marker (%) normal epcs mean ± sm (%) mmd epcs mean ± sm (%) cd3426.9 ± 11.531.0 ± 6.8 kdr27.3 ±...

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Marker (%) Normal EPCs Mean ± SM (%) MMD EPCs Mean ± SM (%) CD34 26.9 ± 11.5 31.0 ± 6.8 KDR 27.3 ± 5.52 22.4 ± 8.90 CD133 24.5 ± 4.64 12.6 ± 3.93 CD31 99.0 ± 0.9 98.8 ± 0.5 CD45 0.42 ± 1.23 1.53 ± 3.12 CD34 KDR CD133 CD31 B (Scale bar : 50 μm) CD31 vWF C D (Scale bar : 100 μm) Dil-Ac-LDL uptake Supplemental Figure I Normal MMD (Scale bar : 100 μm) A 21 days 28 days 35 days 7 days CD45 Normal MMD 0 10 20 30 40 50 Number of colonies (/well) ***

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Page 1: Marker (%) Normal EPCs Mean ± SM (%) MMD EPCs Mean ± SM (%) CD3426.9 ± 11.531.0 ± 6.8 KDR27.3 ± 5.5222.4 ± 8.90 CD13324.5 ± 4.6412.6 ± 3.93 CD3199.0 ±

Marker (%)Normal EPCs

Mean ± SM (%)

MMD EPCs Mean

± SM (%)

CD34 26.9 ± 11.5 31.0 ± 6.8

KDR 27.3 ± 5.52 22.4 ± 8.90

CD133 24.5 ± 4.64 12.6 ± 3.93

CD31 99.0 ± 0.9 98.8 ± 0.5

CD45 0.42 ± 1.23 1.53 ± 3.12

CD34 KDR CD133 CD31B

(Scale bar : 50 μm)

CD31 vWF

C D

(Scale bar : 100 μm)

Dil-Ac-LDL uptake

Supplemental Figure I

Normal MMD

(Scale bar : 100 μm)

A 21 days

28 days 35 days

7 days CD45

Normal MMD0

10

20

30

40

50

Nu

mb

er o

f co

lon

ies

(/w

ell)

***

Page 2: Marker (%) Normal EPCs Mean ± SM (%) MMD EPCs Mean ± SM (%) CD3426.9 ± 11.531.0 ± 6.8 KDR27.3 ± 5.5222.4 ± 8.90 CD13324.5 ± 4.6412.6 ± 3.93 CD3199.0 ±

β-actin

RALDH2

-

(-)con50 nM

siRNA(A)

50 nM

siRNA(B)

50 nM

(-) control siRNA

Non treated 10 nM

30 nM 50 nM

A B

C D

RALDH2 siRNA (A) (nM)

RALDH2 siRNA (B) (nM)

-

-

Negative control siRNA (nM)

-

50

-

-

-

5

-

-

10

-

-

30

-

-

50

-

-

-

5

-

-

10

-

-

30

-

-

50

GAPDH

RALDH2

-(-)con50 nM

siRNA(A)

5 nM

siRNA(A)

10 nM

siRNA(A)

30 nM

siRNA(A)

50 nM

GAPDH

RALDH2

-(-)con50 nM

siRNA(B)

5 nM

siRNA(B)

10 nM

siRNA(B)

30 nM

siRNA(B)

50 nM

(Scale bar : 50 μm)

Supplemental Figure II

Se-ries1

0

0.2

0.4

0.6

0.8

1

1.2

1.4

1.6 N1N2N3N4

Me

an

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ld C

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ng

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in g

en

e e

xp

res

sio

n

55 KD

42 KD

Page 3: Marker (%) Normal EPCs Mean ± SM (%) MMD EPCs Mean ± SM (%) CD3426.9 ± 11.531.0 ± 6.8 KDR27.3 ± 5.5222.4 ± 8.90 CD13324.5 ± 4.6412.6 ± 3.93 CD3199.0 ±

GAPDH

RALDH2

-(-)con50 nM

siRNA(A)

50 nM

siRNA(B)

50 nM

A B

C

(Scale bar : 500 μm)

ATRA (-) ATRA 10 μM

Supplemental Figure III(-

) c

on

tro

l s

iRN

AR

AL

DH

2

siR

NA

(A)

RA

LD

H2

siR

NA

(B)

No

n

0

20

40

60

80

100

120

Via

bili

ty (

%)

Nontreated

(-)controlsiRNA

RALDH2siRNA

(A)

RALDH2siRNA

(B)

0

0.2

0.4

0.6

0.8

1

1.2

Mea

n Fo

ld C

hang

e in

gen

e ex

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sion

Nontreated

(-)controlsiRNA

RALDH2siRNA

(A)

RALDH2siRNA

(B)

0

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40

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80

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120

Pro

life

rati

on (

%)

Nontreated

(-)controlsiRNA

RALDH2siRNA

(A)

RALDH2siRNA

(B)

Page 4: Marker (%) Normal EPCs Mean ± SM (%) MMD EPCs Mean ± SM (%) CD3426.9 ± 11.531.0 ± 6.8 KDR27.3 ± 5.5222.4 ± 8.90 CD13324.5 ± 4.6412.6 ± 3.93 CD3199.0 ±

Supplemental Figure I. Phenotypic characterization of endothelial colony forming cells (ECFCs).(A) ECFCs show temporal morphological changes and colonies display a cobblestone morphology. (B) FACS analysis of CD34, KDR, CD133, CD31 and CD45. (C) DiI-labeled Ac-LDL uptake by ECFCs. (D) Immunofluorescence staining of ECFCs labeled with antibodies against CD31 and vWF.  Supplemental Figure II. Retinaldehyde dehydrogenase 2 (RALDH2) knockdown by siRNA transfection in normal endothelial colony forming cells (ECFCs).(A) Visualization of efficient transfection of siRNA into normal ECFCs as green cells. (B) RT-PCR shows effective knockdown of RALDH2 by using two types of siRNA. (C) Similar results from real-time quantitative PCR, demonstrates that the expression of the RALDH2 mRNA is decreased after transfection with siRNA. (D) Gene knockdown was confirmed at the protein level. (N1: normal sample #1, N2: normal sample #2, N3: normal sample #3, N4: normal sample #4) Supplemental Figure III. Effective knockdown retinaldehyde dehydrogenase 2 (RALDH2) and the effect of all-trans retinoic acid (ATRA) treatment on tube formation in human umbilical vein endothelial cell (HUVEC).(A) Normal tube formation capabilities of HUVECs in vitro are inhibited after RALDH2 siRNA was trans-fected. The inhibited tube formation ability of HUVECs after RALDH2 knock down is partially restored after treatment with ATRA. (B) RT-PCR shows effective knock-down of RALDH2 by using 2 types of siRNA in HUVECs. Real-time quantitative PCR also confirms that the expression of RALDH2 mRNA is decreased after transfection with siRNA. (C) The viability and proliferation are not affected by transfection with RALDH2 siRNA.