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pmid:32785189

Insights into Biomechanical and Proteomic Characteristics of Small Diameter Vascular Grafts Utilizing the Human Umbilical Artery.

Panagiotis Mallis · Dimitrios P Sokolis · Manousos Makridakis · Jerome Zoidakis · Athanasios D Velentzas · Michalis Katsimpoulas · Antonia Vlahou · Alkiviadis Kostakis · Catherine Stavropoulos-Giokas · Efstathios Michalopoulos

Biomedicines · 2020 doi:10.3390/biomedicines8080280

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Experiment

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pmid:32785189
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2026-11-01T15:41:07Z
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paper object · 10 fields
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title
Insights into Biomechanical and Proteomic Characteristics of Small Diameter Vascular Grafts Utilizing the Human Umbilical Artery.
doi
10.3390/biomedicines8080280
pmid
32785189
authors array · 10 items
[0]
Panagiotis Mallis
[1]
Dimitrios P Sokolis
[2]
Manousos Makridakis
[3]
Jerome Zoidakis
[4]
Athanasios D Velentzas
[5]
Michalis Katsimpoulas
[6]
Antonia Vlahou
[7]
Alkiviadis Kostakis
[8]
Catherine Stavropoulos-Giokas
[9]
Efstathios Michalopoulos
journal
Biomedicines
year
2020
abstract
The gold standard vascular substitutes, used in cardiovascular surgery, are the Dacron or expanded polytetrafluoroethylene (ePTFE)-derived grafts. However, major adverse reactions accompany their use. For this purpose, decellularized human umbilical arteries (hUAs) may be proven as a significant source for the development of small diameter conduits. The aim of this study was the evaluation of a decellularization protocol in hUAs. To study the effect of the decellularization to the hUAs, histological analysis was performed. Then, native and decellularized hUAs were biochemically and biomechanically evaluated. Finally, broad proteomic analysis was applied. Histological analysis revealed the successful decellularization of the hUAs. Furthermore, a great amount of DNA was removed from the decellularized hUAs. Biomechanical analysis revealed statistically significant differences in longitudinal direction only in maximum stress (p < 0.013) and strain (p < 0.001). On the contrary, all parameters tested for circumferential direction exhibited significant differences (p < 0.05). Proteomic analysis showed the preservation of the extracellular matrix and cytoskeletal proteins in both groups. Proteomic data are available via ProteomeXchange with identifier PXD020187. The above results indicated that hUAs were efficiently decellularized. The tissue function properties of these conduits were well retained, making them ideal candidates for the development of small diameter vascular grafts.
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Collagen, sGAG, and DNA quantification data were compared using the Mann-Whitney test. Statistical significance was considered when the p-value was less than 0.05. Indicated values were the mean ± standard deviation. The unpaired Student’s t-test was used for comparisons of the biomechanical parameters between decellularized and native arteries, while comparisons between directions were assessed with the paired t-test. The Pearson correlation coefficient r was used for identifying associations of the biomechanical parameters with gestational age, infant’s weight, and arterial caliber, i.e., wall thickness and diameter. The effect of infant’s gender on the biomechanical properties was assessed with the unpaired t-test.
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sections[15] "2.13. Statistical Analysis" paragraph 2
quote
Collagen, sGAG, and DNA quantification data were compared using the Mann-Whitney test. Statistical significance was considered when the p-value was less than 0.05. Indicated values were the mean ± standard deviation. The unpaired Student’s t-test was used for comparisons of the biomechanical parameters between decellularized and native arteries, while comparisons between directions were assessed with the paired t-test. The Pearson correlation coefficient r was used for identifying associations of the biomechanical parameters with gestational age, infant’s weight, and arterial caliber, i.e., wall thickness and diameter. The effect of infant’s gender on the biomechanical properties was assessed with the unpaired t-test.
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The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD020187.
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sections[24] "Appendix A" paragraph 2
quote
The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD020187.
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Proteomic evaluation of decellularized human umbilical artery
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List of representative identified proteins in native human umbilical arteries (hUAs).
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3.4. Proteomic Evaluation of hUAs
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Table 1
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List of representative identified proteins in native human umbilical arteries (hUAs).
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[0] array · 5 items
[0]
No.
[1]
Accession Number
[2]
Description
[3]
Score
[4]
% Sequence Coverage
[1] array · 5 items
[0]
1
[1]
P62736
[2]
Actin, aortic smooth muscle
[3]
2310
[4]
57
[2] array · 5 items
[0]
2
[1]
P21333
[2]
Filamin-A
[3]
1670
[4]
50
[3] array · 5 items
[0]
3
[1]
P12111
[2]
Collagen alpha-3 (VI)
[3]
1106
[4]
35
[4] array · 5 items
[0]
4
[1]
P60709
[2]
Actin, cytoplasmic 1
[3]
1042
[4]
53
[5] array · 5 items
[0]
5
[1]
P35749
[2]
Myosin-11
[3]
877
[4]
34
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[0]
6
[1]
A5A3E0
[2]
POTE ankyrin domain family member F
[3]
816
[4]
6
[7] array · 5 items
[0]
7
[1]
P98160
[2]
Basement membrane-specific heparan sulfate proteoglycan core protein
[3]
632
[4]
33
[8] array · 5 items
[0]
8
[1]
P02751
[2]
Fibronectin
[3]
534
[4]
40
[9] array · 5 items
[0]
9
[1]
P17661
[2]
Desmin
[3]
450
[4]
47
[10] array · 5 items
[0]
10
[1]
P12814
[2]
Alpha-actinin-1
[3]
444
[4]
51
[11] array · 5 items
[0]
11
[1]
Q9Y490
[2]
Talin-1
[3]
436
[4]
37
[12] array · 5 items
[0]
12
[1]
O43707
[2]
Alpha-actinin-4
[3]
396
[4]
59
[13] array · 5 items
[0]
13
[1]
P35579
[2]
Myosin-9
[3]
362
[4]
29
[14] array · 5 items
[0]
14
[1]
P09493
[2]
Tropomyosin alpha-1 chain
[3]
338
[4]
24
[15] array · 5 items
[0]
15
[1]
P08670
[2]
Vimentin
[3]
331
[4]
34
[16] array · 5 items
[0]
16
[1]
Q14315
[2]
Filamin-C
[3]
330
[4]
32
[17] array · 5 items
[0]
17
[1]
P67936
[2]
Tropomyosin alpha-4 chain
[3]
319
[4]
17
[18] array · 5 items
[0]
18
[1]
P12109
[2]
Collagen alpha-1 (VI) chain
[3]
318
[4]
33
[19] array · 5 items
[0]
19
[1]
P18206
[2]
Vinculin OS = Homo sapiens
[3]
316
[4]
36
[20] array · 5 items
[0]
20
[1]
P07951
[2]
Tropomyosin beta chain
[3]
307
[4]
17
[21] array · 5 items
[0]
21
[1]
Q09666
[2]
Neuroblast differentiation-associated protein AHNAK
[3]
293
[4]
26
[22] array · 5 items
[0]
22
[1]
P12110
[2]
Collagen alpha-2 (VI) chain
[3]
260
[4]
19
[23] array · 5 items
[0]
23
[1]
P69905
[2]
Hemoglobin subunit alpha
[3]
257
[4]
77
[24] array · 5 items
[0]
24
[1]
Q05707
[2]
Collagen alpha-1 (XIV) chain
[3]
244
[4]
28
[25] array · 5 items
[0]
25
[1]
P46940
[2]
Ras GTPase-activating-like protein IQGAP1
[3]
233
[4]
41
[26] array · 5 items
[0]
26
[1]
O15061
[2]
Synemin
[3]
232
[4]
39
[27] array · 5 items
[0]
27
[1]
P35580
[2]
Myosin-10
[3]
216
[4]
21
[28] array · 5 items
[0]
28
[1]
Q15149
[2]
Plectin
[3]
214
[4]
16
[29] array · 5 items
[0]
29
[1]
Q01995
[2]
Transgelin
[3]
206
[4]
53
[30] array · 5 items
[0]
30
[1]
P02768
[2]
Serum albumin
[3]
198
[4]
37
[31] array · 5 items
[0]
31
[1]
P01023
[2]
Alpha-2-macroglobulin
[3]
188
[4]
41
[32] array · 5 items
[0]
32
[1]
P04406
[2]
Glyceraldehyde-3-phosphate dehydrogenase
[3]
186
[4]
61
[33] array · 5 items
[0]
33
[1]
Q16363
[2]
Laminin subunit alpha-4
[3]
173
[4]
17
[34] array · 5 items
[0]
34
[1]
P21980
[2]
Protein-glutamine gamma-glutamyltransferase 2
[3]
172
[4]
42
[35] array · 5 items
[0]
35
[1]
Q14204
[2]
Cytoplasmic dynein 1 heavy chain 1
[3]
171
[4]
14
[36] array · 5 items
[0]
36
[1]
Q71U36
[2]
Tubulin alpha-1A chain
[3]
166
[4]
50
[37] array · 5 items
[0]
37
[1]
P07437
[2]
Tubulin beta chain
[3]
160
[4]
64
[38] array · 5 items
[0]
38
[1]
P51911
[2]
Calponin-1
[3]
150
[4]
54
[39] array · 5 items
[0]
39
[1]
P20774
[2]
Mimecan
[3]
149
[4]
30
[40] array · 5 items
[0]
40
[1]
P21810
[2]
Biglycan
[3]
146
[4]
32
[41] array · 5 items
[0]
41
[1]
Q15582
[2]
Transforming growth factor-beta-induced protein ig-h3
[3]
145
[4]
34
[42] array · 5 items
[0]
42
[1]
Q99715
[2]
Collagen alpha-1 (XII) chain
[3]
142
[4]
19
[43] array · 5 items
[0]
43
[1]
Q00610
[2]
Clathrin heavy chain 1
[3]
141
[4]
23
[44] array · 5 items
[0]
44
[1]
P54652
[2]
Heat shock-related 70 kDa protein 2
[3]
140
[4]
43
[45] array · 5 items
[0]
45
[1]
P06733
[2]
Alpha-enolase
[3]
140
[4]
46
[46] array · 5 items
[0]
46
[1]
P68371
[2]
Tubulin beta-4B chain
[3]
138
[4]
60
[47] array · 5 items
[0]
47
[1]
P12277
[2]
Creatine kinase B-type
[3]
136
[4]
68
[48] array · 5 items
[0]
48
[1]
P14543
[2]
Nidogen-1
[3]
135
[4]
35
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[0]
49
[1]
P06396
[2]
Gelsolin
[3]
135
[4]
27
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[0]
50
[1]
P08133
[2]
Annexin A6 OS
[3]
133
[4]
39
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section[20]/table-wrap[1]#biomedicines-08-00280-t001
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List of representative identified proteins in decellularized hUAs.
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PMC7460081
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3.4. Proteomic Evaluation of hUAs
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5
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Table 2
caption
List of representative identified proteins in decellularized hUAs.
rows array · 51 items
[0] array · 5 items
[0]
No.
[1]
Accession Number
[2]
Description
[3]
Score
[4]
% Sequence Coverage
[1] array · 5 items
[0]
1
[1]
P62736
[2]
Actin, aortic smooth muscle
[3]
5114
[4]
63
[2] array · 5 items
[0]
2
[1]
P21333
[2]
Filamin-A
[3]
1644
[4]
48
[3] array · 5 items
[0]
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[1]
P60709
[2]
Actin, cytoplasmic 1
[3]
1355
[4]
57
[4] array · 5 items
[0]
4
[1]
P12111
[2]
Collagen alpha-3 (VI) chain
[3]
1284
[4]
37
[5] array · 5 items
[0]
5
[1]
Q562R1
[2]
Beta-actin-like protein 2
[3]
970
[4]
18
[6] array · 5 items
[0]
6
[1]
P98160
[2]
Basement membrane-specific heparan sulfate proteoglycan core protein
[3]
891
[4]
40
[7] array · 5 items
[0]
7
[1]
A5A3E0
[2]
POTE ankyrin domain family member F
[3]
873
[4]
7
[8] array · 5 items
[0]
8
[1]
P35749
[2]
Myosin-11
[3]
800
[4]
32
[9] array · 5 items
[0]
9
[1]
P02751
[2]
Fibronectin
[3]
525
[4]
38
[10] array · 5 items
[0]
10
[1]
P12109
[2]
Collagen alpha-1 (VI) chain
[3]
477
[4]
36
[11] array · 5 items
[0]
11
[1]
P17661
[2]
Desmin
[3]
452
[4]
51
[12] array · 5 items
[0]
12
[1]
P35579
[2]
Myosin-9
[3]
397
[4]
29
[13] array · 5 items
[0]
13
[1]
Q14315
[2]
Filamin-C
[3]
366
[4]
36
[14] array · 5 items
[0]
14
[1]
P08670
[2]
Vimentin
[3]
338
[4]
33
[15] array · 5 items
[0]
15
[1]
Q9Y490
[2]
Talin-1
[3]
314
[4]
39
[16] array · 5 items
[0]
16
[1]
P35580
[2]
Myosin-10
[3]
302
[4]
26
[17] array · 5 items
[0]
17
[1]
P12110
[2]
Collagen alpha-2 (VI) chain
[3]
291
[4]
22
[18] array · 5 items
[0]
18
[1]
Q14204
[2]
Cytoplasmic dynein 1 heavy chain 1
[3]
262
[4]
22
[19] array · 5 items
[0]
19
[1]
P46940
[2]
Ras GTPase-activating-like protein IQGAP1
[3]
242
[4]
43
[20] array · 5 items
[0]
20
[1]
Q15149
[2]
Plectin
[3]
238
[4]
19
[21] array · 5 items
[0]
21
[1]
Q71U36
[2]
Tubulin alpha-1A chain
[3]
219
[4]
60
[22] array · 5 items
[0]
22
[1]
P21980
[2]
Protein-glutamine gamma-glutamyltransferase 2
[3]
200
[4]
47
[23] array · 5 items
[0]
23
[1]
O15061
[2]
Synemin
[3]
197
[4]
37
[24] array · 5 items
[0]
24
[1]
P07437
[2]
Tubulin beta chain
[3]
190
[4]
67
[25] array · 5 items
[0]
25
[1]
P68371
[2]
Tubulin beta-4B chain
[3]
179
[4]
64
[26] array · 5 items
[0]
26
[1]
O15230
[2]
Laminin subunit alpha-5
[3]
176
[4]
14
[27] array · 5 items
[0]
27
[1]
Q15063
[2]
Periostin
[3]
174
[4]
42
[28] array · 5 items
[0]
28
[1]
P20774
[2]
Mimecan
[3]
170
[4]
30
[29] array · 5 items
[0]
29
[1]
Q13885
[2]
Tubulin beta-2A chain
[3]
161
[4]
64
[30] array · 5 items
[0]
30
[1]
P68366
[2]
Tubulin alpha-4A chain
[3]
159
[4]
38
[31] array · 5 items
[0]
31
[1]
P68104
[2]
Elongation factor 1-alpha 1
[3]
159
[4]
46
[32] array · 5 items
[0]
32
[1]
Q16363
[2]
Laminin subunit alpha-4
[3]
155
[4]
16
[33] array · 5 items
[0]
33
[1]
P12814
[2]
Alpha-actinin-1
[3]
154
[4]
37
[34] array · 5 items
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34
[1]
Q00610
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Clathrin heavy chain 1
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149
[4]
27
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35
[1]
P21810
[2]
Biglycan
[3]
146
[4]
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[0]
36
[1]
Q99715
[2]
Collagen alpha-1 (XII) chain
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145
[4]
18
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[0]
37
[1]
P04406
[2]
Glyceraldehyde-3-phosphate dehydrogenase
[3]
145
[4]
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[0]
38
[1]
O43707
[2]
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[3]
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[4]
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[1]
P55268
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[4]
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[1]
P39060
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14
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[1]
P14543
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[1]
P06733
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135
[4]
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[0]
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[1]
P04792
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131
[4]
62
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[0]
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[1]
Q05707
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[4]
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[0]
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[1]
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[4]
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[1]
P51911
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128
[4]
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[47] array · 5 items
[0]
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[1]
O75083
[2]
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[3]
125
[4]
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[48] array · 5 items
[0]
48
[1]
Q9NZN4
[2]
EH domain-containing protein 2
[3]
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[4]
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49
[1]
P11532
[2]
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[3]
115
[4]
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[0]
50
[1]
P69905
[2]
Hemoglobin subunit alpha
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115
[4]
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Classification of the identified proteins in native and decellularized hUAs. Protein classification based on their molecular function was performed using the Panther analysis tool.
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Classification of the identified proteins in native and decellularized hUAs. Protein classification based on their molecular function was performed using the Panther analysis tool.
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Collagen, sGAG, and DNA quantification data were compared using the Mann-Whitney test. Statistical significance was considered when the p-value was less than 0.05. Indicated values were the mean ± standard deviation. The unpaired Student’s t-test was used for comparisons of the biomechanical parameters between decellularized and native arteries, while comparisons between directions were assessed with the paired t-test. The Pearson correlation coefficient r was used for identifying associations of the biomechanical parameters with gestational age, infant’s weight, and arterial caliber, i.e., wall thickness and diameter. The effect of infant’s gender on the biomechanical properties was assessed with the unpaired t-test.
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The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD020187.
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Collagen, sGAG, and DNA quantification data were compared using the Mann-Whitney test. Statistical significance was considered when the p-value was less than 0.05. Indicated values were the mean ± standard deviation. The unpaired Student’s t-test was used for comparisons of the biomechanical parameters between decellularized and native arteries, while comparisons between directions were assessed with the paired t-test. The Pearson correlation coefficient r was used for identifying associations of the biomechanical parameters with gestational age, infant’s weight, and arterial caliber, i.e., wall thickness and diameter. The effect of infant’s gender on the biomechanical properties was assessed with the unpaired t-test.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32785189", "kind": "science-record", "revision": 8, "content_hash": "sha256:4532ce6d6aabcdcb9c2d6a8f6dbce0007ff0bfb9875bc04388477cdc6f513a70", "created_at": "2026-11-01T15:41:07Z", "updated_at": "2026-11-01T22:45:11Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Insights into Biomechanical and Proteomic Characteristics of Small Diameter Vascular Grafts Utilizing the Human Umbilical Artery.", "doi": "10.3390/biomedicines8080280", "pmid": "32785189", "authors": ["Panagiotis Mallis", "Dimitrios P Sokolis", "Manousos Makridakis", "Jerome Zoidakis", "Athanasios D Velentzas", "Michalis Katsimpoulas", "Antonia Vlahou", "Alkiviadis Kostakis", "Catherine Stavropoulos-Giokas", "Efstathios Michalopoulos"], "journal": "Biomedicines", "year": 2020, "abstract": "The gold standard vascular substitutes, used in cardiovascular surgery, are the Dacron or expanded polytetrafluoroethylene (ePTFE)-derived grafts. However, major adverse reactions accompany their use. For this purpose, decellularized human umbilical arteries (hUAs) may be proven as a significant source for the development of small diameter conduits. The aim of this study was the evaluation of a decellularization protocol in hUAs. To study the effect of the decellularization to the hUAs, histological analysis was performed. Then, native and decellularized hUAs were biochemically and biomechanically evaluated. Finally, broad proteomic analysis was applied. Histological analysis revealed the successful decellularization of the hUAs. Furthermore, a great amount of DNA was removed from the decellularized hUAs. Biomechanical analysis revealed statistically significant differences in longitudinal direction only in maximum stress (p < 0.013) and strain (p < 0.001). On the contrary, all parameters tested for circumferential direction exhibited significant differences (p < 0.05). Proteomic analysis showed the preservation of the extracellular matrix and cytoskeletal proteins in both groups. Proteomic data are available via ProteomeXchange with identifier PXD020187. The above results indicated that hUAs were efficiently decellularized. The tissue function properties of these conduits were well retained, making them ideal candidates for the development of small diameter vascular grafts.", "claims": [{"id": "claim-method", "statement": "Collagen, sGAG, and DNA quantification data were compared using the Mann-Whitney test. Statistical significance was considered when the p-value was less than 0.05. Indicated values were the mean ± standard deviation. The unpaired Student’s t-test was used for comparisons of the biomechanical parameters between decellularized and native arteries, while comparisons between directions were assessed with the paired t-test. 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