It has been previously shown that intestinal proteases translocate into the circulation during hemorrhagic shock and contribute to proteolysis in distal organs. However, consequences of this phenomenon have not previously been investigated using high-throughput approaches. Here, a shotgun label-free quantitative proteomic approach was utilized to compare the peptidome of plasma samples from healthy and hemorrhagic shock rats to verify the possible role of uncontrolled proteolytic activity in shock. Plasma was collected from rats after hemorrhagic shock (HS) consisting of two-hour hypovolemia followed by two-hour reperfusion, and from healthy control (CTRL) rats. A new two-step enrichment method was applied to selectively extract peptides and low molecular weight proteins from plasma, and directly analyze these samples by tandem mass spectrometry. 126 circulating peptides were identified in CTRL and 295 in HS animals. 96 peptides were present in both conditions; of these, 57 increased and 30 decreased in shock. In total, 256 peptides were increased or present only in HS confirming a general increase in proteolytic activity in shock. Analysis of the proteases that potentially generated the identified peptides suggests that the larger relative contribution of to the proteolytic activity in shock is due to chymotryptic-like proteases. These results provide quantitative confirmation that extensive, system-wide proteolysis is part of the complex pathologic phenomena occurring in hemorrhagic shock.

Peptidomic Analysis of Rat Plasma: Proteolysis in Hemorrhagic Shock / F. Aletti, E. Maffioli, A. Negri, M.H. Santamaria, F.A. De Lano, E.B. Kistler, G.W. Schmid Schönbein, G. Tedeschi. - In: SHOCK. - ISSN 1073-2322. - 45:5(2016 May 01), pp. 540-554. [10.1097/SHK.0000000000000532]

Peptidomic Analysis of Rat Plasma: Proteolysis in Hemorrhagic Shock

E. Maffioli;A. Negri;G. Tedeschi
Ultimo
2016

Abstract

It has been previously shown that intestinal proteases translocate into the circulation during hemorrhagic shock and contribute to proteolysis in distal organs. However, consequences of this phenomenon have not previously been investigated using high-throughput approaches. Here, a shotgun label-free quantitative proteomic approach was utilized to compare the peptidome of plasma samples from healthy and hemorrhagic shock rats to verify the possible role of uncontrolled proteolytic activity in shock. Plasma was collected from rats after hemorrhagic shock (HS) consisting of two-hour hypovolemia followed by two-hour reperfusion, and from healthy control (CTRL) rats. A new two-step enrichment method was applied to selectively extract peptides and low molecular weight proteins from plasma, and directly analyze these samples by tandem mass spectrometry. 126 circulating peptides were identified in CTRL and 295 in HS animals. 96 peptides were present in both conditions; of these, 57 increased and 30 decreased in shock. In total, 256 peptides were increased or present only in HS confirming a general increase in proteolytic activity in shock. Analysis of the proteases that potentially generated the identified peptides suggests that the larger relative contribution of to the proteolytic activity in shock is due to chymotryptic-like proteases. These results provide quantitative confirmation that extensive, system-wide proteolysis is part of the complex pathologic phenomena occurring in hemorrhagic shock.
English
Hemorrhagic shock; mass spectrometry; matrix metalloproteases; peptidomics; proteolysis; serine-proteases;
Settore BIO/10 - Biochimica
Articolo
Esperti anonimi
Ricerca di base
Pubblicazione scientifica
1-mag-2016
6-nov-2016
Lippincott Williams and Wilkins
45
5
540
554
15
Pubblicato
Periodico con rilevanza internazionale
crossref
Aderisco
info:eu-repo/semantics/article
Peptidomic Analysis of Rat Plasma: Proteolysis in Hemorrhagic Shock / F. Aletti, E. Maffioli, A. Negri, M.H. Santamaria, F.A. De Lano, E.B. Kistler, G.W. Schmid Schönbein, G. Tedeschi. - In: SHOCK. - ISSN 1073-2322. - 45:5(2016 May 01), pp. 540-554. [10.1097/SHK.0000000000000532]
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Article (author)
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F. Aletti, E. Maffioli, A. Negri, M.H. Santamaria, F.A. De Lano, E.B. Kistler, G.W. Schmid Schönbein, G. Tedeschi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/357873
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