Use of connexin channel inhibitors to protect grafts

Patent metadata

Field	Value
Publication number	US-9485983-B2
Application number	US-201314650553-A
Country	US
Kind code	B2
Filing date	Dec 10, 2013
Priority date	Dec 19, 2012
Publication date	Nov 8, 2016
Grant date	Nov 8, 2016

Abstract

This disclosure relates to methods to protect grafts against cell death due to preservation of the grafts prior to transplanting these grafts into patients. In particular, this disclosure discloses that connexin channel inhibitors can be used to protect against cell death associated with preservation and temporary storage of cells, tissues and organs. Preservation includes any procedure that involves a lowering of the temperature below the normal body temperature, including hypothermia (cold storage), cryopreservation and vitrification. Grafts that are protected according to this disclosure have an improved biological function.

First claim

The invention claimed is:

1. A method of protecting a graft, the method comprising:
utilizing a connexin channel inhibitor to protect the graft against cell death due to preservation of the graft prior to transplanting the graft into an animal or human patient.

2. The method according to claim 1 , wherein said preservation includes cold storage, cryopreservation or vitrification, followed by thawing and/or washing of the graft.

3. The method according to claim 1 , wherein said connexin channel inhibitor is able to inhibit both gap junctions and hemichannels.

4. The method according to claim 3 , wherein said connexin channel inhibitor is selected from the group consisting of Gap26, Gap27, any combination of Gap26 and Gap27, and Gap26 and/or Gap27 combined with any of the following substances: antibodies directed against connexins, glycyrrhetinic acid, carbenoxolone, heptanol, octanol, halothane, arachidonic acid, oleic acid, oleamide, anandamide, flufenamic acid, niflumic acid, meclofenamic acid, 5-nitro-2-(3-phenyl-propylamino)benzoic acid (NPPB), disodium 4,4′-diisothiocyanatostilbene-2,2′-disulfonate (DIDS), quinine, quinidine, mefloquine, 2-aminoethoxydiphenyl borate (2-APB), spermine, spermidine, triphenylmethanes, triphenylethanes, triarylmethanes, cyclodextrins, the specific connexin hemichannel inhibitors Gap19 and/or Gap24, and the pannexin channel inhibitors 10 Panx1 peptide, probenecid, disodium 4-acetamido-4′-isothiocyanato-stilben-2,2′-disulfonate (SITS) and/or (indanyloxyacetic acid) IAA-94.

5. The method according to claim 4 , wherein Gap27 is the connexin mimetic inhibitor and has the consensus amino acid sequence X 1 X 2 PTEKX 3 X 4 FX 5 X 6 (SEQ ID NO:1), wherein X 1 is S or A, X 2 is R or K, X 3 is T, N or K, X 4 is I, V or L, X 5 is I, T, L or M and X 6 is I, V, L or Y, or a shortened version of Gap27, wherein the amino acids X 4 FX 5 X 6 or FX 5 X 6 or X 5 X 6 or X 6 are deleted and/or, wherein Gap26 is the connexin mimetic peptide having the consensus amino acid sequence X 1 CX 2 DX 3 X 4 X 5 PX 6 SX 7 X 8 R (SEQ ID NO:3), wherein X 1 is V, A or I, X 2 is Y or F, X 3 is K, Q, A, E, H, R, N or D, X 4 is S, A, F or Y, X 5 is F or A, X 6 is I, V or L, X 7 is H, N or L and X 8 is V, I or R, and/or, wherein said Gap19 is the connexin mimetic peptides having the sequence KQIEIKKFK (SEQ ID NO:4), and/or, wherein said Gap24 is the connexin mimetic peptides having the sequence GHGDPLHLEEVKC (SEQ ID NO:5), and/or wherein said 10 Panx1 peptide is the pannexin mimetic peptide having the amino acid sequence WRQAAFVDSY (SEQ ID NO:6).

6. The method according to claim 5 , wherein Gap27 is SRPTEKTIFII (SEQ ID NO:2).

7. The method according to claim 4 , wherein Gap19, Gap24, or, Gap19 and Gap24 are coupled to a cell internalization sequence.

8. The method according to claim 7 , wherein said internalization sequence is YGRKKRRQRRR (SEQ ID NO:7) or RQPKIWFPNRRKPWKK (SEQ ID NO:8).

9. The method according to claim 1 , wherein the graft is selected from the group consisting of oocyte, hepatocyte, stem cell, vascular graft, heart and uterus.

10. The method according to claim 9 , wherein said vascular graft is a human artery or vein.

11. The method according to claim 10 , wherein the vascular graft is selected from the group consisting of aorta, femoral artery, iliac artery, tibial, internal thoracic artery, saphenous vein, and iliac vein.

12. An in vitro method to protect grafts against cell death due to preservation of said grafts, the method comprising:
a) obtaining a graft from a donor,
b) adding a protective amount of connexin channel inhibitor to a solution suitable to preserve a graft,
c) placing said graft into said solution containing said connexin channel inhibitor, and
d) preserving said graft embedded in said solution containing said connexin channel inhibitor.

13. The in vitro method according to claim 12 , wherein said preservation includes cold storage/hypothermia, cryopreservation or vitrification, followed by thawing and washing said graft.

14. The in vitro method according to claim 13 , wherein said connexin channel inhibitor is separately added to a solution suitable to wash said previously cryopreserved and thawed graft.

15. The in vitro method according to claim 14 , wherein said solution suitable to cryopreserve grafts comprises Hank's Buffered Salt Solution (HBSS), 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid buffer (HEPES buffer) and dimethylsulfoxide (DMSO) and wherein said solution suitable to wash previously cryopreserved and thawed grafts comprises HBSS and HEPES buffer.

16. The method according to claim 1 that improves the biological function of the graft compared to the biological function of a graft that was not so protected.

17. The method according to claim 3 , wherein the connexin mimetic inhibitor is Gap27, which comprises X 1 X 2 PTEKX 3 X 4 FX 5 X 6 (SEQ ID NO:1), wherein
X 1 is S or A,
X 2 is R or K,
X 3 is T, N or K,
X 4 is I, V or L,
X 5 is I, T, L or M, and
X 6 is I, V, L or Y.

18. The method according to claim 3 , wherein the connexin mimetic inhibitor comprises X 1 X 2 PTEKX 3 X 4 (amino acids 1 through 8 of SEQ ID NO:1) or X 1 X 2 PTEKX 3 (amino acids 1 through 7 of SEQ ID NO:1), wherein
X 1 is S or A,
X 2 is R or K,
X 3 is T, N or K, and
X 4 is I, V or L.

19. The method according to claim 3 , wherein the connexin mimetic inhibitor is Gap26, which comprises X 1 CX 2 DX 3 X 4 X 5 PX 6 SX 7 X 8 R (SEQ ID NO:3), wherein
X 1 is V, A or I,
X 2 is Y or F,
X 3 is K, Q, A, E, H, R, N or D,
X 4 is S, A, F or Y,
X 5 is F or A,
X 6 is I, V or L,
X 7 is H, N or L, and
X 8 is V, I or R.

20. The method according to claim 3 , wherein the connexin mimetic inhibitor is Gap19, which comprises KQIEIKKFK (SEQ ID NO:4).

21. The method according to claim 3 , wherein the connexin mimetic inhibitor is Gap24, which comprises GHGDPLHLEEVKC (SEQ ID NO:5).

22. The method according to claim 4 , wherein 10 Panx1 peptide is the pannexin mimetic peptide, which comprises WRQAAFVDSY (SEQ ID NO:6).

Assignees

• Univ Gent

Inventors

• Leybaert Luc

Classifications

• A01N1/126

  Physiologically active agents, e.g. antioxidants or nutrients · CPC title

• A01N1/125 Primary

  Freeze protecting agents, e.g. cryoprotectants or osmolarity regulators · CPC title

• A01N1/0226

  Human Necessities · mapped topic

• A01N1/0221 Primary

  Human Necessities · mapped topic