1
1. INTRODUCTION: Construction of urinary bladder wall de novo for cancer patients with tissue engineering approach disqualify the use of autologous urothelial cells. 2. AIM: The goal of this study was to analyze if adipose derived stem cells (ADSCs) can transdifferentiate into urothelial- like cells (U-LCs) and serve potentially to construct urinary bladder wall in vitro. The present work was supported by the National Center for Research and Development in Poland under Agreement no STRATEGMED1/235368/8/NCBR/2014 (Smart AUCI Project) within the Strategic Programme STRATEGMED “Prevention practices and treatment of civilization diseases” . Adipose derived stemcell s ( ADSCs) HAVE ADIPOSE DERIVED STEM CELLS POTENTIAL TO TRANSDIFFERENTIATE INTO UROTHELIAL CELLS? Buhl M , Rasmus M, Jundzill A, Balcerczyk D, Kloskowski T, Szeliski K, Dąbrowski P, Drewa T, Pokrywczynska M Department of Regenerative Medicine, Nicolaus Copernicus University in Torun, Ludwik Rydygier Medical College in Bydgoszcz, Poland DIFFERENTIATION 7 OR 14 DAYS ADSCs U-LCs? 3. MATERIALS AND METHODS: DIFFERENTIATION: + a standard medium used for ADSCs culture (SM) with the addition of urothelium derived conditioned medium (U-CM) =ADSCs + U-CM 1st NEGATIVE CONTROL (NC): + SM =NC + SM 2nd NEGATIVE CONTROL (NC): SM with the addition of fresh medium used for urothelial cells (UCs) culture (U-FM) =NC + U-FM ADSCs UCs 4. RESULTS - CELL MORPHOLOGY: 0 7 14 ADSCs + U-CM NC + SM NC + U-FM PC+ U-FM 4. REAL-TIME PCR: POSITIVE CONTROL (PC): + the standard, fresh medium used for UCs culture (U-FM) =PC + U-FM A DS Cs+ U-CM NC+SM NC+ S M N C+U-F M PC+U-FM 0 20 40 60 80 100 ADSCs+U-CM N C+ U-FM PC+U-FM 14 days CK8 CK19 CK18 UP1b CD44 CD105 The relative expression 0 20 40 60 80 100 7 days 5. CONCLUSIONS: The study showed that ADSCs have no potential to transdifferentiate into urothelial- like cells and therefore there is a need to improve this method of transdifferentiation or search another type of stem cells to create urothelial cells for construction of urinary bladder wall de novo.

HAVE ADIPOSE DERIVED STEM CELLS POTENTIAL TO ...smartauci.com/pdf/praga.pdf · cells. 2. AIM: The goal of this study was to analyze if adipose derived stem cells (ADSCs) can transdifferentiate

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Page 1: HAVE ADIPOSE DERIVED STEM CELLS POTENTIAL TO ...smartauci.com/pdf/praga.pdf · cells. 2. AIM: The goal of this study was to analyze if adipose derived stem cells (ADSCs) can transdifferentiate

1. INTRODUCTION: Construction of urinary bladder wall de novo for cancer patients with tissue engineering approach disqualify the use of autologous urothelial cells. 2. AIM: The goal of this study was to analyze if adipose derived stem cells (ADSCs) can transdifferentiate into urothelial- like cells (U-LCs) and serve potentially to construct urinary bladder wall in vitro.

The present work was supported by the National Center for Research and Development in Poland under Agreement no STRATEGMED1/235368/8/NCBR/2014 (Smart AUCI Project) within the Strategic Programme STRATEGMED “Prevention practices and treatment of civilization diseases”.

ADSCs+U-CM

NC+SM

NC+U-FM

PC+U-FM

Before the differen�a�on A�er 7 days A�er 14 days

Adipose derived stem cells (ADSCs)

+ a standard medium used for ADSCs culture (SM)

with the addi�on of urothelium derived condi�oned medium (U-CM)

= the differen�a�on (ADSCs + U-CM)

+ SM = the 1st nega�ve control (NC + SM)

+ SM with the addi�on of fresh medium used for UCs culture (U-FM)

= the 2nd NC (NC + U-FM)

HAVE ADIPOSE DERIVED STEM CELLS POTENTIAL TO TRANSDIFFERENTIATE INTO UROTHELIAL CELLS?

Buhl M, Rasmus M, Jundzill A, Balcerczyk D, Kloskowski T, Szeliski K, Dąbrowski P, Drewa T, Pokrywczynska M Department of Regenerative Medicine, Nicolaus Copernicus University in Torun, Ludwik Rydygier Medical College in Bydgoszcz, Poland

DIFFERENTIATION

7 OR 14 DAYS

ADSCs U-LCs?

3. MATERIALS AND METHODS:

DIFFERENTIATION: + a standard medium used for ADSCs culture (SM) with the addition of urothelium derived conditioned medium (U-CM) =ADSCs + U-CM

1st NEGATIVE CONTROL (NC): + SM =NC + SM

2nd NEGATIVE CONTROL (NC): SM with the addition of fresh medium used for urothelial cells (UCs) culture (U-FM) =NC + U-FM

ADSCs

UCs

4. RESULTS - CELL MORPHOLOGY:

0 7 14

AD

SCs

+ U

-CM

N

C +

SM

N

C +

U-F

M

PC

+ U

-FM

4. REAL-TIME PCR:

POSITIVE CONTROL (PC): + the standard, fresh medium used for UCs culture (U-FM) =PC + U-FM

ADSCs+

U-C

M

NC+S

M

NC+S

M

NC+U

-FM

PC+U

-FM

0

20

40

60

80

100

ADSCs+

U-C

M

NC+U

-FM

PC+U

-FM

14 days CK8

CK19

CK18

UP1b

CD44

CD105

Th

e r

ela

tive e

xp

ressio

n

0

20

40

60

80

100 7 days5. CONCLUSIONS: The study showed that ADSCs have no potential to transdifferentiate into urothelial- like cells and therefore there is a need to improve this method of transdifferentiation or search another type of stem cells to create urothelial cells for construction of urinary bladder wall de novo.