factor in sepsis, erythrocytes (and especially a smaller subpopulation) appear to be highly susceptible to sepsis induced injury, provide an early warning signal of sepsis and are a factor in the microvascular dysfunction that has been associated with organ dysfunction.
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页数:23
相关论文
共 157 条
[1]   Effect of bacterial peptidoglycan on erythrocyte death and adhesion to endothelial cells [J].
Abed, Majed ;
Towhid, Syeda T. ;
Pakladok, Tatsiana ;
Alesutan, Ioana ;
Goetz, Friedrich ;
Gulbins, Erich ;
Lang, Florian .
INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2013, 303 (04) :182-189
[2]   Sphingomyelinase-induced adhesion of eryptotic erythrocytes to endothelial cells [J].
Abed, Majed ;
Towhid, Syeda T. ;
Mia, Sobuj ;
Pakladok, Tatsiana ;
Alesutan, Ioana ;
Borst, Oliver ;
Gawaz, Meinrad ;
Gulbins, Erich ;
Lang, Florian .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2012, 303 (09) :C991-C999
[3]   ERYTHROCYTE CATALASE - A SOMATIC OXIDANT DEFENSE [J].
AGAR, NS ;
SADRZADEH, SMH ;
HALLAWAY, PE ;
EATON, JW .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (01) :319-321
[4]  
de Oliveira YPA, 2017, BRAZ J INFECT DIS, V21, P19
[5]  
[Anonymous], 2016, RES, DOI DOI 10.1080/10715762.2016.124199527677384
[6]   Phagocytes and oxidative stress [J].
Babior, BM .
AMERICAN JOURNAL OF MEDICINE, 2000, 109 (01) :33-44
[7]   Production of superoxide from hemoglobin-bound oxygen under hypoxic conditions [J].
Balagopalakrishna, C ;
Manoharan, PT ;
Abugo, OO ;
Rifkind, JM .
BIOCHEMISTRY, 1996, 35 (20) :6393-6398
[8]   Superoxide produced in the heme pocket of the β-chain of hemoglobin reacts with the β-93 cysteine to produce a thiyl radical [J].
Balagopalakrishna, C ;
Abugo, OO ;
Horsky, J ;
Manoharan, PT ;
Nagababu, E ;
Rifkind, JM .
BIOCHEMISTRY, 1998, 37 (38) :13194-13202
[9]   Deoxygenation and elevation of intracellular magnesium induce tyrosine phosphorylation of band 3 in human erythrocytes [J].
Barbul, A ;
Zipser, Y ;
Nachles, A ;
Korenstein, R .
FEBS LETTERS, 1999, 455 (1-2) :87-91
[10]   Red blood cell deformability in sepsis [J].
Baskurt, OK ;
Gelmont, D ;
Meiselman, HJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (02) :421-427